A NEW SYNTHESIS OF 3-AMINO-2-ALKENOATES

DOI: 10.1016/S0040-4039(00)87168-3

Source and publish data:

Tetrahedron Letters p. 1597 - 1600 (1982)

Update date:2022-09-26

Topics:

Authors:

Hiyama, Tamejiro

Kobayashi, Kazuhiro

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

Article abstract of DOI:10.1016/S0040-4039(00)87168-3

Magnesium enolates of t-butyl (or ethyl) acetate and t-butyl propionate are found to react with nitriles to gives 3-amino-2-alkenoates having Z configuration.

Full text of DOI:10.1016/S0040-4039(00)87168-3

Products guided by the article

Product name:(Z)-3-Amino-2-methyl-3-phenyl-acrylic acid tert-butyl ester

Cas No:82772-13-2

R&D Labs maybe for 82772-13-2

TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)

Contact:22-58516360

Address:tianjin
Triumph International Development Limilted

website:http://www.jiashengchem.cn/

Contact:+86-536-7971999

Address:Yinhai Road,Shouguang
Tianjin SPHINX SCIENTIFIC LAB.

Contact:+86-022-66211289

Address:Tianda high-tech Park. No.80,the 4th Avenue
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park
Tianjin Realet Chemical Technology Co.,Ltd.

website:http://www.realetchem.com

Contact:+86-022-58788819

Address:shuanggang industrial park

Relevant to this article

Charge-Directed Conjugate Addition Reactions in the Preparation of Substituted Methyl Ketones

Doi:10.1021/jo00146a025
(1982)
Highly stereoselective and efficient total synthesis of (+)-laurencin

Doi:10.1021/ol047877d
(2005)
Chalcogenopyranones from disodium chalcogenide additions to 1,4- pentadiyn-3-ones. The role of enol ethers as intermediates

Doi:10.1002/jhet.5570360322
(1999)
OPTICALLY ACTIVE PERFLUORO-2-PROPOXYPROPIONIC ACID

Doi:10.1246/cl.1980.843
(1980)
Highly stereoselective vinylogous pummerer rearrangement

Doi:10.1080/10426500590913366
(2005)
Facile synthesis of α,α′ disubstituted N-hydroxypyrrolidines and N-hydroxypiperidines via double 1,4-addition of hydroxylamine

Doi:10.1016/j.tetlet.2006.03.064
(2006)

Article Doi