A convergent sythetic route to the tunicamycin antibiotics. Synthesis of (+)-tunicamycin V

DOI: 10.1021/ja00058a060

Source and publish data:

Journal of the American Chemical Society p. 2036 - 2038 (1993)

Update date:2022-08-05

Topics:

Authors:

Myers Myers

Gin Gin

Rogers Rogers

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

Article abstract of DOI:10.1021/ja00058a060

Full text of DOI:10.1021/ja00058a060

Products guided by the article

Product name:tert-butyldimethylsilyl 2-azido-4-O-benzoyl-3-O-<(benzyloxy)methyl>-6-bromo-β-D-galactopyranoside

Cas No:147158-38-1

R&D Labs maybe for 147158-38-1

Jiangxi Global Natural Spice Co., Ltd.

website:https://www.jxhqxl.com/

Contact:+86-796-8106598

Address:No.89, Wenshan Road,South Industrial Park, Jishui County,Jiangxi Province
RongCheng K&S Chemical Co.,Ltd

Contact:0631-7336369

Address:rongcheng ,shandong province china
Luoyang Aoda chemical Co.,Ltd.

Contact:+86-379-67518785 67516588

Address:MiaoWan industry district,YanShi City,Henan,China
Valiant Fine Chemicals Co., Ltd.

Contact:+86 535 6101878/6374484

Address:11 Wuzhishan Rd.,YTETDZ,Yantai,264006,Shandong,China
Airsea(Taizhou) Pharmaceutical Limited(expird)

Contact:+86-576-88057622

Address:Dubei, Duqiao, Linhai, Taizhou, Zhejiang, China Zip: 317016

Relevant to this article

Doi:10.1021/jm00315a027
(1967)
Tandem Michael addition and azanorbornane substance-P antagonists

Doi:10.1016/S0040-4020(97)00371-2
(1997)
Stereoselective synthesis of 4,5-dihydroxy-D-erythro- and 4,5-dihydroxy-D-threo-L-norvaline from D-ribonolactone

Doi:10.1016/S0040-4020(01)85821-X
(1993)
Preparation of macrodiolides via a common chiral building block. Total synthesis of (-)-pyrenophorin and (-)-pyrenophorol

Doi:10.1016/0040-4039(93)89027-N
(1993)
PURIFICATION AND PROPERTIES OF 1,2-DEHYDRORETICULINE REDUCTASE FROM PAPAVER SOMNIFERUM SEEDLINGS

Doi:10.1016/0031-9422(92)80020-F
(1992)
New organotin(IV) chlorides derived from N-(2-hydroxyphenyl)aryloxy sulfamates. Synthesis, characterization and DSC investigation

Doi:10.1007/s12039-018-1586-1
(2019)

Article Doi