ChemInform Abstract: ADDITION OF ORGANOCOPPER DERIVATIVES TO CONJUGATED ENYNES

F. SCOTT; G. CAHIEZ; J. F. NORMANT; J. VILLIERAS

doi:10.1002/chin.197817092

ChemInform Abstract: ADDITION OF ORGANOCOPPER DERIVATIVES TO CONJUGATED ENYNES

Chemischer Informationsdienst ◽

10.1002/chin.197817092 ◽

1978 ◽

Vol 9 (17) ◽

Author(s):

F. SCOTT ◽

G. CAHIEZ ◽

J. F. NORMANT ◽

J. VILLIERAS

Keyword(s):

Conjugated Enynes

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ChemInform Abstract: STUDY OF THE ADDITION OF SATURATED AND BENZYLIC ORGANOMAGNESIUM COMPOUNDS TO SIMPLE AND FUNCTIONALIZED CONJUGATED ENYNES

Chemischer Informationsdienst ◽

10.1002/chin.197809085 ◽

1978 ◽

Vol 9 (9) ◽

Author(s):

J. AUGER ◽

G. COURTOIS ◽

L. MIGINIAC

Keyword(s):

Conjugated Enynes ◽

Organomagnesium Compounds

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Cobalt‐Catalyzed Chemo‐ and Enantioselective Hydrogenation of Conjugated Enynes

Angewandte Chemie ◽

10.1002/ange.202106566 ◽

2021 ◽

Author(s):

Yanhua Hu ◽

Zhenfeng Zhang ◽

Yangang Liu ◽

Wanbin Zhang

Keyword(s):

Enantioselective Hydrogenation ◽

Conjugated Enynes

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Selective Synthesis of Conjugated Enynes from α-Arylalkynols Using LiCl-Acidic Al2O3 under Solvent-Free Conditions.

ChemInform ◽

10.1002/chin.200304057 ◽

2003 ◽

Vol 34 (4) ◽

Author(s):

Ali Pourjavadi ◽

Gholam Bagheri Marandi

Keyword(s):

Solvent Free ◽

Selective Synthesis ◽

Solvent Free Conditions ◽

Conjugated Enynes

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ChemInform Abstract: Stannylmetalation of Conjugated Enynes.

ChemInform ◽

10.1002/chin.199122085 ◽

2010 ◽

Vol 22 (22) ◽

pp. no-no

Author(s):

R. AKSELA ◽

A. C. OEHLSCHLAGER

Keyword(s):

Conjugated Enynes

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ChemInform Abstract: Enhanced Reactivity of Electron-Deficient Enynes in the Palladium-Catalyzed homo-Benzannulation of Conjugated Enynes.

ChemInform ◽

10.1002/chin.200048054 ◽

2000 ◽

Vol 31 (48) ◽

pp. no-no

Author(s):

Shinichi Saito ◽

Yukiyasu Chounan ◽

Tsutomu Nogami ◽

Tomoko Fukushi ◽

Norie Tsuboya ◽

...

Keyword(s):

Conjugated Enynes ◽

Palladium Catalyzed

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Synthesis of conjugated enynes by assembly of three components, ketones, chloromethyl p-tolyl sulfoxide, and acetylenes, with the magnesium carbenoid 1,2-CC insertion as the key reaction

Tetrahedron Letters ◽

10.1016/j.tetlet.2009.11.082 ◽

2010 ◽

Vol 51 (4) ◽

pp. 633-637 ◽

Cited By ~ 6

Author(s):

Hideki Saitoh ◽

Naoyuki Ishida ◽

Tsuyoshi Satoh

Keyword(s):

Conjugated Enynes ◽

Three Components

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SYNTHESIS OF α,α′-DIFUNCTIONAL CONJUGATED ENYNES

Organic Preparations and Procedures International ◽

10.1080/00304948009458551 ◽

1980 ◽

Vol 12 (3-4) ◽

pp. 213-218 ◽

Cited By ~ 7

Author(s):

Jean-Paul Charpentier ◽

Danielle Mesnard ◽

Léone Miginiac

Keyword(s):

Conjugated Enynes

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Preparation of Selanyl-Substituted Conjugated Enynes by Copper-Catalysed Coupling Reaction of (E)-γ-Selanyl Vinylzirconocene with Acetylenic Bromide

Journal of Chemical Research ◽

10.3184/030823403322597405 ◽

2003 ◽

Vol 2003 (9) ◽

pp. 584-585 ◽

Cited By ~ 2

Author(s):

Meihua Xie ◽

Xian Huang

Keyword(s):

Stereoselective Synthesis ◽

Coupling Reaction ◽

Conjugated Enynes

A stereoselective synthesis of conjugated enynes containing allyl selenide unit is reported. Selanyl-substituted conjugated enynes were obtained by the coupling reaction of ( E)-γ-selanyl vinylzirconocene with acetylenic bromide in the presence of CuCl.

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A novel approach towards the preparation of functionalized alkyne derivatives via ArS-mediated AdE reaction of cobaltcarbonyl complexed conjugated enynes

Tetrahedron ◽

10.1016/j.tet.2010.01.060 ◽

2010 ◽

Vol 66 (12) ◽

pp. 2156-2161 ◽

Cited By ~ 2

Author(s):

Vasily V. Tumanov ◽

Georgy V. Zatonsky ◽

William A. Smit

Keyword(s):

Novel Approach ◽

Conjugated Enynes ◽

Alkyne Derivatives

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Selective synthesis of conjugated enynes from α-arylalkynols using LiCl-Acidic Al2O3 under solvent-free conditions

Journal of Chemical Research ◽

10.3184/030823402103172374 ◽

2002 ◽

Vol 2002 (8) ◽

pp. 378-380 ◽

Cited By ~ 1

Author(s):

Ali Pourjavadi ◽

Gholam Bagheri Marandi

Keyword(s):

Solvent Free ◽

Selective Synthesis ◽

Solvent Free Conditions ◽

Conjugated Enynes

α-Arylalkynols were converted into conjugated enynes (in a selective manner under solvent-free conditions) using the LiCl-acidic Al2O3 couple as catalyst and support.

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