Studies on pyrrolidinones. Synthesis of 2-(5-oxo-2-pyrrolidinyl)-1,3,4- oxadiazoles and 2-(5-oxo-2-pyrrolidinyl)benzimidazoles

DOI: 10.1002/jhet.5570300414

Source and publish data:

Journal of Heterocyclic Chemistry p. 921 - 927 (1993)

Update date:2022-07-29

Topics:

Authors:

Cauliez Cauliez

Couturier

Rigo Rigo

Fasseur Fasseur

Halama Halama

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

Article abstract of DOI:10.1002/jhet.5570300414

Full text of DOI:10.1002/jhet.5570300414

Products guided by the article

Product name:2-Pyrrolidinone, 5-(5-methyl-1,3,4-oxadiazol-2-yl)-1-(phenylmethyl)-

Cas No:105985-11-3

R&D Labs maybe for 105985-11-3

Changsha Huajing Powdery Material Technological Co., Ltd.

Contact:86-731-88879686

Address:Building 2, West Garden, Main Campus of Central South University, Changsha, Hunan Province, China
LinHai Cina Chemical Co., LTD.

Contact:0576-85580989

Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
Wuhan HengHeDa Pharm Co., Ltd

Contact:86-27-84888681

Address:Wuhan economic & technology development zone
SPE Chemicals Co.,Ltd

Contact:

Address:ROOM 1715, No#345 Jin Xiang Road, Pudong District
Shandong Xiangde Biotechnology Co., Ltd

Contact:+86 -15066639877

Address:Sanba street

Relevant to this article

P-Chiral Thioxaphosphoranesulphenyl Chlorides 1P(S)SCl>. Unique Stereochemical Probe for the Nucleophilic Displacements at the Dico-ordinate Sulphur

Doi:10.1039/c39890001694
(1989)
Metal substituted diazo esters as substrates for cross coupling reactions

Doi:10.1016/S0040-4020(96)01194-5
(1997)
Synthesis and thermally stable helix-dimer formation of amidohelicene oligomers

Doi:10.1246/bcsj.20100041
(2010)
A COMPARISON OF ACID LABILE LINKAGE AGENTS FOR THE SYNTHESIS OF PEPTIDE C-TERMINAL AMIDES

Doi:10.1016/S0040-4039(01)80764-4
(1989)
Gold-catalyzed formation of aryl-fused pyrazolooxazepines via intramolecular regioselective 7-exo-dig cyclization

Doi:10.1039/C8OB03157F
(2019)
Indanol-Based Chiral Organoiodine Catalysts for Enantioselective Hydrative Dearomatization

Doi:10.1002/anie.201803889
(2018)

Article Doi