A FACILE, STEREOCONTROLLED ENTRY TO KEY INTERMEDIATES FOR THIENAMYCIN SYNTHESIS FROM ETHYL (S)-3-HYDROXYBUTANOATE

DOI: 10.1246/cl.1985.1343

Source and publish data:

Chemistry Letters p. 1343 - 1346 (1985)

Update date:2022-07-30

Topics:

Authors:

Chiba, Toshiyuki

Nagatsuma, Masako

Nakai, Takeshi

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

Article abstract of DOI:10.1246/cl.1985.1343

A new synthetic approach to optically active key intermediates for thienamycin synthesis is described which involves the highly stereocontrolled transformation of the 2-azetidinone obtained via the condensation of ethyl (S)-3-hydroxybutanoate with the N-s

Full text of DOI:10.1246/cl.1985.1343

Products guided by the article

Product name:Benzoic acid (R)-1-((3S,4R)-2-oxo-4-trimethylsilanylethynyl-azetidin-3-yl)-ethyl ester

Cas No:101067-90-7

R&D Labs maybe for 101067-90-7

SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai
Guangxi Bonger Pharmaceutical Co., Ltd

website:http://napo.lookchem.com/

Contact:+86-18817331185

Address:Donghai Industrial Zone, Tiandong Country,Guangxi,China
Goldwills Pharmaceuticals Co., Ltd.

Contact:0916-2237889 13991621155

Address:North Suburb of Hanzhong city, Shaanxi Province
Shanghai Pengkai Chemical Co.,Ltd

Contact:+86-21-60526671

Address:No.4226 Duzhuang Rd Minhang District Shanghai China
Xinjiang Zhongtai Chemical Co., Ltd.

Contact:+86-991-8788172

Address:NO.78 XISHAN RD.URUMQI，CHINA

Relevant to this article

Triazole-linked dumbbell oligodeoxynucleotides with NF-κB binding ability as potential decoy molecules

Doi:10.1021/jo702459b
(2008)
Synthesis of 3-substituted 4H-1-benzothiopyran-4-ones

Doi:10.1002/jhet.5570220342
(1985)
Stereoisomeric effect on antimicrobial activity of a series of quaternary ammonium salts

Doi:10.1016/S0014-827X(97)00003-7
(1998)
Doi:10.1016/S0040-4039(01)82770-2
(1966)
Chitosan–silica sulfate nanohybrid: a highly efficient and green heterogeneous nanocatalyst for the regioselective synthesis of N-alkyl purine, pyrimidine and related N-heterocycles via presilylated method

Doi:10.1007/s11696-019-00863-1
(2020)
6-(3,4-dichlorophenyl)-1-[(methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: A new potent and selective triple reuptake inhibitor

Doi:10.1021/jm100481d
(2010)

Article Doi