ANIONS LITHIENS DERIVES D'AZA-2 ALLYLPHOSPHONATES. SYNTHESE REGIO ET STEREOSPECIFIQUE DE NOUVELLES δ1-PYRROLINES

DOI: 10.1016/S0040-4039(00)74564-3

Source and publish data:

Tetrahedron Letters p. 1315 - 1318 (1980)

Update date:2022-09-26

Topics:

Authors:

Dehnel, Andre

Lavielle, Gilbert

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

Article abstract of DOI:10.1016/S0040-4039(00)74564-3

Novel δ¹-pyrrolins are obtained by the 1,3-cycloaddition of lithio-anions derived from 2-aza-allylphosphonates on actived double bonds; phosphite is then eliminated.

Full text of DOI:10.1016/S0040-4039(00)74564-3

Products guided by the article

Product name:1-Methyl-3-phenyl-2-aza-spiro[4.5]dec-1-ene-4-carboxylic acid ethyl ester

Cas No:343235-90-5

R&D Labs maybe for 343235-90-5

ZHEJIANG SYNOSE TECH CO.,LTD.

website:https://www.synose.com/

Contact:86-579-82275537

Address:No.1958 Liyu Road , jinhua,zhejiang,China
Shanghai Sinofluoro Scientific Co., Ltd

Contact:+86-21-64279360

Address:Room 1006,Building 3,#58 East Xinjian Road, Shanghai ,201100,China,
Suzhou Jingye Medicine & Chemical Co., Ltd

Contact:+86-512-66658588

Address:No. 88, Sanlian Street, Jinfeng Road, Suzhou New District, Jiangsu Province, P. R. China
Hunan Dinuo Pharmaceutical Co.,Ltd.

Contact:86-731-88280100*8561

Address:Bio-pharmaceutical industrial park, Liuyang, Hunan, China
Shanghai Taibao Pharmaceutical Technology Co., Ltd(expird)

Contact:021-52217366

Address:shanghai

Relevant to this article

Doi:10.1039/j39710001332
(1971)
An Air-Stable Nickel(0) Phosphite Precatalyst for Primary Alkylamine C-N Cross-Coupling Reactions

Doi:10.1002/ejoc.201500734
(2015)
Stereoselective Synthesis of Octahydro-3-oxospiropyran> Systems

Doi:10.1021/jo00207a039
(1985)
Studies of tertiary amine oxides. LXV. Reaction of quinoline 1-oxide with tosyl chloride in the presence of triethylamine

Doi:10.1248/cpb.28.424
(1980)
A novel and simple method for the preparation of (R)- and (S)-pyrrolidine-2-phosphonic acids: Phosphonic acid analogues of proline

Doi:10.1016/j.tetasy.2013.10.013
(2013)
Doi:10.1021/jo01125a018
(1955)

Article Doi