Reductive displacement of allylic acetates by hydride transfer via catalytic activation by palladium(0) complexes

DOI: 10.1016/S0040-4039(00)93615-3

Source and publish data:

Tetrahedron Letters p. 27 - 30 (1980)

Update date:2022-08-02

Topics:

Authors:

Hutchins, Robert O.

Learn, Keith

Fulton, Robert P.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)93615-3

Allylic acetates are reduced to alkenes by reductive displacement by hydride reagents via catalytic activation with Pd(0) complexes. In the absence of hydrides, allylic acetates afford conjugated dienes in DMSO solvent.

Full text of DOI:10.1016/S0040-4039(00)93615-3

Products guided by the article

Product name:6-((E)-Buta-1,3-dienyl)-1-methyl-cyclohexene

Cas No:74423-07-7

R&D Labs maybe for 74423-07-7

Sinochem Jiangsu Co.,Ltd.

Contact:86-25-51817806

Address:No. 216, middle longpan road, jincheng tower, floor 21-22, nanjing ,china
Buffett (China) Holding Co.,Ltd

Contact:4006570891

Address:
RongCheng K&S Chemical Co.,Ltd

Contact:0631-7336369

Address:rongcheng ,shandong province china
Jiaozuo Zhongwen Trading Coporation Limited

Contact:--

Address:East Renmin Road
Richest Group Ltd.

Contact:+86 21 5017 5386

Address:No 999,Jiangyue Rd, Minhang Dist ,201114,Shanghai ,China

Relevant to this article

One-pot, three-component synthesis of arylidenesuccinates and related compounds

Doi:10.1016/S0040-4039(97)01294-X
(1997)
Doi:10.1039/c39790000404
(1979)
Stereoselective chloroacetate aldol reactions: Syntheses of acetate aldol equivalents and darzens glycidic esters

Doi:10.1021/ol0490835
(2004)
Synthetic and mechanistic aspects of 4-substituted-3,5-bis(methoxycarbonyl)isoxazoline N-oxides and the corresponding 3,5-bis-(butylcarbamoyl)isoxazoles derived therefrom

Doi:10.1248/cpb.28.479
(1980)
The synthesis of oligonucleotides that contain 2,4-dinitrophenyl reporter groups

Doi:10.1016/0008-6215(92)84170-W
(1991)
Iodine-catalyzed formation of substituted 2-aminobenzothiazole derivatives in PEG₄₀₀

Doi:10.1039/c6ra15971k
(2016)

Article Doi