Total Synthesis of Elfamycins: Aurodox and Efrotomycin. 2. Coupling of Key Intermediates and Completion of the Synthesis

DOI: 10.1021/ja00292a039

Source and publish data:

Journal of the American Chemical Society p. 1695 - 1698 (1985)

Update date:2022-08-02

Topics:

Authors:

Dolle, R. E.

Nicolaou, K. C.

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

Article abstract of DOI:10.1021/ja00292a039

The coupling of key intermediates IV-VIII and the completion of the total syntheses of aurodox (1) and efrotomycin (2) are described.

Full text of DOI:10.1021/ja00292a039

Products guided by the article

Product name:efrotomycin

Cas No:56592-32-6

R&D Labs maybe for 56592-32-6

Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Huayi Isotopes Co.

Contact:+ 86 512 52491118

Address:1 Fuyu Road, Haiyu TownChangshu, Jiangsu, China
Hefei TNJ chemical industry co.,ltd

website:https://www.tnjchem.com

Contact:+86-551-65418695

Address:B911 Xincheng Business Center, Qianshan Road, Hefei Anhui China
Hebei Lead Bio-Chemicals Co., Ltd.

website:http://www.ldbiochem.com

Contact:+86-311-87826503

Address:481, Heping West Road, Shijiazhuang,China
GUANGXI GUANGHONG PHARMACEUTICAL CO.,LTD

website:http://www.irondextran-factory.com

Contact:+8618928624811

Address:No.7 Baota Road, Baota Pharmaceutical Industry Park, Long’an, Nanning, China

Relevant to this article

Doi:10.1039/P19790000956
(1979)
Bond Fixation in Annulenes. 9. Equalization of Ring Inversion and Bond Shifting Energetics in 1,2,3,4-tetramethylcyclooctatetraene. Asymmetric Synthesis, Direct Resolution, and Absolute Configuration of the Optically Active Hydrocarbon

Doi:10.1021/ja00535a033
(1980)
Kinetics of Thermal Pyridine Dissociation of Ni(N-arylsalicylideneaminato)2(pyridine)2 in Solid Phase

Doi:10.1246/bcsj.55.104
(1982)
Deoxygenation of sulfoxides, selenoxides, telluroxides, sulfones, selenones and tellurones with Mg-MeOH

Doi:10.1016/j.tet.2006.11.027
(2007)
Synthesis and coronary vasodilating activity of 2 substituted adenosines

Doi:10.1248/cpb.23.759
(1975)
Doi:10.1002/hlca.19750580318
(1975)

Article Doi