Synthesis of a C1-C14 subunit of the macrodiolide antibiotics pamamycin-607 and pamamycin-635B

DOI: 10.1016/0040-4039(95)00471-N

Source and publish data:

Tetrahedron Letters p. 3091 - 3094 (1995)

Update date:2022-08-04

Topics:

Authors:

Walkup Walkup

Kim Kim

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

Article abstract of DOI:10.1016/0040-4039(95)00471-N

A nonracemic C₁-C₁₄ portion of the antibiotics pamamycin-607 and -635B was prepared using a route which features two stereoselective aldol reactions (including an apparent kinetic resolution via the Evans aldol reaction), a stereospe

Full text of DOI:10.1016/0040-4039(95)00471-N

Products guided by the article

Product name:(2S,3R,4S)-4-{(2S,5R)-5-[(R)-1-(2,6-Di-tert-butyl-4-methoxy-phenoxycarbonyl)-ethyl]-tetrahydro-furan-2-yl}-3-hydroxy-2-methyl-pentanoic acid methyl ester

Cas No:164413-26-7

R&D Labs maybe for 164413-26-7

Guangzhou Chemical Reagent Factory

Contact:+86-20-8435 9820 or 8435 7345

Address:Southern Guangzhou, Guangdong, China
Beijing Apis Biotechnology Co., Ltd.

Contact:86-010-67856775-8551

Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Changzhou Ansciep Chemical Co.,Ltd.

Contact:+86 519 8630 5871

Address:A-710 Boan International, 8 East Guangdian Road,Wujin,Changzhou
Kunming Biohome Technology Co. Ltd.

website:http://www.biohometech.com/

Contact:86-871-67428869

Address:kunming
Jingzhou TianHe Sci&Tech Chemical Co., Ltd.

Contact:86-716-8331612

Address:Jiangjin Road, #18, High-grade technology industries development district, Jingzhou city, Hubei province

Relevant to this article

Intramolecular catalytic Friedel-Crafts reactions with allenyl cations for the synthesis of quinolines and their analogues

Doi:10.1021/ol049301u
(2004)
An efficient synthesis of 3-substituted isoquinoline and pyridine derivatives by gold catalyzed intramolecular cyclization from o-alkynyloximes

Doi:10.1002/jhet.2109
(2014)
Doi:10.1039/C19670000399
(1967)
Heterocyclization of derivatives of 4-oxoalkanoic acids to 1,5-disubstituted pyrrolin-2-ones

Doi:10.1023/A:1011957011038
(2001)
Doi:10.1016/S0040-4039(00)75394-9
(1968)
Facial Selectivity in Cycloadditions of a Chiral Ketene Acetal under Microwave Irradiation in Solvent-Free Conditions. Configurational Assignment of the Cycloadducts by NOESY Experiments and Molecular Mechanics Calculations

Doi:10.1021/jo00118a037
(1995)

Article Doi