Synthesis of 3-aminonocardicinic acid, the basic nucleus of nocardicins

DOI: 10.1246/bcsj.55.1234

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1234 - 1237 (1982)

Update date:2022-08-04

Topics:

Authors:

Hatanaka

Noguchi Noguchi

Ishimaru

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

Article abstract of DOI:10.1246/bcsj.55.1234

Full text of DOI:10.1246/bcsj.55.1234

Products guided by the article

Product name:(R)-(4-Benzyloxy-phenyl)-[(S)-2-oxo-3-(2,2,2-trichloro-ethoxycarbonylamino)-azetidin-1-yl]-acetic acid benzhydryl ester

Cas No:82304-93-6

R&D Labs maybe for 82304-93-6

Hebei Tianxiang Biological & Pharmaceutical Co., Ltd

Contact:86-0312-6615158

Address:No 42 fazhan street qingyuan county
hangzhou sunchem trading co., ltd.

Contact:13588470430--

Address:Room 406-407, the 4th Building, No549
Yingkou Sanzheng New Technology Chemical Industry Co., Ltd.

Contact:+86-417-2927806

Address:yingkou
Kaymossy BioChem Tech Co., Ltd

website:http://www.kaimosi.com

Contact:0571-87191913/0571-87199097

Address:Room 215, Building 3rd, No.288 Ningxia Road, Qingdao city, China
Wuhan Shengmao Corp

website:http://www.shengmaochem.com

Contact:86-27-82853423, 82819281

Address:Rm 202, A Unit Huaqiao Building No. 2, Lihuangpi Road, Wuhan, China

Relevant to this article

Strigolactone analogues derived from dihydroflavonoids as potent seed germinators for the broomrapes

Doi:10.1021/acs.jafc.9b08044
(2020)
Catalytic oxidative carbonylation of primary and secondary diamines to cyclic ureas. Optimization and substituent studies

Doi:10.1021/jo0109319
(2002)
A 4′-C-ethynyl-2′,3′-dideoxynucleoside analogue highlights the role of the 3′-OH in anti-HIV active 4′-C-ethynyl- 2′-deoxy nucleosides

Doi:10.1021/jm049550o
(2004)
Chemical modification of maltose. IV. Synthesis of 4-O-α-D-altropyranosyl-D-glucopyranose

Doi:10.1248/cpb.29.421
(1981)
Stable monocyclic monoalkoxyhalophosphoranes: Possible examples of structures on the borderline between haloalkoxyphosphoranes and alkoxyphosphonium halides

Doi:10.1021/ja00400a037
(1981)
Doi:10.1021/ja01518a048
(1959)

Article Doi