The Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Eetones and Acetals in the Presence of Titanium Tetraalkoxide and Titanium Tetrachloride

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.49.779 ◽

1976 ◽

Vol 49 (3) ◽

pp. 779-783 ◽

Author(s):

Koichi Narasaka ◽

Kenso Soai ◽

Yukiko Aikawa ◽

Teruaki Mukaiyama

Keyword(s):

Titanium Tetrachloride ◽

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

The Michael Reaction

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ChemInform Abstract: THE MICHAEL REACTION OF SILYL ENOL ETHERS WITH α,β-UNSATURATED KETONES AND ACETALS IN THE PRESENCE OF TITANIUM TETRAALKOXIDE AND TITANIUM TETRACHLORIDE

Chemischer Informationsdienst ◽

10.1002/chin.197624094 ◽

1976 ◽

Vol 7 (24) ◽

pp. no-no

Author(s):

KOICHI NARASAKA ◽

KENSO SOAI ◽

YUKIKO AIKAWA ◽

TERUAKI MUKAIYAMA

Keyword(s):

Titanium Tetrachloride ◽

Michael Reaction ◽

Enol Ethers ◽

Unsaturated Ketones ◽

Silyl Enol Ethers ◽

The Michael Reaction

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The Michael reaction of silyl enol ethers or ketene silyl acetals with conjugated nitro olefins activated by Lewis acids: new synthesis of 1,4-diketones and .gamma.-oxo esters

Journal of the American Chemical Society ◽

10.1021/ja00319a040 ◽

1984 ◽

Vol 106 (7) ◽

pp. 2149-2156 ◽

Author(s):

Masaaki Miyashita ◽

Tetsuji Yanami ◽

Toshiaki Kumazawa ◽

Akira Yoshikoshi

Keyword(s):

Lewis Acids ◽

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

New Synthesis ◽

Silyl Acetals ◽

The Michael Reaction

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ChemInform Abstract: THE MICHAEL REACTION OF SILYL ENOL ETHERS OR KETENE SILYL ACETALS WITH CONJUGATED NITRO OLEFINS ACTIVATED BY LEWIS ACIDS: NEW SYNTHESIS OF 1,4-DIKETONES AND Γ-OXO ESTERS

Chemischer Informationsdienst ◽

10.1002/chin.198428087 ◽

1984 ◽

Vol 15 (28) ◽

Author(s):

M. MIYASHITA ◽

T. YANAMI ◽

T. KUMAZAWA ◽

A. YOSHIKOSHI

Keyword(s):

Lewis Acids ◽

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

New Synthesis ◽

Silyl Acetals ◽

The Michael Reaction

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The Michael Reaction of Various Quinones with Silyl Enol Ethers. A Facile Method for the Preparation of Benzofuran and Indole Derivatives

Chemistry Letters ◽

10.1246/cl.1987.2169 ◽

1987 ◽

Vol 16 (11) ◽

pp. 2169-2172 ◽

Author(s):

Teruaki Mukaiyama ◽

Yukihiro Sagawa ◽

Shu Kobayashi

Keyword(s):

Michael Reaction ◽

Indole Derivatives ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

The Michael Reaction

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ChemInform Abstract: The Michael Reaction of Various Quinones with Silyl Enol Ethers. A Facile Method for the Preparation of Benzofuran and Indole Derivatives.

10.1002/chin.198819164 ◽

1988 ◽

Vol 19 (19) ◽

Author(s):

T. MUKAIYAMA ◽

Y. SAGAWA ◽

S. KOBAYASHI

Keyword(s):

Michael Reaction ◽

Indole Derivatives ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

The Michael Reaction

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ChemInform Abstract: Indium-Trichloride Catalyzed Michael Reaction of Silyl Enol Ethers with α,β-Unsaturated Carbonyl Compounds under Neat Condition.

10.1002/chin.199841036 ◽

2010 ◽

Vol 29 (41) ◽

pp. no-no

Author(s):

T.-P. LOH ◽

L.-L. WEI

Keyword(s):

Carbonyl Compounds ◽

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers

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ChemInform Abstract: NEW CROSS ALDOL REACTIONS. TITANIUM TETRACHLORIDE-PROMOTED REACTIONS OF SILYL ENOL ETHERS WITH CARBONYL COMPOUNDS CONTAINING A FUNCTIONAL GROUP

Chemischer Informationsdienst ◽

10.1002/chin.197648143 ◽

1976 ◽

Vol 7 (48) ◽

pp. no-no

Author(s):

K. BANNO

Keyword(s):

Carbonyl Compounds ◽

Titanium Tetrachloride ◽

Functional Group ◽

Aldol Reactions ◽

Enol Ethers ◽

Silyl Enol Ethers

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NEW CROSS ALDOL REACTIONS. THE REACTIONS OF SILYL ENOL ETHERS WITH KETO ESTERS PROMOTED BY TITANIUM TETRACHLORIDE

Chemistry Letters ◽

10.1246/cl.1975.741 ◽

1975 ◽

Vol 4 (7) ◽

pp. 741-744 ◽

Author(s):

Kazuo Banno ◽

Teruaki Mukaiyama

Keyword(s):

Titanium Tetrachloride ◽

Aldol Reactions ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

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ChemInform Abstract: Catalytic Asymmetric C-H Activation of Silyl Enol Ethers as an Equivalent of an Asymmetric Michael Reaction.

10.1002/chin.200125032 ◽

2010 ◽

Vol 32 (25) ◽

pp. no-no

Author(s):

Huw M. L. Davies ◽

Pingda Ren

Keyword(s):

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

Catalytic Asymmetric ◽

Asymmetric Michael Reaction

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ChemInform Abstract: The Stereoselective Michael Reaction of α,β-Unsaturated Thioesters with Silyl Enol Ethers Promoted by Combined Use of Antimony(V) Chloride and Tin(II) Triflate.

10.1002/chin.198830160 ◽

1988 ◽

Vol 19 (30) ◽

Author(s):

S. KOBAYASHI ◽

M. TAMURA ◽

T. MUKAIYAMA

Keyword(s):

Michael Reaction ◽

Enol Ethers ◽

Silyl Enol Ethers ◽

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