Studies on pyrrolidinones. Synthesis of 5-(5-oxo-2-pyrrolidinyl)-1,3,5-oxadiazole-2-thione derivatives

DOI: 10.1002/jhet.5570220209

Source and publish data:

Journal of Heterocyclic Chemistry p. 287 - 288 (1985)

Update date:2022-09-26

Topics:

Authors:

Rigo Rigo

Couturier

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

Article abstract of DOI:10.1002/jhet.5570220209

Full text of DOI:10.1002/jhet.5570220209

Products guided by the article

Product name:N-benzylpyroglutamic acid hydrazide

Cas No:7535-61-7

R&D Labs maybe for 7535-61-7

Xi'an Herbland Tech Inc.

Contact:+86-29-88710656

Address:South Tai bai Road, High Tech Development Zone, Xi'an China
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA
Guangzhou Shiny Co., Ltd.

website:https://www.sinoshiny.com/products

Contact:+86-20-62802632;62802633

Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
Huaihua Baohua Biotechnology Co.,Ltd

website:http://www.baochengchem.com

Contact:86-519-82698291

Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
Shenyang Xingzhenghe Chemical Co., Ltd.

Contact:024-23509232

Address:No. 33, Naner Road, Heping Dist.

Relevant to this article

One-pot synthesis of 1,3-dinitroalkanes under heterogeneous catalysis

Doi:10.1055/s-2004-829160
(2004)
Stereodivergent total asymmetric synthesis of polyhydroxylated pyrrolidines via tandem allylic epoxidation and intramolecular cyclization reactions

Doi:10.1016/j.tetlet.2004.06.048
(2004)
Tert-Butyl Nitrite Promoted Oxidative Intermolecular Sulfonamination of Alkynes to Synthesize Substituted Sulfonyl Pyrroles from the Alkynylamines and Sulfinic Acids

Doi:10.1021/acs.joc.8b00741
(2018)
Copper(II)-Catalyzed Alkene Aminosulfonylation with Sodium Sulfinates for the Synthesis of Sulfonylated Pyrrolidones

Doi:10.1021/acs.orglett.9b00907
(2019)
Reactions of five-membered zirconacyclocumulenes with diisobutylaluminum hydride

Doi:10.1021/om049705q
(2004)
Synthesis and Characterization of a Series of Orthogonally Protected l-Carnosine Derivatives

Doi:10.1007/s10989-018-9680-2
(2018)

Article Doi