SELENOCARBOXAMIDES AS NEW REAGENTS FOR STEREOSPECIFIC DEOXYGENATION OF EPOXIDES UNDER MILD CONDITIONS

DOI: 10.1016/S0040-4039(00)89175-3

Source and publish data:

Tetrahedron Letters p. 669 - 672 (1985)

Update date:2022-08-17

Topics:

Authors:

Ogawa, Akiya

Miyake, Jun-ichi

Murai, Shinji

Sonoda, Noboru

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

Article abstract of DOI:10.1016/S0040-4039(00)89175-3

Selenocarboxamides have been found to be efficient reagents for converting epoxides into olefins stereospecifically in high yields under mild conditions.

Full text of DOI:10.1016/S0040-4039(00)89175-3

Products guided by the article

Product name:Phenylethene

Cas No:100-42-5

R&D Labs maybe for 100-42-5

Dongying J&M Chemical Co., Ltd,

Contact:546-8551108

Address:Room 1219, Zisheng Mansion, Zibo Road, Dongying, Shandong, China
Naturalin Bio-Resource Co., Ltd

website:http://www.naturalin.com

Contact:+86-0731-84430651

Address:B1-402, Lu-Valley Enterprise Square.No.27 Wenxuan Road. Lu-Valley Hi-Tech District.
Chemsky（shanghai）International Co.,Ltd.

Contact:0

Address:0
Lanling Hongchuang Flame Retardant Co., Ltd.

Contact:+86-531-68858132

Address:East Huafeichang Road, Cangshan County, Linyi, Shandong, China (Mainland)
NANCHANG QINZHI SCI&TEC.CO.,LTD(expird)

Contact:+86-13687004106

Address:Hero South Road,Hero Zone,Nanchang,Jiangxi,China

Relevant to this article

Synthesis of (-)-epibatidine

Doi:10.1039/c4ra00770k
(2014)
Ligand symmetry significantly affects spin crossover behaviour in isomeric [Fe(pybox)₂]²⁺complexes

Doi:10.1039/d0dt03978k
(2021)
Selective reduction of yeast transfer ribonucleic acid with sodium borohydride.

Doi:10.1016/0022-2836(67)90260-4
(1967)
N,N-bis(2-hydroxybenzyl)-N-(2-pyridylmethyl)amine, H₂BBPA

Doi:10.1107/S0108270195014739
(1996)
The structure of an ultrathin VO_x (x ≈1) film grown epitaxially on TiO₂ (110)

Doi:10.1016/S0039-6028(00)00543-4
(2000)
Gold-nanoparticle-based catalysts for the oxidative esterification of 1,4-butanediol into dimethyl succinate

Doi:10.1002/cssc.201300420
(2013)

Article Doi