I. Shibata

发表

Improvement of extractive alkylation gas chromatography of short-chain carboxylic acids in aqueous solution.

S. Tsunoi, Shigemi Ueda, Noriyuki Takemoto, 2021, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

Catalytic Annulation of Epoxides with Heterocumulenes by the Indium-Tin System

A. Baba, Itaru Suzuki, I. Shibata, 2018, Molecules.

Highly efficient synthesis of cyclic carbonates from epoxides catalyzed by indium tribromide system

A. Baba, I. Shibata, Akira Imakuni, 2011 .

NMR Studies of Five-Coordinate Tin Enolate: An Efficient Reagent for Halo Selective Reaction toward .alpha.-Halo Ketone or .alpha.-Halo Imine

M. Yasuda, A. Baba, N. Sonoda, 1994 .

Indium hydride: a novel radical initiator in the reduction of organic halides with tributyltin hydride

A. Baba, A. Sawada, I. Shibata, 2001 .

Organotin(IV) enamines as selective reagents: Coupling with α-halocarbonyls for synthesis of substituted pyrroles

M. Yasuda, A. Baba, I. Shibata, 1997 .

Triethylsilane-indium(III) chloride system as a radical reagent.

A. Baba, N. Hayashi, I. Shibata, 2004, Organic letters.

Catalytic generation of indium hydride in a highly diastereoselective reductive aldol reaction.

M. Yasuda, A. Baba, I. Shibata, 2004, Angewandte Chemie.

Selective reduction of acid chloride with a catalytic amount of an indium compound

M. Yasuda, A. Baba, I. Shibata, 2000 .

Preparation of a novel indium hydride and application to practical organic synthesis

M. Yasuda, A. Baba, I. Shibata, 1998 .

Synthesis of 1,4-Diketones: Unusual Coupling of Tin Enolates with alpha-Chloro Ketones Catalyzed by Zinc Halides.

M. Yasuda, A. Baba, S. Tsuji, 1997, The Journal of organic chemistry.

Generation of organotantalum reagents and conjugate addition to enones.

A. Baba, I. Shibata, Takeyoshi Kano, 2002, Angewandte Chemie.

9.08 – Tin

M. Yasuda, A. Baba, I. Shibata, 2007 .

Solvent-controlled addition of alkynyltins or allylic tins to aldehydes catalyzed by indium trichloride

R. Nomura, M. Yasuda, A. Baba, 1995 .

Indium(III) chloride-sodium borohydride system: a convenient radical reagent for an alternative to tributyltin hydride system.

A. Baba, A. Sawada, I. Shibata, 2002, Journal of the American Chemical Society.

Catalytic Effect of Five-Coordinate Organotin Bromide or Tetraphenylstibonium Bromide on the Chemo- and Stereoselective Addition of Tin Enolate to α-Halo Ketone

M. Yasuda, N. Sonoda, I. Shibata, 1995 .

Facile control of regioselectivity in the reaction of tin enolates with α-halogeno carbonyls by additives

M. Yasuda, A. Baba, I. Shibata, 1993 .

Change of regioselectivity in the reaction of tin enolates and α-bromo ketones; synthesis of 1,4-diketones under non-radical conditions

M. Yasuda, I. Shibata, H. Matsuda, 1990 .

Formation of N-Tributylstannyl Heterocycle from Bis(tributyltin) Oxide and ω-Haloalkyl Isocyanate. One-Pot Convenient Synthesis of 2-Oxazolidinones and Tetrahydro-2H-1,3-oxazin-2-one

Kenji Nakamura, I. Shibata, H. Matsuda, 1989 .

Transition-metal-free coupling reaction of vinylcyclopropanes with aldehydes catalyzed by tin hydride.

S. Tsunoi, I. Shibata, Ryosuke Ieki, 2015, Chemistry.

Synthesis of oxazolidinones initiated by regio- and diastereo-controlled crotylation of alpha-dicarbonyl compounds.

M. Yasuda, A. Baba, R. Kojima, 2010, Organic & biomolecular chemistry.

One-pot synthesis of heterocyclic compounds initiated by chemoselective addition to β-acyl substituted unsaturated aldehydes with nucleophilic tin complexes

M. Yasuda, A. Baba, I. Shibata, 2007 .

Generation of allylic indium by hydroindation of 1,3-dienes and one-pot reaction with carbonyl compounds.

M. Yasuda, A. Baba, N. Hayashi, 2006, Organic letters.

Dihaloindium hydride as a novel reducing agent.

A. Baba, I. Shibata, 2005, Chemical record.

SIMPLE SYNTHETIC METHOD OF ALLYL- AND VINYL-EPOXIDES BY ALLYLATION OF CARBONYL GROUPS WITH ALLYLIC TINS CATALYZED BY PBI2-HMPA

I. Shibata, Shoji Fukuoka, Akemichi Baba, 1998 .

Allylic tin(IV)-tin(II) chloride-acetonitrile as a novel system for allylation of carbonyls or imines

M. Yasuda, A. Baba, A. Yamamoto, 1996 .

Chlorotrimethylsilane-Acetonitrile System as a New Promoter for Carbonyl Allylation by Diallyldibutyltin.

M. Yasuda, A. Baba, N. Sonoda, 1995 .

Indium(III) Chloride-Catalyzed Coupling Reaction of Acid Chlorides and Allylic Tins

A. Baba, I. Shibata, Katsuyuki Inoue, 2001 .

High chelation control of three contiguous stereogenic centers in the Reformatsky reactions of indium enolates with alpha-hydroxy ketones: unexpected stereochemistry of lactone formation.

M. Yasuda, A. Baba, S. A. Babu, 2006, Organic Letters.

Inter- and intramolecular radical couplings of ene-ynes or halo-alkenes promoted by an InCl3/MeONa/Ph2SiH2 system.

A. Baba, N. Hayashi, I. Shibata, 2005, Organic letters.

Preparation of a Novel Indium Hydride and Application to Practical Organic Synthesis.

M. Yasuda, A. Baba, I. Shibata, 1998 .

Selective Reduction of Acid Chloride with a Catalytic Amount of an Indium Compound.

M. Yasuda, A. Baba, I. Shibata, 2000 .

CHEMOSELECTIVE REDUCTIONS OF IMINO GROUPS BY DIBUTYLTIN CHLORIDE HYDRIDE COMPLEX

T. Moriuchi-Kawakami, T. Suwa, I. Shibata, 1998 .

The reductive amination of aldehydes and ketones by catalytic use of dibutylchlorotin hydride complex.

M. Yasuda, A. Baba, Y. Yasaka, 2006, Chemical communications.

Regioselective ring cleavage of oxiranes catalyzed by organotin halide - triphenylphosphine complex

A. Baba, I. Shibata, H. Matsuda, 1986 .

Cycloaddition of 2‐Methyleneaziridines with Isocyanates Catalyzed by Tin Iodide

S. Yasui, Hiroki Takahashi, S. Tsunoi, 2013 .

Allylic tantalums as highly imine-selective reagents.

M. Yasuda, A. Baba, K. Nose, 2004, The Journal of organic chemistry.

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, A. Baba, K. Hayashi, 1998 .

Ionic Activation of Tin Hydrides

A. Baba, I. Shibata, 2002 .

Remarkable dependency of the regioselectivity in the ring opening of α,β-epoxyketones upon tin halide-Lewis base complexes as catalysts

A. Baba, I. Shibata, H. Matsuda, 1992 .

Cycloaddition reaction of heterocumulenes with oxiranes catalyzed by organotin iodide-Lewis base complex

A. Baba, I. Shibata, H. Matsuda, 1986 .

Conjugate hydrostannation of unsaturated esters by iodotin hydride ate complex.

A. Baba, T. Suwa, I. Shibata, 2001, The Journal of organic chemistry.

In- or In(I)-employed tailoring of the stereogenic centers in the reformatsky-type reactions of simple ketones, α-alkoxy ketones, and β-keto esters

M. Yasuda, A. Baba, S. A. Babu, 2005 .

In- or in(I)-employed diastereoselective Reformatsky-type reactions with ketones: 1H NMR investigations on the active species.

M. Yasuda, A. Baba, S. A. Babu, 2004, Organic letters.

Direct use of 1,3-dienes for the allylation of ketones via catalytic hydroindation

Itaru Suzuki, I. Shibata, K. Yagi, 2020, RSC advances.

Synthesis of six-membered heterocycles via the ring cleavage of α-bromo-γ-butyrolactone promoted by organotin alkoxide

A. Baba, I. Shibata, H. Matsuda, 1988 .

Cycloaddition of oxetanes with heterocumulenes catalyzed by organotin iodide‐lewis base complex

A. Baba, I. Shibata, H. Matsuda, 1987 .

Novel use of organotin halide-base complex in organic synthesis. Cycloaddition reaction of oxetane with isocyanates.

A. Baba, M. Fujiwara, I. Shibata, 1985 .

Synthesis of 1,4‐Diketones: Unusual Coupling of Tin Enolates with α‐Chloro Ketones Catalyzed by Zinc Halides.

M. Yasuda, A. Baba, S. Tsuji, 1998 .

Generation of Prenylhafnium and α‐Selective Addition to Imines

A. Baba, S. Tsunoi, I. Shibata, 2009 .

A Highly syn‐Selective Allylation of Aldehydes in Water

A. Baba, I. Shibata, Masahiro Yabu, 2001 .

Highly Coordinated Tin Hydrides: A Novel Synthesis of Tertiary Amines via Hydrostannation of Imines

T. Kawakami, A. Baba, T. Sugimoto, 1995 .

One-pot synthesis of nitrogen heterocycles initiated by regio- and diastereoselective carbon-carbon bond formation of bifunctional carbonyl compounds.

M. Yasuda, A. Baba, I. Shibata, 2004, Journal of the American Chemical Society.

Synthesis of Nitrogen Heterocycles by Intramolecular Michael Type of Amination via Reduction of Imines with Di-n-butyliodotin Hydride (n-Bu2SnIH)

A. Baba, T. Suwa, I. Shibata, 1999 .

Magnesium Halide‐Catalyzed Synthesis of Oxaspiro[2.5]octenes from a Methylenecyclopropane and Acyl Cyanoalkenes

Itaru Suzuki, I. Shibata, Junko Shimazu, 2021 .

Hydroindation of allenes and its application to radical cyclization.

M. Yasuda, A. Baba, N. Hayashi, 2008, Organic & biomolecular chemistry.

Diastereoselective reductive aldol reaction of enones to ketones catalyzed by halogenotin hydride.

M. Yasuda, A. Baba, Hideto Nakajima, 2010, Chemistry.

Transition-Metal-Free Reductive Coupling of 1,3-Butadienes with Aldehydes Catalyzed by Dibutyliodotin Hydride.

Itaru Suzuki, S. Tsunoi, I. Shibata, 2017, Organic letters.

Organotin Enolates in Organic Synthesis. A Review

A. Baba, I. Shibata, 1994 .

Catalytic [3 + 2] Cycloaddition through Ring Cleavage of Simple Cyclopropanes with Isocyanates.

Itaru Suzuki, S. Tsunoi, I. Shibata, 2015, Organic letters.

Highly diastereoselective reformatsky-type reaction promoted by tin iodide ate complex.

A. Baba, T. Suwa, I. Shibata, 2002, Organic letters.

Remarkable Dependence of Diastereoselectivity on Anhydrous or Aqueous Solvent in the Indium Hydride Promoted Reductive Aldol Reaction of α,β-Unsaturated Ketones

A. Baba, I. Shibata, Katsuyuki Inoue, 2002 .

Dibutyltin Chloride Hydride Complex as a Novel Reductant for Chemoselective Reductive Amination

T. Suwa, I. Shibata, Erika Sugiyama, 1998 .

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

A. Baba, T. Suwa, I. Shibata, 2000 .

Reductive Amination Promoted by Tributyltin Hydride

A. Baba, T. Suwa, I. Shibata, 2000 .

Diastereoselective Synthesis of Spiro[2.3]hexanes from Methylenecyclopropane and Cyanoalkenes Catalyzed by a Tin-Ate Complex

Itaru Suzuki, S. Tsunoi, I. Shibata, 2019, European Journal of Organic Chemistry.

Synthesis of carbocycles by enone-selective reduction using organoiodotin hydride

A. Baba, T. Suwa, I. Shibata, 2000 .

Michael Addition of Ketone Enolates to α,β-Unsaturated Esters or Amides in a One-Pot Procedure: Highly Efficient Effect of Lithium Salt Generated in situ on Organotin Enolate

M. Yasuda, A. Baba, I. Shibata, 2005 .

The First Michael Addition of Metal Ketone Enolates to α,β-Unsaturated Esters under Catalytic Conditions: Tin Enolate with a Catalytic Amount of Tetrabutylammonium Bromide

M. Yasuda, A. Baba, I. Shibata, 1999 .

Control of Both Syn and Anti Stereoselectivity in Michael Additions of Organotin Enolates

K. Yasuda, M. Yasuda, A. Baba, 1998 .

Novel Michael addition promoted by tributylstannylcarbamate. Synthesis of diacylcyclopropanes

I. Shibata, H. Matsuda, Y. Mori, 1993 .

Novel method for generation of an organotin enolate by the cleavage of diketene with bis(tributyltin) oxide, and its Michael reactions

A. Baba, I. Shibata, H. Matsuda, 1993 .

Catalytic cycloaddition of 2-hydroxy ketones with 1,1-dicyanoalkenes.

Itaru Suzuki, S. Tsunoi, I. Shibata, 2016, Organic & biomolecular chemistry.

Synthesis of 4‐Hydroxy‐2‐oxazolidinones Catalyzed by Tin Alkoxides

R. Kojima, Hiroki Takahashi, S. Tsunoi, 2011 .

Highly stereoselective addition of tin enolate to α-chloro cyclic ketone derivatives catalyzed by Ph4SbBr

M. Yasuda, N. Sonoda, I. Shibata, 1994 .

Indium-Employed One-Pot Sequential Double Nucleophilic Attack on a Symmetrical Dicarboxaldehyde

M. Yasuda, A. Baba, S. A. Babu, 2004 .

Solvent‐Controlled Addition of Alkynyltins or Allylic Tins to Aldehydes Catalyzed by Indium Trichloride.

R. Nomura, M. Yasuda, A. Baba, 1996 .

Characteristic Reduction of Ketones by Bu3SnH–Bu4NX System

Tomoyuki Yoshida, I. Shibata, H. Matsuda, 1991 .

Indium(III) Chloride—Sodium Borohydride System: A Convenient Radical Reagent for an Alternative to Tributyltin Hydride System.

A. Baba, A. Sawada, I. Shibata, 2002 .

Chemo- and regioselective reductions of functionalized epoxides by Bu3SnH/Bu3SnI-phosphine oxide

T. Kawakami, A. Baba, I. Shibata, 1995 .

Change of Regioselectivity in the Reaction of Tin Enolates and α‐Bromo Ketones: Synthesis of 1,4‐Diketones Under Non‐Radical Conditions.

M. Yasuda, I. Shibata, H. Matsuda, 1991 .

Reduction of α-chlorocarbonyl compounds by the tributyltin hydride–phosphine oxide combined system. Chemoselective reduction of the carbonyl group

Taro Suzuki, I. Shibata, H. Matsuda, 1988 .

Reaction of tributyltin .omega.-haloalkoxides with isocyanates or carbodiimides. A possibility of the addition of a tin-oxygen bond across the carbon:oxygen group of isocyanate

A. Baba, I. Shibata, H. Matsuda, 1985 .

Catalytic Effect of Five‐Coordinate Organotin Bromide or Tetraphenylstibonium Bromide on the Chemo‐ and Stereoselective Addition of Tin Enolate to α‐Halo Ketone.

M. Yasuda, N. Sonoda, I. Shibata, 1995 .

Reaction of Tri-n-butyltin ω-Haloalkoxide (n-Bu3SnO(CH2)nX) with Isothiocyanate

A. Baba, I. Shibata, H. Matsuda, 1986 .

One-Pot Synthesis of Heterocycles Initiated by Chemoselective Reduction of Bifunctional Carbonyl Compounds

M. Yasuda, A. Baba, I. Shibata, 2006 .

Formation of N‐Tributylstannyl Heterocycle from Bis(tributyltin) Oxide and ω‐Haloalkyl Isocyanate. One‐Pot Convenient Synthesis of 2‐Oxazolidinones and Tetrahydro‐2H‐1,3‐oxazin‐2‐one.

Kenji Nakamura, I. Shibata, H. Matsuda, 1989 .

Control of Product in the Reaction of Tributyltin ω-Haloalkoxide (n-Bu3SnO(CH2)nX) with Diphenylketene

A. Baba, I. Shibata, H. Matsuda, 1986 .

Catalytic cycloaddition of 2-methyleneaziridines with 1,1-dicyanoalkenes.

S. Yasui, Hiroki Takahashi, S. Tsunoi, 2014, Organic letters.

Catalytic conversion of lactide to optically pure heterocycles

Hiroki Takahashi, S. Tsunoi, I. Shibata, 2012 .

Synthesis of Oxazolidinones Initiated by Regio‐ and Diastereocontrolled Crotylation of α‐Dicarbonyl Compounds.

M. Yasuda, A. Baba, R. Kojima, 2010 .

Allylic Tin(IV)-Tin(II) Chloride-Acetonitrile as a Novel System for Allylation of Carbonyls or Imines.

M. Yasuda, A. Baba, A. Yamamoto, 2010 .

Simple Synthetic Method of Allyl- and Vinyl-Epoxides by Allylation of Carbonyl Groups with Allylic Tins Catalyzed by PbI2—HMPA.

I. Shibata, Shoji Fukuoka, Akemichi Baba, 1998 .

Lead Iodide−HMPA as a Novel Catalyst for Chemo- and Diastereoselective Carbonyl Allylation of α,β-Epoxy Ketones with Allylic Stannanes

I. Shibata, H. Matsuda, Shoji Fukuoka, 1997 .

Indium hydride catalyzed chemo- and diastereoselective reductive aldol reactions

S. Tsunoi, I. Shibata, Ryosuke Ieki, 2014 .

Dihaloindium Hydrides as Novel Reducing Agents

A. Baba, I. Shibata, 2007 .

A New Halogen-Exchange Reaction between Sn–F and Li–X: Selective 1,2- and 1,4-Reductions of α,β-Unsaturated Ketones and Effects of Halogen Substituents on the Regioselectivity of Organotin Hydrides

A. Baba, T. Moriuchi-Kawakami, T. Suwa, 1999 .

Novel synthesis of syn-α,β-epoxy alcohols by diastereoselective carbonyl reduction of α,β-epoxy ketones

T. Kawakami, T. Kawakami, N. Sonoda, 1994 .

Chemo- and stereoselective carbonyl reduction of .alpha.,.beta.-epoxy ketones by dibutylfluorostannane

T. Kawakami, A. Baba, I. Shibata, 1993 .

One‐Pot Synthesis of Heterocyclic Compounds Initiated by Chemoselective Addition to β‐Acyl Substituted Unsaturated Aldehydes with Nucleophilic Tin Complexes.

M. Yasuda, A. Baba, I. Shibata, 2007 .

NMR Studies of Three Types of Highly Coordinated Organotin Hydrides: Chemo-, Regio-, and Stereoselective Reduction of 2,3-Epoxy Ketones

T. Kawakami, A. Baba, I. Shibata, 1996 .

Preparation of α,β-Unsaturated Methyl Ketones from Diketene Using Bis(tributyltin) Oxide

I. Shibata, H. Matsuda, M. Nishio, 1993 .

A Novel Darzens type reaction promoted by tributylstannylcarbamate

I. Shibata, H. Matsuda, H. Yamasaki, 1992 .

Reduction of Aldehyde with Tributyltin Hydride-HMPA Combined System

Tomoyuki Yoshida, I. Shibata, H. Matsuda, 1989 .

Formation of N-tributylstannyl-2-oxazolidone from (Bu3Sn)2O and 2-chloroethyl isocyanate

I. Shibata, H. Matsuda, Akemichi Baba, 1986 .

Bu2SnIH-promoted proximal bond cleavage of methylenecyclopropanes and successive radical cyclization and/or Pd-catalyzed coupling reaction.

M. Yasuda, A. Baba, N. Hayashi, 2008, Journal of the American Chemical Society.

Regio- and stereoselective hydrostannation of allenes using dibutyliodotin hydride (Bu2SnIH) and successive coupling with aromatic halides.

M. Yasuda, A. Baba, N. Hayashi, 2007, Chemical communications.

Selective alpha-stannylated addition of di-n-butyliodotin hydride Ate complex to simple aliphatic alkynes.

A. Baba, T. Suwa, I. Shibata, 2001, Journal of the American Chemical Society.

Generation of Allylic Indium by Hydroindation of 1,3‐Dienes and One‐Pot Reaction with Carbonyl Compounds.

M. Yasuda, A. Baba, N. Hayashi, 2007 .

Chlorotrimethylsilane‐Acetonitrile System as a New Promoter for Carbonyl Allylation by Diallyldibutyltin.

M. Yasuda, A. Baba, N. Sonoda, 1995 .

Highly Diastereoselective Aldol Synthesis from α-Iodo Ketones in Aqueous Media

M. Yasuda, A. Baba, M. Kawasaki, 1999 .

Synthetic Applications of Coordinated TIN Enolates and TIN Hydrides

M. Yasuda, A. Baba, I. Shibata, 1999 .

Indium(III) Chloride Catalyzed Coupling Reaction of Acid Chlorides and Allylic Tins.

A. Baba, I. Shibata, Katsuyuki Inoue, 2002 .

Syn/anti diastereoselectivity in the reduction of .alpha.-alkoxy ketones by tin hydride reagents

T. Kawakami, Tomoyuki Yoshida, A. Baba, 1992 .

High Chelation Control of Three Contiguous Stereogenic Centers in the Reformatsky Reactions of Indium Enolates with α‐Hydroxy Ketones: Unexpected Stereochemistry of Lactone Formation.

M. Yasuda, A. Baba, S. A. Babu, 2006 .

Regiocontrolled Addition of Carbonyl Compounds with Allylic Indium Generated by Hydroindation of 1,3-Dienes

M. Yasuda, A. Baba, N. Hayashi, 2008 .

Inter‐ and Intramolecular Radical Couplings of Ene‐ynes or Halo‐alkenes Promoted by an InCl3/MeONa/Ph2SiH2 System.

A. Baba, N. Hayashi, I. Shibata, 2005 .

Chemoselective coupling of .alpha.-bromo aldehydes with a tin enolate derived from the ring opening of diketene by bis(tributyltin) oxide

M. Yasuda, A. Baba, I. Shibata, 1994 .

Synthesis of hydroxy lactones by bis(tributyltin) oxide promoted ring expansion of halo lactones

I. Shibata, H. Matsuda, Fumiyuki Matsuo, 1991 .

Chemoselective Reductions of Imino Groups by Dibutyltin Chloride Hydride Complex.

T. Moriuchi-Kawakami, T. Suwa, I. Shibata, 2010 .

Synthesis of a Novel Ate Tin Hydride Complex Bearing a Nucleophilic Iodide Substituent and 1,4-Regioselective Reduction of α,β-Unsaturated Aldehydes

A. Baba, T. Suwa, I. Shibata, 1999 .

Remarkable difference of chemoselectivity in the reduction of α-bromo ketones with dibutyltin dihydride system

Kenji Nakamura, I. Shibata, H. Matsuda, 1990 .

Synthesis of 5-Membered Sulfur Heterocycles via Tin-Catalyzed Annulation of Mercapto Ketones with Activated Alkenes.

Itaru Suzuki, I. Shibata, Yuki Sakamoto, 2019, The Journal of organic chemistry.

Catalytic Annulation of Diethyl Methylenecyclopropane-1,1-dicarboxylate with 1,1-Dicyanoalkenes.

Itaru Suzuki, S. Tsunoi, I. Shibata, 2017, Organic letters.

Double Alkylation of Tin Enolate Derived from Diketene and Bis(tributyltin) Oxide

A. Baba, I. Shibata, H. Matsuda, 1993 .

Reformatsky Type Reaction Promoted by Hexabutyldistannane

A. Baba, Takashi Yamaguchi, I. Shibata, 1993 .

Synthesis of heterocyclic compounds by the organotin alkoxide-promoted cleavage of .gamma.-bromo .beta.-lactones

A. Baba, I. Shibata, H. Matsuda, 1990 .

4-t-Butylbenzylation of carboxylic acid for GC–MS analysis

Itaru Suzuki, S. Tsunoi, I. Shibata, 2020, SN Applied Sciences.

Assay of short-chain carboxylic acids in plasma and urine using gas chromatography after extractive alkylation

N. Takemoto, S. Tsunoi, Risa Onodera, 2023, Analytical Sciences.

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

A. Baba, T. Suwa, I. Shibata, 2000 .

Catalytic cycloaddition of 2-hydroxy ketones with 1,1-dicyanoalkenes.

Itaru Suzuki, S. Tsunoi, I. Shibata, 2016, Organic & biomolecular chemistry.

Annulation of a Methylenecyclopropane with Cyanoalkenes Catalyzed by Lewis Bases.

Itaru Suzuki, I. Shibata, Nozomi Kasahara, 2023, Chemistry.