A SIMPLE SYNTHESIS OF α,β-UNSATURATED CARBONYL COMPOUNDS BY TRAPPING THE MICHAEL ADDITION-ENOLATE ANION WITH METHANESULFINYL CHLORIDE

Tamotsu Fujisawa; Atsunari Noda; Tatsuo Kawara; Toshio Sato

doi:10.1246/cl.1981.1159

A SIMPLE SYNTHESIS OF α,β-UNSATURATED CARBONYL COMPOUNDS BY TRAPPING THE MICHAEL ADDITION-ENOLATE ANION WITH METHANESULFINYL CHLORIDE

Chemistry Letters ◽

10.1246/cl.1981.1159 ◽

1981 ◽

Vol 10 (8) ◽

pp. 1159-1160 ◽

Cited By ~ 11

Author(s):

Tamotsu Fujisawa ◽

Atsunari Noda ◽

Tatsuo Kawara ◽

Toshio Sato

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Simple Synthesis ◽

Enolate Anion ◽

The Michael Addition

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ChemInform Abstract: A SIMPLE SYNTHESIS OF α,β-UNSATURATED CARBONYL COMPOUNDS BY TRAPPING THE MICHAEL ADDITION ENOLATE ANION WITH METHANESULFINYL CHLORIDE

Chemischer Informationsdienst ◽

10.1002/chin.198205166 ◽

1982 ◽

Vol 13 (5) ◽

Author(s):

T. FUJISAWA ◽

A. NODA ◽

T. KAWARA ◽

T. SATO

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Simple Synthesis ◽

Enolate Anion ◽

The Michael Addition

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ChemInform Abstract: Unusual Diastereofacial Selectivity in the Michael Addition Reactions of Lithiated 2-Aminoacetates and -acetamides to α,β- Unsaturated Carbonyl Compounds.

ChemInform ◽

10.1002/chin.199318073 ◽

2010 ◽

Vol 24 (18) ◽

pp. no-no

Author(s):

S. KANEMASA ◽

M. NOMURA ◽

Y. TAGUCHI

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Addition Reactions ◽

The Michael Addition

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Unusual Diastereofacial Selectivity in the Michael Addition Reactions of Lithiated 2-Aminoacetates and -acetamides to α,β-Unsaturated Carbonyl Compounds

Chemistry Letters ◽

10.1246/cl.1992.1801 ◽

1992 ◽

Vol 21 (9) ◽

pp. 1801-1804 ◽

Cited By ~ 8

Author(s):

Shuji Kanemasa ◽

Masafumi Nomura ◽

Yasuhisa Taguchi

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Addition Reactions ◽

The Michael Addition

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ChemInform Abstract: N,N-Dialkylthioamides in the Michael Addition to Conjugate Carbonyl Compounds: Regioselectivity, Stereochemistry and Mechanism.

ChemInform ◽

10.1002/chin.199342058 ◽

2010 ◽

Vol 24 (42) ◽

pp. no-no

Author(s):

L. VITEVA ◽

T. GOSPODOVA ◽

Y. STEFANOVSKY

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

The Michael Addition

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ChemInform Abstract: Clay (Montmorillonite K10) Catalysis of the Michael Addition of α,β-Unsaturated Carbonyl Compounds to Indoles: The Beneficial Role of Alcohols.

ChemInform ◽

10.1002/chin.199947144 ◽

2010 ◽

Vol 30 (47) ◽

pp. no-no

Author(s):

Jacques H. Poupaert ◽

Jacques Bukuru ◽

Andrea Gozzo

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Montmorillonite K10 ◽

Beneficial Role ◽

The Michael Addition

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Clay (Montmorillonite K10) Catalysis of the Michael Addition of α,β-Unsaturated Carbonyl Compounds to Indoles: The Beneficial Role of Alcohols

Monatshefte für Chemie - Chemical Monthly ◽

10.1007/pl00010274 ◽

1999 ◽

Vol 130 (7) ◽

pp. 929-932 ◽

Cited By ~ 1

Author(s):

Jacques H. Poupaert ◽

Jacques Bukuru ◽

Andrea Gozzo

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Montmorillonite K10 ◽

Beneficial Role ◽

The Michael Addition

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N,N-DIALKYLTHIOAMIDES IN THE MICHAEL ADDITION TO CONJUGATE CARBONYL COMPOUNDS, REGIOSELECTIVITY, STEREOCHEMISTRY AND MECHANISM

Phosphorus Sulfur and Silicon and the Related Elements ◽

10.1080/10426509308032434 ◽

1993 ◽

Vol 78 (1-4) ◽

pp. 189-198 ◽

Cited By ~ 4

Author(s):

Lilia Viteva ◽

Tzveta Gospodova ◽

Yuri Stefanovsky

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

The Michael Addition

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Indium(I) Iodide Promoted Cleavage of Dialkyl Disulfides — Application of the Michael Addition of Thiolate Anions to Conjugate Carbonyl Compounds and Regioselective Ring Opening of Epoxides.

ChemInform ◽

10.1002/chin.200647095 ◽

2006 ◽

Vol 37 (47) ◽

Author(s):

Brindaban C. Ranu ◽

Tanmay Mandal

Keyword(s):

Michael Addition ◽

Carbonyl Compounds ◽

Ring Opening ◽

Ring Opening Of Epoxides ◽

Dialkyl Disulfides ◽

Thiolate Anions ◽

The Michael Addition

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Study of the Michael addition of β-cyclodextrin–thiol complexes to conjugated alkenes in water

Chemical Communications ◽

10.1039/b411736k ◽

2005 ◽

pp. 669-671 ◽

Cited By ~ 52

Author(s):

N. Srilakshmi Krishnaveni ◽

K. Surendra ◽

K. Rama Rao

Keyword(s):

Michael Addition ◽

The Michael Addition

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An ab initio molecular orbital study of the first step of the catalytic mechanism of thymidylate synthase: the Michael addition of sulfur and oxygen nucleophiles

The Journal of Organic Chemistry ◽

10.1021/jo00131a012 ◽

1995 ◽

Vol 60 (26) ◽

pp. 8375-8381 ◽

Cited By ~ 9

Author(s):

Bert E. Thomas ◽

Peter A. Kollman

Keyword(s):

Ab Initio ◽

Molecular Orbital ◽

Thymidylate Synthase ◽

Michael Addition ◽

Catalytic Mechanism ◽

Molecular Orbital Study ◽

Orbital Study ◽

The Michael Addition

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