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

Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi
Tianjin Bright Future Technology Co., Ltd

Contact:0086-22-58016666

Address:NO.136 DongTeng Lake Street Tianjin Economic and Technology Development Area,Tainjin,China
SHENYANG COMEBOARD TECHNOLOGY CO., LTD

Contact:+86-24-25724626

Address:Room2210,Tianbao International Building,No.8-1 Weigong South Street,Tiexi District,Shenyang,China
Shanghai Cheerchem Co., Ltd.

Contact:86-21-50966856

Address:Building 5,300 Chuanzhan Road,Pudong New District,Shanghai
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,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