2011
- Stabilization of Excited State Using Through-Space Interaction between Independent π-Systems Mediated by a peri-Substituted Hydroxy Group in 1-Arylnaphthalenes: Unexpected Blue Emission of 1,3,5-Tris(peri-hydroxynaphthyl)benzene [abstract]
Hideto Nakajima, Makoto Yasuda, Kenji Shimizu, Naomi Toyoshima, Yasunori
Tsukahara, Takao Kobayashi, Shinichiro Nakamura, Kouji Chiba, and Akio
Baba
Bull. Chem. Soc. Jpn. 2011, 84, 1118-1129.
- InI3/Me3SiI-catalyzed Direct Alkylation of Enol Acetates Using Alkyl Acetates or
Alkyl Ethers [abstract]
Yoshiharu Onishi, Yoshihiro Nishimoto, Makoto Yasuda, Akio Baba
Chem. Lett. 2011, 40, 1223-1225.
- Direct Synthesis of Alkynylstannanes: ZnBr2 Catalyst for the Reaction of
Tributyltin Methoxide and Terminal Alkynes [abstract]
Kensuke Kiyokawa, Nodoka Tachikake, Makoto Yasuda, Akio Baba
Angew. Chem. Int. Ed. 2011, 50, 10393-10396.
- Carbogallation of Alkynes Using Gallium Tribromide and Silyl Ketene Acetals and Synthetic Application to Cross-Coupling with Aryl Iodides [abstract]
Yoshihiro Nishimoto, Hiroki Ueda, Makoto Yasuda, Akio Baba
Chem. Eur. J. 2011, 17, 11135-11138.
- Indium Tribromide Catalyzed Cross-Claisen Condensation between Carboxylic
Acids and Ketene Silyl Acetals Using Alkoxyhydrosilanes [abstract]
Yoshihiro Nishimoto, Aya Okita, Makoto Yasuda, Akio Baba
Angew. Chem. Int. Ed. 2011, 50, 8623-8625.
- InCl3/Me3SiBr-Catalyzed Direct Coupling between Silyl Ethers and Enol Acetates [abstract]
Yoshiharu Onishi, Yoshihiro Nishimoto, Makoto Yasuda, Akio Baba
Org. Lett. 2011, 13, 2762-2765.
- Substituted Butenylindium Generated by Transmetalation of Cyclopropylmethylstannane
with Indium Iodide: Synthesis and Characterization of Monobutenylindium [abstract]
Kensuke Kiyokawa, Makoto Yasuda, and Akio Baba
Organometallics, 2011, 30, 2039-2043.
- Cage-Shaped Borate Esters with Tris(2-oxyphenyl)methane or ‒silane System Frameworks Bearing Multiple Tuning Factors: Geometric and Substituent Effects on Their Lewis Acid Properties [abstract]
Makoto Yasuda, Hideto Nakajima, Ryosuke Takeda, Sachiko Yoshioka, Satoshi Yamasaki, Kouji Chiba, Akio Baba
Chem. Eur. J. 2011, 17, 3856-3867.
- Synthesis of Cyclopropane-Containing Phosphorus Compounds by Radical Coupling
of Butenylindium with Iodo Phosphorus Compounds [abstract]
Kensuke Kiyokawa, Itaru Suzuki, Makoto Yasuda, Akio Baba
Eur. J. Org. Chem. 2011,2163-2171.
- Highly efficient synthesis of cyclic carbonates from epoxides catalyzed
by indium tribromide system [abstract]
Ikuya Shibata, Ikuko Mitani, Akira Imakuni, and Akio Baba
Tetrahedron Lett. 2011, 52, 721-723.
|
2010
- Diastereoselective Reductive Aldol Reaction of Enones to Ketones Catalyzed
by Halogenotin Hydride [abstract]
Ikuya Shibata, Shinji Tsunoi, Kumiko Sakabe, Shinji Miyamoto, Hirofumi
Kato, Hideto Nakajima, Makoto Yasuda, and Akio Baba
Chem. A-Eur. J. 2010, 16, 13335-13338.
-
Novel catalysts: Indium implanted SiO2 thin films [abstract]
S. Yoshimura, K. Hine, M. Kiuchi, Y. Nishimoto, M. Yasuda, A. Baba and
S. Hamaguchi
Applied Surface Science 2010, 257, 192-196.
-
Characterization of the Nucleophilic Allylindium Species Generated from Allyl Bromide and Indium(0) in Aqueous Media [abstract]
Makoto Yasuda,Masahiko Haga,Yasunori Nagaoka,Akio Baba
Eur. J. Org. Chem. 2010, 28, 5359-5363.
-
Regioselective Carboindation of Simple Alkenes with Indium Tribromide and
Ketene Silyl Acetals [abstract]Yoshihiro Nishimoto, Hiroki Ueda, Yoshihiro Inamoto, Makoto Yasuda and
Akio Baba
Org. Lett., 2010, 12, 3390–3393.
- Synthesis
and theoretical studies of gallium complexes back-shielded by a
cage-shaped framework of tris(m-oxybenzyl)arene [abstract]
Hideto Nakajima, Makoto Yasuda, Kouji Chiba and Akio Baba,
Chem Commun. 2010, 46, 4794 - 4796
- Indium Triiodide Catalyzed Direct Hydroallylation of Esters [abstract]
Yoshihiro Nishimoto, Yoshihiro Inamoto, Takahiro Saito, Makoto Yasuda,
Akio Baba
Eur. J. Org. Chem. 2010, 3382–3386
- In Situ Observation of Nonequilibrium Local Heating as an Origin of Special Effect of Microwave on Chemistry[abstract]
Yasunori Tsukahara, Ayano Higashi, Tomohisa Yamauchi, Takashi Nakamura,
Makoto Yasuda, Akio Baba and Yuji Wada
J. Phys. Chem. C, 2010, 114 (19), 8965–8970.
- Cyclopropylmethylation of Benzylic and Allylic Chlorides with
Cyclopropylmethylstannane Catalyzed by Gallium or Indium Halide [abstract]
Kensuke Kiyokawa, Makoto Yasuda and Akio Baba
Org. Lett. 2010, 12, 1520-1523.
.
|
2009
- Radical Coupling of Iodocarbonyl Compounds with Butenylindium Generated
by Transmetalation between Cyclopropylmethylstannane and Indium Halides [abstract]
Makoto Yasuda, Kensuke Kiyokawa, Kenji Osaki and Akio Baba
Organometallics, 2009, 28 (1), 132–139.
- Highly stereoselective synthesis of vicinal diols by stannous chloride-mediated
addition of hydroxyallylic stannanes to aldehydes [abstract]
Makoto Yasuda, Tatsuya Azuma, Kensuke Tsuruwa, Srinivasarao Arulananda
Babu and Akio Baba
Tetrahedron Lett. 2009, 50, 3209–3212.
- Isolation and Characterization of a Nucleophilic Allylic Indium Reagent [abstract]
Makoto Yasuda, Masahiko Haga and Akio Baba
Organometallics, 2009, 28 (7), 1998–2000.
- Regio- and Stereoselective Generation of Alkenylindium Compounds from Indium
Tribromide, Alkynes, and Ketene Silyl Acetals [abstract]
Yoshihiro Nishimoto, Ryosuke Moritoh, Makoto Yasuda, Akio Baba
Angew. Chem. Int. Ed. 2009, 48, 4577 –4580.
- Indium-catalyzed coupling reaction between silyl enolates and alkyl chlorides
or alkyl ethers [abstract]
Yoshihiro Nishimoto, Takahiro Saito, Makoto Yasuda and Akio Baba
Tetrahedron, 2009, 65, 5462-5471.
- Isolation and Crystallographic Characterization of Allylindium Species
Generated from Allyl Halide and Indium(0) [abstract]
Makoto Yasuda, Masahiko Haga, Akio Baba
Eur. J. Org. Chem. 2009, 5513-5517.
- Stereoselective synthesis of vicinal diols by the stannous chloride-mediated
reaction of unprotected hydroxyallylic stannane with carbonyl compounds [abstract]
Makoto Yasuda, Kensuke Tsuruwa, Tatsuya Azuma, Srinivasarao Arulananda
Babu, Akio Baba
Tetrahedron. 2009, 65, 9569–9574.
- α-Alkylation of Carbonyl Compounds by Direct Addition of Alcohols to Enol
Acetates
Yoshihiro Nishimoto, Yoshiharu Onishi, Makoto Yasuda, Akio Baba [abstract]
Angew. Chem., Int. Ed. 2009, 48, 9131-9134.
|
2008
- Fine-Tuning of Boron Complexes with Cage-Shaped Ligand Geometry: Rational
Design of Triphenolic Ligand as a Template for Structure Control [abstract]
Makoto Yasuda, Sachiko Yoshioka, Hideto Nakajima, Kouji Chiba, and Akio
Baba
Org. Lett. 2008, 10(5), 929-932.
- Bu2SnIH-Promoted Proximal Bond Cleavage of Methylenecyclopropanes and Successive
Radical Cyclization and/or Pd-Catalyzed Coupling Reaction [abstract]
Naoki Hayashi, Yusuke Hirokawa, Ikuya Shibata, Makoto Yasuda, and Akio
Baba
J. Am. Chem. Soc. 2008, 130 (10), 2912 -2913.
- Reaction of alcohols and silyl ethers in the presence of an indium/silicon-based
catalyst system: Deoxygenation and allyl substitution [abstract]
Akio Baba, Makoto Yasuda, Yoshihiro Nishimoto, Takahiro Saito, and Yoshiyuki
Onishi
Pure Appl. Chem. 2008, 80, 845-854.
- Regiocontrolled Addition of Carbonyl Compounds with Allylic Indium Generated
by Hydroindation of 1,3-Dienes [abstract]
Naoki Hayashi, Hiroyuki Honda, Ikuya Shibata, Makoto Yasuda, Akio Baba
Synlett 2008, 1407-1411.
- Microwave-Irradiated Transition-Metal Catalysis: Rapid and Efficient Dehydrative
Carbon-Carbon Coupling of Alcohols with Active Methylenes [abstract]
Srinivasarao Arulananda Babu, Makoto Yasuda, Yasunori Tsukahara, Tomohisa
Yamauchi, Yuji Wada, Akio Baba
Synthesis 2008, 1717-1724.
- Hydroindation of allenes and its application to radical cyclization [abstract]
Naoki Hayashi, Yusuke Hirokawa, Ikuya Shibata, Makoto Yasuda and Akio Baba
Org. Biomol. Chem. 2008, 6, 1949 - 1954.
- Direct chlorination of alcohols with chlorodimethylsilane catalyzed by
a gallium trichloride/tartrate system under neutral conditions [abstract]
Makoto Yasuda, Kenji Shimizu, Satoshi Yamasaki and Akio Baba
Org. Biomol. Chem. 2008, 6, 2790-2795.
- Germanium(II)-Mediated Reductive Cross-Aldol Reaction of Bromoaldehydes
with Aldehydes: NMR Studies and ab Initio Calculations [abstract]
Shin-ya Tanaka, Nobuo Tagashira, Kouji Chiba, Makoto Yasuda, and Akio Baba.
J. Org. Chem., 2008, 73, 6312-6320.
- Germanium(II)-Mediated Reductive Mannich-Type Reaction of α-Bromoketones
to N-Alkylimines [abstract]
Shin-ya Tanaka, Nobuo Tagashira, Kouji Chiba, Makoto Yasuda, and Akio Baba
Angew. Chem. Int. Ed., 2008, 47, 6620-6623.
- Direct coupling of alcohols with alkenylsilanes catalyzed by indium trichloride
or bismuth tribromide [abstract]
Yoshihiro Nishimoto, Masayuki Kajioka, Takahiro Saito, Makoto Yasuda and
Akio Baba
Chem. Commun., 2008, 6396-6398.
- Esters as Acylating Reagent in a Friedel-Crafts Reaction: Indium Tribromide
Catalyzed Acylation of Arenes Using Dimethylchlorosilane [abstract]
Yoshihiro Nishimoto, Srinivasarao Arulananda Babu, Makoto Yasuda and Akio
Baba
J. Org. Chem., 2008, 73 (23), 9465-9468
|
2007
- One-Pot Synthesis of Heterocyclic Compounds Initiated by Chemoselective
Addition of b-Acyl Substituted Unsaturated Aldehydes with Nucleophilic
Tin Complexes
I. Shibata, H. Kato, M. Yasuda, A. Baba
J. Organomet. Chem. 2007, 692, 604-619.
- In(III)-Mediated Chemoselective Dehydrogenative Interaction of ClMe2SiH with Carboxylic Acids: Direct Chemo- and Regioselective Friedel-Crafts
Acylation of Aromatic Ethers
Srinivasarao Arulananda Babu, Makoto Yasuda, and Akio Baba.
Org. Lett. 2007, 9, 405-408.
- Germanium(II)-Mediated Reductive Cross-Aldol Reaction of Aldehydes: Synthesis
of Aldols withDiastereocontrolled Quaternary Carbon Centers
Shin-ya. Tanaka, M. Yasuda, A. Baba
Synlett 2007, 1720-1724.
- Regio- and stereoselective hydrostannation of allenes using dibutyliodotin
hydride (Bu2SnIH) and successive coupling with aromatic halides
Naoki Hayashi, Kazunao Kusano, Shingo Sekizawa, Ikuya Shibata, Makoto Yasuda
and Akio Baba
Chem. Commun. 2007, 4913-4915
- InCl3/I2-Catalyzed Cross-Coupling of Alkyl Trimethylsilyl Ethers and Allylsilanes
via an in Situ Derived Combined Lewis Acid of InCl3 and Me3SiI
Saito, T.; Nishimoto, Y.; Yasuda, M.; Baba, A.
J. Org. Chem. 2007, 72, 8588-8590.
- Coupling Reaction of Alkyl Chlorides with Silyl Enolates Catalyzed by Indium
Trihalide
Yoshihiro Nishimoto, Makoto Yasuda, and Akio Baba
Org. Lett. 2007, 9(24), 4931-4934
- Diastereoselective Production of Homoallylic Alcohols Bearing Quaternary
Centers from γ-Substituted Allylic Indiums and Ketones [abstract]
Srinivasarao Arulananda Babu, Makoto Yasuda, and Akio Baba
J. Org. Chem. 2007, 72, 10264-10267
|
2006
- Direct Chlorination of Alcohols: Synthesis of Ethyl 3-Chloro-3-Phenylpropanoate
[Benzenepropanoic acid, b-chloro-, ethyl ester]
Yasuda, M.; Yamasaki, S.; Onishi, Y.; Baba A.
Org. Synth. 2006, 83, 38-44.
- Direct Carbon-Carbon Bond Formation from Alcohols and Active Methylenes,
Alkoxyketone, or Indoles Catalyzed by Indium Trichloride without Salt Formation
Yasuda, M.; Somyo, T.; Baba A.
Angew. Chem., Int. Ed. 2006, 45, 793-796.
- Practical and Simple Synthesis of Substituted Quinolines by an HCl-DMSO
System on a Large Scale: Remarkable Effect of the Chloride Ion
Tanaka, S.; Yasuda, M.; Baba A.
J. Org. Chem. 2006, 71, 800-803.
- One-pot Synthesis of Heterocycles Initiated by Chemoselective Reduction
of Bifunctional Carbonyl Compounds
Kato, H.; Shibata, I.; Kanazawa, N.; Yasuda, M.;. Baba A.
Eur. J. Org. Chem. 2006. 1117-1120.
- Cage-Shaped Borate Esters with Enhanced Lewis Acidity and Catalytic Activity
Makoto Yasuda, Sachiko Yoshioka, Satoshi Yamasaki, Toshio Somyo, Kouji
Chiba, and Akio Baba
Org. Lett. 2006, 8, 761-764.
- High Chelation Control of Three Contiguous Stereogenic Centers in the Reformatsky
Reaction of Indium Enolates with a-Hydroxy Ketones: Unexpected Stereochemistry
of Lactone Formation
Babu, S. A.; Yasuda, M.; Okabe, Y.; Shibata, I.; Baba, A.
Org. Lett. 2006, 8, 3029-3032.
- The Reductive Amination of Aldehydes and Ketones by Catalytic Use of Dibutylchlorotin
Hydride Complex
Kato, H.; Shibata, I.; Yasaka, Y.; Tsunoi, S.; Yasuda, M.; Baba, A.
Chem. Commun. 2006, 4189-4191.
- Generation of Allylic Indium by Hydroindation of 1,3-Dienes and One-Pot
Reaction with Carbonyl Compounds
Hayashi, N.; Honda, H.; Yasuda, M.; Shibata, I.; Baba, A.
Org. Lett. 2006, 8, 4553-4556.
- Direct Coupling Reaction between Alcohols and Silyl Compounds: Enhancement
of Lewis Acidity of Me3SiCl Using InCl3
T. Saito, Y. Nishimoto, M. Yasuda, A. Baba
J. Org. Chem. 2006, 71, 8516-8522.
|
2005
- Reductive Cross-Aldol Reaction Using Bromoaldehyde and an Aldehyde Mediated
by Germanium(II): One-Pot, Large-Scale Protocol
Yasuda, M.; Tanaka, S.; Baba A.
Org. Lett. 2005, 7, 1845-1848.
- Indium-Silicon Combined Lewis Acid Catalyst for Direct Allylation of Alcohols
with Allyltrimethylsilane in Non-Halogenated Solvent
Saito, T.; Yasuda, M.; Baba A.
Synlett, 2005, 1737-1739.
- Michael addition of ketone enolates to a,b-unsaturated esters or amides
in a one-pot procedure: Highly efficient effect of lithium salt generated
in situ on organotin enolate.
Yasuda, M.; Shigeyoshi, Y.; Shibata, I.;. Baba A
Synthesis, 2005, 233-239.
- Inter- and Intramolecular Radical Couplings of Ene-ynes or Halo-alkenes
Promoted by an InCl3/MeONa/Ph2SiH2 System.
Hayashi, N.; Shibata, I.; Baba A.
Org. Lett. 2005, 7, 3093-3096.
- Dihaloindium Hydride as Novel Reducing Agents
Baba, A.; Shibata I.
The Chemical Record, 2005, 5, 323-335.
- In-or In(I)-Employed Tailoring of the Stereogenic Centers in the Reformatsky-Type
Reactions of Simple Ketones, a-Alkoxy Ketones and b-Keto Esters
Babu, S. A.; Yasuda, M.; Shibata, I.; Baba A.
J. Org. Chem. 2005, 70, 10408-10419.
|
2004
- Synthesis of 2-Monosubstituted Pyrroles by Intramolecular Addition of Amines
via Reductive Amination with Dibutyliodotin Hydride Complex (Bu2SnIH-HMPA)
Ikuya Shibata, Hirofumi Kato, Nobuaki Kanazawa, Makoto Yasuda and Akio
Baba
Synlett, 2004, 137-139
- Catalytic Generation of Indium Hydride and Highly Diastereoselective Reductive
Aldol Reaction
Ikuya Shibata, Hirofumi Kato, Tatsuya Ishida, Makoto Yasuda and Akio Baba
Angew. Chem. Int. Ed. 2004, 43(6), 711-714.
- Direct Substitution of the Hydroxyl Group in Alcohols with Silyl Nuculeophiles
Catalyzed by Indium Trichloride
Makoto Yasuda, Takahiro Saito, Masako Ueba, and Akio Baba
Angew. Chem. Int. Ed. 2004, 43, 1414-1416
- Allylic Tantalums as Highly Imine-selective Reagents
Ikuya Shibata, Kyo Nose, Makoto Yasuda and Akio Baba
J. Org. Chem. 2004, 69, 2185-2187
- One-pot Synthesis of Nitrogen Heterocycles Initiated by Regio- and
Diastereoselective Carbon-Carbon Bond Formation of Bifunctional Carbonyl
Compounds
Ikuya Shibata, Hirofumi Kato, Nobuaki Kanazawa Makoto Yasuda and Akio Baba
J. Am. Chem. Soc. 2004, 126(2), 466-467
- Indium-Employed One-Pot Sequential Double Nucleophilic Attack on a Symmetrical
DicarboxaldehydeSrinivasarao
Arulananda Babu, Makoto Yasuda, Ikuya Shibata, and Akio Baba
Synlett, 2004, 1223-1226.
- Indium-Catalyzed Direct Chlorination of Alcohols Using Chlorodimethylsilane-Benzil
as a Selective and Mild System
Makoto Yasuda, Satoshi Yamasaki, Yoshiyuki Onishi, and Akio Baba
J. Am. Chem. Soc. 2004, 126, 7186-7187
- In- or In(I)-Employed DiastereoselectiveReformatsky-Type Reactions withKetones:
1H NMR Investigations on theActive Species
Srinivasarao Arulananda Babu, Makoto Yasuda, Ikuya Shibata, and Akio Baba*
Org. Lett. 2004, 6(24), 4475-4478.
- Triethylsilane-Indium(III) Chloride System as a Radical Reagent
Naoki Hayashi, Ikuya Shibata, and Akio Baba*
Org. Lett. 2004, 6(26), 4981-4983.
|
2003
- Michael Addition of Stannyl Ketone Enolate to a,b-Unsaturated Esters Catalyzed
by Tetrabutylammonium Bromide and an ab Initio Theoretical Study on the
Reaction Course
Makoto Yasuda, Kouji Chiba, Noriyuki Ohigashi, Yasuhiro Katoh, and Akio
Baba
J. Am. Chem. Soc. 2003, 125, 7291 - 7300.
|
2002
- Direct Conversion of Carbonyl Compounds into Organic Halides: Indium(III)
Hydroxide-Catalyzed Deoxygenative Halogenation Using Chlorodimethylsilane.
Yoshiyuki Onishi, Daigo Ogawa, Makoto Yasuda, Akio Baba
J. Am. Chem. Soc. 2002, 124, 13690-13691.
- Diastereoselective Addition of gamma-Substituted Allylic Nucleophiles to
Ketones: Highly Stereoselective Synthesis of Tertiary Homoallylic Alcohols
Using an Allylic Tributylstannane/Stannous Chloride System
Makoto Yasuda, Kay Hirata, Mitsuyoshi Nishino, Akihiro Yamamoto, Akio Baba
J. Am. Chem. Soc. 2002, 124, 13442-13447.
- Indium(III) Chloride/Chlorotrimethylsilane as a Highly Active Lewis Acid
Catalyst System for the Sakurai-Hosomi Reaction
Yoshiyuki Onishi, Takeshi Ito, Makoto Yasuda, Akio Baba,
Eur. J. Org. Chem. 2002, 1578-1581.
- Remarkable enhancement of Lewis acidity of chlorosilane by the combination
use of indium(III) chloride
Yoshiyuki Onishi, Takeshi Ito, Makoto Yasuda, Akio Baba,
Tetrahedron, 2002, 58, 8227-8235.
- Cross-Coupling Reaction of alpha-Chloroketones and Organotin Enolates Catalyzed
by Zinc Halides for Synthesis of gamma-Diketones
Makoto Yasuda, Shoki Tsuji, Yusuke Shigeyoshi, Akio Baba
J. Am. Chem. Soc. 2002, 124(25), 7440-7447.
- Generation of Organotantalum Reagents and Conjugate Addition to Enones
Ikuya Shibata, Takeyoshi Kano, Nobuaki Kanazawa, Shoji Fukuoka, and Akio
Baba
Angew. Chem. Int. Ed. Eng. 2002, 41(8), 1389-1392.
- Indium Chloride-Sodium Borohydride System: A Convenient Radical Reagent
for an Alternative to Tributyltin Hydride System
Katsuyuki Inoue, Akemi Sawada, Ikuya Shibata, Akio Baba
J. Am. Chem. Soc. 2002, 124(6), 906-907.
- Remarkable Dependence of Diastereoselectivity on Anhydrous- or Aqueous
Solvent in the Indium Hydride Promoted Reductive Aldol Reaction of alpha,
beta-Unsaturated Ketones
Katsuyuki Inoue, Tatsuya Ishida, Ikuya Shibata and Akio Baba
Adv. Synth. Catal. 2002, 344(Water-Issue)(3+4), 283-287.
- Ionic Activation of Tin Hydrides
Ikuya Shibata and Akio Baba
Curr. Org. Chem. 2002, 6(8), 665-693.
- Highly Diastereoselective Reformatsky-Type Reaction Promoted by Tin Iodide
Ate Complex
Ikuya Shibata, Toshihiro Suwa, Hideaki Sakakibara and Akio Baba
Org. Lett. 2002, 4(2), 301-303.
|
2001
- 高配位化手法を機軸とした有機スズエノラートを用いる新しい合成反応;
安田 誠、馬場章夫;
有機合成化学協会誌, 2001, 59, 697-706.
- Synthetic Application of a Series of Organotin Hydride;
Ikuya Shibata, Akio Baba;
Main Group Metal Chemistry, 2001, 24, 637-646.
- Indium(III) Chloride-Catalyzed Coupling Reaction of Acid Chlorides and
Allylic Tins;
Katsuyuki Inoue, Yasuhiro Shimizu, Ikuya Shibata, Akio Baba;
Synlett, 2001, 1659-1661.
- A Highly syn-Selective Allylation of Aldehydes in Water;
Ikuya Shibata, NaritoshiYoshimura, Masahiro Yabu, Akio Baba;
Eur. J. Org. Chem., 2001, 3207-3211.
- Indium Hydride; A Novel Radical Initiator in the Reduction of Organic Halides
with Tributyltin Hydride;
Katsuyuki Inoue, Akemi. Sawada, Ikuya Shibata, Akio Baba;
Tetrahedron Lett., 2001, 42, 4661-4663.
- Selective a-Stannylated-Addition of Di-n-butyliodotin Hydride Ate Complex
to Simple Aliphatic Alkynes;
Ikuya Shibata, Toshihiro Suwa, Kyoichiro Ryu, Akio Baba;
J. Am. Chem. Soc., 2001, 123, 4101-4102.
- Highly Stereoselective Addition to Alkoxy or Hydroxy Ketones Using an a-Stannyl
Ester-Stannous Chloride System in a Chelation-Controlled Manner;
Makoto Yasuda, Keishi Okamoto, Toshiyuki. Sako, Akio Baba ;
Chem. Commun., 2001, 157-158.
- Direct Reduction of Alcohols. Highly Chemoselective Reducing System for
Secondary or Tertiary Alcohols Using Chlorodiphenylsilane with a Catalytic
Amount of Indium Trichloride ;
Makoto Yasuda, Yoshiyuki Onishi, Masako Ueba, Takashi Miyai, and Akio Baba;
J. Org. Chem., 2001, 66, 7741-7744.
- Conjugate Hydrostannation of Unsaturated Esters by Iodotin Hydride Ate
Complex;
Ikuya Shibata, Toshihiro Suwa, Kyoichiro Ryu and Akio Baba;
J. Org. Chem., 2001, 66, 8690-8692.
|
2000
- Selective Reduction of Acid Chloride with a Catalytic Amount of an Indium
Compound
K. Inoue, M. Yasuda, I. Shibata, A. Baba
Tetrahedron Lett. 2000, 41, 113-116.
- Reductive Amination Promoted by Tributyltin Hydride
T. Suwa, E. Sugiyama, I. Shibata, A. Baba
Synlett, 2000, 556-558.
- Indium Compound-Catalyzed Deoxygenative Allylation of Aromatic Ketones
by a Hydrosilane-Allylsilane System
M. Yasuda, Y. Onishi, T. Ito, A. Baba
Tetrahedron Lett. 2000, 41, 2425-2428.
- Synthesis of Carbocycles by Enone-selective Reduction using Organoiodotin
Hydride
T. Suwa, K. Nishino, M. Miyatake, I. Shibata, A. Baba
Tetrahedron Lett. 2000, 41, 3403-3406.
- Chemoselective Reductive Amination of Aldehydes and Ketones by Dibutylchlorotin
Hydride-HMPA Complex
T. Suwa, E. Sugiyama, I. Shibata, A. Baba
Synthesis, 2000, 789-800.
- An ab Initio Computational Study on the Reaction of Organotin Enolates:
Comparison of Highly Coordinated Tin Reagent with Noncoordinated Reagent
M. Yasuda, K. Chiba, A. Baba
J. Am. Chem. Soc. 2000, 122, 7549-7555.
- Remarkable Enhancement of Nucleophilicity of Tin Enolates toward Nitro-
or Cyanoalkenes by Tetrabutylammonium Halides
M. Yasuda, N. Ohigashi, A. Baba
Chem. Lett., 2000, 1266-1267.
- Highly Regioselective Addition of an Ester Enolate Equivalent to a,b-Unsaturated
Ketones: Selective Formation of Both Isomers Derived from 1,2- and 1,4-Additions
Using a-Stannyl Ester with Additives
M. Yasuda, Y. Matsukawa, K. Okamoto, T. Sako, N. Kitahara, A. Baba
Chem. Commun., 2000, 2149-2150.
|
1999
- A New Halogen-Exchange between Sn-F and Li-X: Selective 1,2- and 1,4-Reductions
of a,b-Unsaturated Ketones and Effects of Halogen Substituents on the Regioselectivity
of Organotin Hydrides
T. Moriuchi-Kawakami, H. Matsuda, I. Shibata, M. Miyatake, T. Suwa, A.
Baba
Bull. Chem. Soc. Jpn. 1999, 72, 465-470.
- Novel Reductive Fridel-Crafts Alkylation of Aromatics Catalyzed by Indium
Compounds: Chemoselective Utilization of Carbonyl Moieties as Alkylating
Reagents
T. Miyai, Y. Onishi, A. Baba
Tetrahedron, 1999, 55, 1017-1026.
- Novel Synthetic Usage of Indium Compounds as Catalyst: Reductive Deoxygenation
of Aryl Ketones and sec-Benzylic Alcohols
T. Miyai, M. Ueba, A. Baba
Synlett, 1999, (2), 182-184.
- The First Michael Addition of Metal Ketone Enolates to a,b-Unsaturated
Esters under Catalytic Conditions: Tin Enolate with a Catalytic Amount
of Tetrabutylammonium Bromide
M. Yasuda, N. Ohigashi, I. Shibata, A. Baba
J. Org. Chem. 1999, 64 (7) 2180-2181.
- Highly Diastereoselective Aldol Synthesis from a-Iodo Ketones in Aqueous
Media
I. Shibata, M. Kawasaki, M. Yasuda, A. Baba
Chem. Lett. 1999, 689-690.
- Synthesis of a Novel Ate Tin Hydride Complex Bearing a Nucleophilic Iodide
Substituent and 1,4-Regioselective Reduction of a,b-Unsaturated Aldehydes
T. Suwa, I. Shibata, A. Baba
Organometallics, 1999, 18(20) 3965-3967.
- Synthesis of Nitrogen Heterocycles by Intramolecular Michael Type of Amination
via Reduction of Imines with Di-n-butyliodotin Hydride (n-Bu2SnIH)
T. Suwa, I. Shibata, K. Nishino, A. Baba
Org. Lett. 1999, 1(10) 1579-1581.
- Synthetic Applications of Coordinated TIN Enolates and TIN Hydrides
A. Baba, I. Shibata, M. Yasuda
Phosphorus, Sulfur and Silicon, 1999, 150-151, 293-298.
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1998
- Halogen Substituted Tin Hydride System for Chemo-, Regio-, and Stereocontrolled
Reductions
I. Shibata, A. Baba
Reviews on Heteroatom Chemistry, 1998, 18, 247-275.
- Chemoselective Reduction of Imino Groups by Dibutyltin Chloride Hydride
Complex
I. Shibata, T. Moriuchi-Kawakami, D. Tanizawa, T. Suwa, E. Sugiyama, H.
Matsuda, A. Baba
J. Org. Chem. 1998, 63(2), 383-385.
- Highly Controlled Chemoselectivity of Tin Enolate by Its Hybridization
State. Anionic Complex of Tin Enolate Coordinated by Tetrabutylammonium
Bromide as Halo Selective Reagent
M. Yasuda, K. Hayashi, Y. Katoh, I. Shibata, A. Baba
J. Am. Chem. Soc. 1998, 120(4), 715-721.
- Control of Both Syn and Anti Stereoselectivity in Michael Additions of
Organotin Enolates
I. Shibata, K. Yasuda, Y. Tanaka, M. Yasuda, A. Baba
J. Org. Chem. 1998, 63(4), 1334-1336.
- A New Type of Allylation: Synthesisi of b,g-Unsaturated Ketones from a-Halogenated
Aryl Ketones Using an Allyltributyltin(IV)-Tin(II) Dichloride-Acetonitrile
System
M. Yasuda, M. Tsuchida, A. Baba
Chem. Commun. 1998, 563-564.
- Preparation of a Novel Indium Hydride and Application to Practical Organic
Synthesis
T. Miyai, K. Inoue, M. Yasuda, I. Shibata, A. Baba
Tetrahedron Lett. 1998, 39, 1929-1932.
- 有機スズヒドリドの機能制御に基づく官能基、立体および位置選択的還元反応
芝田育也、馬場章夫
有機合成化学協会誌 1998, 56, 280-290.
- Simple Synthetic Method of Allyl- and Vinly-Epoxides by Allylation of Carbonyl
Groups with Allylic Tins Catalyzed by PbI2-HMPA
I. Shibata, S. Fukuoka, A. Baba
Chem. Lett. 1998, 533-534.
- Allylation of Unactivated Ketones by Tetraallyltin Accelerated by Phenol.
Application to Asymmetric Allylation Using a Tetraallyltin-BINOL System
M. Yasuda, N. Kitahara, T. Fujibayashi, A. Baba
Chem. Lett. 1998, 743-744.
- Indium Trichloride Catalyzed Reductive Friedel-Crafts Alkylation of Aromatics
Using Carbonyl Compounds
T. Miyai, Y. Onishi, A. Baba
Tetrahedron Lett. 1998, 39, 6291-6294.
- Allylation of Carbonyl Compounds Bearing a Hydroxyl Group by Tetraallyltin:
Highly Stereoselective Allylation in a Chelation-Controlled Manner
M. Yasuda, T. Fujibayashi, A. Baba
J. Org. Chem. 1998, 63(18), 6401-6404.
- Dibutyltin Chloride Hydride Complex as a Novel Reductant for Chemoselective
Redutive Amination
I. Shibata, T. Suwa, E. Sugiyama, A. Baba
Synlett, 1998, 1081-1082.
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1997
- Selective Reactions of Organotin(IV) Enolates Using High-Coordination Method
Makoto Yasuda, Ikuya Shibata, Akio Baba, Haruo Matsuda
Recent Research Developments in Pure & Applied Chemistry, 1997, 1, 55-71.
- Organotin(IV) Enamines as Selective Reagents: Coupling with a-Halocarbonyls
for Synthesis of Substituted Pyrroles
M. Yasuda, J. Morimoto, I. Shibata, A. Baba
Tetrahedron Lett. 1997, 38(18), 3265-3266.
- Lead Iodide-HMPA as a Novel Catalyst for Chemo- and Diastereoselective
Carbonyl Allylation of a,b-Epoxy Ketones with Allylic Stannanes
I. Shibata, S. Fukuoka, N. Yoshimura, H. Matsuda, A. Baba
J. Org. Chem. 1997, 62(12), 3790-3791.
- Indium Triiodide(InI3)-Catalyzed Allylation of Carbonyl Compounds by Allylic Tins
T. Miyai, K. Inoue, M. Yasuda, A. Baba
Synlett, 1997, 6, 699-700.
- Synthesis of 1,4-Diketones: Unusual Coupling of Tin Enolates with a-Chloroketones
Catalyzed by Zinc Halides
M. Yasuda, S. Tsuji, I. Shibata, A. Baba
J. Org. Chem. 1997, 62(24), 8282-8283.
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1996
- NMR Studies of Three Types of Highly Coordinated Organotin Hydrides: Chemo-,
Regio-, and Stereoselective Reduction of 2,3-Epoxy Ketones
T. Kawakami, I. Shibata, A. Baba
J. Org. Chem. 1996, 61(1), 82-87.
- Organotin Iodide Hydride: Chemoselective 1,4-Hydrostannations of Conjugated
Enones in the Presence of Aldehydes and Subsequent Intermolecular Aldol
Reactions
T. Kawakami, M. Miyatake, I. Shibata, A. Baba
J. Org. Chem. 1996, 61(1), 376-379.
- Allylic Tin(IV)-Tin(II) Chloride-Acetonitrile as a Novel System for Allylation
of Carbonyls or Imines
M. Yasuda, Y. Sugawa, A. Yamamoto, I. Shibata, A. Baba
Tetrahedron Lett. 1996, 37(33), 5951-5954.
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1995
- Chlorotrimethylsilane-Acetonitrile Sysytem as a New Promoter for Carbonyl
Allylation by Diallyldibutyltin
M. Yasuda, T. Fujibayashi, I. Shibata, A. Baba, H. Matsuda, N. Sonoda
Chem. Lett. 1995, 167, 167-168.
- Catalytic Effect of Five-Coordinate Organotin Bromide or Tetraphenylstibonium
Bromide on the Chemo- and Stereoselective Addition of Tin Enolate to a-Halo
Ketone
M. Yasuda, T. Oh-hata, I. Shibata, A. Baba, H. Matsuda, N. Sonoda
Bull. Che. Soc. Jpn. 1995, 68(4), 1180-1186.
- Highly Coordinated Tin Hydrides: A Novel Synthesis of Tertiary Amines via
Hydrostannation of Imines
T. Kawakami, T. Sugimoto, I. Shibata, A. Baba, H. Matsuda, N. Sonoda
J. Org. Chem. 1995, 60, 2677-2682.
- Chemo- and Regioselective Reductions of Functionalized Epoxides by Bu3SnH/Bu3SnI Phosphine Oxide
T. Kawakami, D. Tanizawa, I. Shibata, A. Baba
Tetrahedron Lett. 1995, 36(51), 9357-9360.
- Solvent-Controlled Addition of Alkynyltins or Allylic Tins to Aldehydes
Catalyzed by Indium Trichloride
M. Yasuda, T. Miyai, I. Shibata, A. Baba, R. Nomura, H. Matsuda
Tetrahedron Lett. 1995, 36(52), 9497-9500.
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