Biosynthesis of the lincomycins. 1. Studies using stable isotopes on the biosynthesis of the propyl- anbd ethyl-L-hygric acid moieties of lincomycins A and B

DOI: 10.1021/ja00337a038

Source and publish data:

Journal of the American Chemical Society p. 7873 - 7878 (1984)

Update date:2022-09-26

Topics:

Authors:

Brahme Brahme

Gonzalez

Rolls Rolls

et al. et al.

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

Article abstract of DOI:10.1021/ja00337a038

Full text of DOI:10.1021/ja00337a038

Products guided by the article

Product name:methyl 6,8-dideoxy-6-[(4-ethyl-1-methylprolyl)amino]-1-thiooctopyranoside

Cas No:22083-66-5

R&D Labs maybe for 22083-66-5

AURORA CHEMICAL CO., LTD

Contact:86-532-68629711 13780605697

Address:NO 220 YANAN 3 ROAD,(POST ADMINISTRATION BUILDING),QINGDAO,CHINA
Jiangxi Hito Chemical Co., Ltd.

Contact:+86-792-3170318

Address:No. 6, Tianhong Ave., Xinghuo Industry Park, Yongxiu, Jiujiang, Jiangxi, China
Zhejiang kehong chemical co., ltd

Contact:0086-575-85522000

Address:xiner center RD binhai industrial zone shaoxing zhejiang province P.R.China,312073
Jiangxi Lanqi Fine Chemical S&T Co., Ltd.

Contact:+86-21-64891143

Address:XinJiShan Industrial Area, Zhangshu City, JiangXi Province, China
Aqua Chem Industry Co., Ltd

Contact:+86-515-88356562

Address:No.2, West Daqing Road, Yancheng, Jiangsu, China

Relevant to this article

Doi:10.1039/jr9280001583
(1928)
The synthesis of methyl 2-(benzyloxycarbonyl)amino-3- dimethylaminopropenoate. The synthesis of trisubstituted pyrroles, 3-amino- 2H-pyran-2-ones, fused 2H-pyran-2-ones and 4H-pyridin-4-ones

Doi:10.1002/jhet.5570360135
(1999)
Methoxymethylation of alcohols, phenols, and avermectin aglycones using MOM-2-pyridylsulfide

Doi:10.1021/jo9822582
(1999)
Syntheses of two diastereoisomers of panaxytriol, a potent antitumor agent isolated from Panax ginseng

Doi:10.1016/S0040-4020(99)00352-X
(1999)
THE EFFECT OF ENVIRONMENT ON THE REACTIONS OF THIIRANIUM IONS

Doi:10.1016/S0040-4039(00)99828-9
(1984)
Doi:10.1021/ja02173a012
(1915)

Article Doi