2007

Coupling Reaction of Alkyl Chlorides with Silyl Enolates Catalyzed by Indium Trihalide
Yoshihiro Nishimoto, Makoto Yasuda, and Akio Baba
Org. Lett., ASAP Article

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(22) , 8588-8590.

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 (Advance Article)

Germanium(II)-Mediated Reductive Cross-Aldol Reaction of Aldehydes: Synthesis of Aldols withDiastereocontrolled Quaternary Carbon Centers
S.-y. Tanaka, M. Yasuda, A. Baba
Synlett 2007, 1720-1724.

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.

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.

2006
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.

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.

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.

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.

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.

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.

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.

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.

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.

2005
In-or In(I)-Employed Tailoring of the Stereogenic Centers in the Reformatsky-Type Reactions ofSimple Ketones, a-Alkoxy Ketones and b-Keto Esters
Babu, S. A.; Yasuda, M.; Shibata, I.; Baba A.
J. Org. Chem. 2005, 70, 10408-10419.

Dihaloindium Hydride as Novel Reducing Agents
Baba, A.; Shibata I.
The Chemical Record, 2005, 5, 323-335.

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.

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.

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.

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.

2004
Triethylsilane-Indium(III) Chloride System as a Radical Reagent
Naoki Hayashi, Ikuya Shibata, and Akio Baba*
Org. Lett. 2004, 6(26) 4981-4983.

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.

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

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.

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

Allylic Tantalums as Highly Imine-selective Reagents
Ikuya Shibata, Kyo Nose, Makoto Yasuda and Akio Baba
J. Org. Chem., 2004, 69, 2185-2187

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

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.

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 (1) 137-139

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
(1)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.

(2)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.

(3) 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.

(4) 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.

(5) 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.

(6) 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.

(7) 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.

(8) 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.

(9) Ionic Activation of Tin Hydrides
Ikuya Shibata and Akio Baba
Curr. Org. Chem. 2002, 6 , (8) 665-693.

(10) 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
(1) 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.

(2) 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.

(3) 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.

(4) 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.

(5) 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.

(6) A Highly syn-Selective Allylation of Aldehydes in Water;
Ikuya Shibata, NaritoshiYoshimura, Masahiro Yabu, Akio Baba;
Eur. J. Org. Chem., 2001, 3207-3211.

(7) Indium(III) Chloride-Catalyzed Coupling Reaction of Acid Chlorides and Allylic Tins;
Katsuyuki Inoue, Yasuhiro Shimizu, Ikuya Shibata, Akio Baba;
Synlett 2001, 1659-1661.

(8) Synthetic Application of a Series of Organotin Hydride;
Ikuya Shibata, Akio Baba;
Main Group Metal Chemistry, 2001, 24, 637-646.

(9) 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.

2000

(1) 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.

(2) Reductive Amination Promoted by Tributyltin Hydride

T. Suwa, E. Sugiyama, I. Shibata, A. Baba

Synlett 2000, 556-558.

(3) 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.

(4) 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.

(5) Chemoselective Reductive Amination of Aldehydes and Ketones by Dibutylchlorotin Hydride-HMPA Complex

T. Suwa, E. Sugiyama, I. Shibata, A. Baba

Synthesis 2000, 789-800.

(6) 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.

(7) 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.

(8) 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

(1) 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.

(2) 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.

(3) 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.

(4) 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.

(5) Highly Diastereoselective Aldol Synthesis from a-Iodo Ketones in Aqueous Media

I. Shibata, M. Kawasaki, M. Yasuda, A. Baba

Chem. Lett. 1999, 689-690.

(6) 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.

(7) 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.

(8) Synthetic Applications of Coordinated TIN Enolates and TIN Hydrides

A. Baba, I. Shibata, M. Yasuda

Phosphorus, Sulfur and Silicon, 1999, 150-151, 293-298.

1998

(1) Halogen Substituted Tin Hydride System for Chemo-, Regio-, and Stereocontrolled Reductions

I. Shibata, A. Baba

Reviews on Heteroatom Chemistry 1998, 18, 247-275.

(2) 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.

(3) 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.

(4) 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.

(5) 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.

(6) 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.

(7) 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.

(8) 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.

(9) 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.

(10) Indium Trichloride Catalyzed Reductive Friedel-Crafts Alkylation of Aromatics Using Carbonyl Compounds

T. Miyai, Y. Onishi, A. Baba

Tetrahedron Lett. 1998, 39, 6291-6294.

(11) 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.

(12) Dibutyltin Chloride Hydride Complex as a Novel Reductant for Chemoselective Redutive Amination

I. Shibata, T. Suwa, E. Sugiyama, A. Baba

Synlett 1998, 1081-1082.

1997

(1) Selective Reactions of Organotin(IV) Enolates Using High-Coordination Method

Makoto Yasuda, Ikuya Shibata, Akio Baba, Haruo Matsuda

Recent Research Developments in Pure & Applied Chemistry1997, 1, 55-71.

(2) 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.

(3) 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.

(4) Indium Triiodide(InI3)-Catalyzed Allylation of Carbonyl Compounds by Allylic Tins

T. Miyai, K. Inoue, M. Yasuda, A. Baba

Synlett 1997, 6, 699-700.

(5) 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.

1996,

(1) 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.

(2) 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.

(3) 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.

1995

(1) 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.

(2) 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.

(3) 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.

(4) 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.

(5) 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.