Biosynthetic studies on ansatrienin A. formation of the cyclohexanecarboxylic acid moiety

DOI: 10.1021/ja00065a042

Source and publish data:

Journal of the American Chemical Society p. 5254 - 5266 (1993)

Update date:2022-08-05

Topics:

Authors:

Moore Moore

Cho Cho

Casati Casati

Kennedy Kennedy

Reynolds

Mocek Mocek

Beale Beale

Floss Floss

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

Article abstract of DOI:10.1021/ja00065a042

Full text of DOI:10.1021/ja00065a042

Products guided by the article

Product name:methyl 5-hydroxy<5-2H>cyclohex-1-enecarboxylate

Cas No:148874-40-2

R&D Labs maybe for 148874-40-2

YORK CHEMICALS LTD

Contact:+1 (647) 918 5848

Address:2343 BRIMLEY RD., Suite 250
Shanghai Minstar Chemical Co., Ltd

website:http://www.minstargroup.com

Contact:86-21-18019205509

Address:BUILDING 8, NO.1098, CHUANSHA ROAD, SHANGHAI, CHINA
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
WD Silicone Co., Ltd

Contact:+86-27-87204219, +86-27-87215023

Address:2402, HuiGu Space-time Building, 8 Forest Road, East Lake Hi-Tech Development Zone

Relevant to this article

Complete 1H and 13C NMR Assignments for Apramycin, Sisomicin and Some N- and N,O-Polyacetylated Aminoglycosides

Doi:10.1002/mrc.1260300908
(1992)
Directing the regioselectivity of rhodium(I) catalysed cyclisation of 2-alkynyl benzoic acids

Doi:10.1016/j.poly.2013.06.010
(2013)
Synthesis and characterization of 4-substituted 1-(4-halogenophenyl) pyrrolidin-2-ones with azole and azine moieties

Doi:10.3987/COM-13-12703
(2013)
Useful hydroxylamine derivatives for the synthesis of hydroxamic acids

Doi:10.1016/S0040-4039(00)61187-5
(1992)
Dynamic control of dendrimer-fullerene association by axial coordination to the core

Doi:10.1039/c3cc43249a
(2013)
5′-trityl-substituted thymidine derivatives as a novel class of antileishmanial agents: Leishmania infantum EndoG as a potential target

Doi:10.1002/cmdc.201300129
(2013)

Article Doi