SYNTHESIS OF MACROLIDE ANTIBIOTIC. 20. SYNTHESIS OF ERYTHRONOLIDE A

DOI: 10.1007/BF00963026

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 179 - 183 (1990)

Update date:2022-08-05

Topics:

Authors:

Sviridov, A. F.

Ermolenko, M. S.

Yashunskii, D. V.

Borodkin, V. S.

Kochetkov, N. K.

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

Article abstract of DOI:10.1007/BF00963026

A complete, stereocontrolled synthesis for erythronolide A was carried out by fusion of the (C⁹-C¹³) + (C⁷-C⁸) + (C%&1-C⁶) fragments from levoglucosan in 61 steps with 0.28percent total yield.

Full text of DOI:10.1007/BF00963026

Products guided by the article

Product name:(2R,3R)-2-[(4R,5S,6R)-6-[(S)-2-((R)-Benzenesulfinyl)-1-methyl-ethyl]-2-(4-methoxy-phenyl)-5-methyl-[1,3]dioxan-4-yl]-pentane-2,3-diol

Cas No:129269-52-9

R&D Labs maybe for 129269-52-9

Shanghai Science Peptide Biological Technology Co.,ltd

website:http://www.scipeptide.com

Contact:+86-21-51099675

Address:No.8 Changyang Rd
Jiangsu Institute of Ecomones Co., Ltd

website:http://www.jsmone.com

Contact:+86-519-82821700

Address:95 Huanyuan N. Road, Jintan, Jiangsu, China
Shanghai birch chemical technology co.,ltd

Contact:+86-21-54096810

Address:No.2588,Jungong Road,Shanghai,China
Xi'an Terra Biochem Co. Ltd.

Contact:0086-29-88315623

Address:S711, Innovation Bldg No.25 Gaoxin 1st Rd, Xian P.R of China 710075
Shanghai Dianyang Industry Co.,ltd

Contact:+86 21 6492 4669

Address:Chejing RD, Songjiang District, Shanghai, China

Relevant to this article

Doi:10.1039/jr9640003931
(1964)
LACTAM AND ACID AMIDE ACETALS. 71. NEW SYNTHESIS OF 3-NITRO-6-HYDROXYINDOLE DERIVATIVES

Doi:10.1007/BF00529475
(1992)
Reaction of β-Nitroenamines with Electrophilic Reagents. Synthesis of β-Substituted β-Nitroenamines and 2-Imino-5-nitro-4-thiazolines

Doi:10.1021/jo00209a042
(1985)
Stereoselective synthesis of isoxazolidines through Pd-catalyzed carboetherification of N-butenylhydroxylamines

Doi:10.1002/anie.200701386
(2007)
ADDITION REGIOSELECTIVE D'ENOLATES DE CETONES AUX α-ENONES INFLUENCE DES FACTEURS STERIQUES SUR L'ORIENTATION ET LA REVERSIBILITE DES REACTIONS

Doi:10.1016/0040-4020(84)85094-2
(1984)
Preparation and ¹H NMR study of anomeric 6-deoxyhexopyranosyl azides

Doi:10.1002/jlac.198519850112
(1985)

Article Doi