A total synthesis of (±)-tirandamycin B

DOI: 10.1021/ja00023a029

Source and publish data:

Journal of the American Chemical Society p. 8791 - 9796 (1991)

Update date:2022-08-05

Topics:

Authors:

Shimshock

Waltermire

DeShong DeShong

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

Article abstract of DOI:10.1021/ja00023a029

Full text of DOI:10.1021/ja00023a029

Products guided by the article

Product name:(1R,3S,4S,5R)-3-((S)-2-Benzyloxy-1-methyl-ethyl)-1,4-dimethyl-8-triisopropylsilanyloxymethyl-2,9-dioxa-bicyclo[3.3.1]non-7-en-6-one

Cas No:137628-54-7

R&D Labs maybe for 137628-54-7

Linyi VIHO Chemical Co.,Ltd

Contact:86-15588110016

Address:LINYI CITY,SHANDONG PROVINCE,CHINA
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone
FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com
Yingkou Sanzheng Organic Chemical Co. Ltd.

Contact:+86-417-3638818

Address:25 Gengxinli Village, Daqing Road, Yingkou, Liaoning, China
Luojiang Chenming Biological Products Co

Contact:+86 15000297032

Address:GROUP NO.4, HE SHENG VILLAGE, PANLONG TOWN,

Relevant to this article

Total synthesis of herbimycin A

Doi:10.1016/S0040-4039(00)79452-4
(1991)
Flavone C-glycosides from the flowers of Trollius chinensis and their anti-complementary activity

Doi:10.1080/10286020.2012.760545
(2013)
Unequivocal experimental evidence for a unified lithium salt-free wittig reaction mechanism for all phosphonium ylide types: Reactions with β-heteroatom-substituted aldehydes are consistently selective for cis-oxaphosphetane-derived products

Doi:10.1021/ja300943z
(2012)
Synthesis and study of the antiradical and antioxidant activity of foridon analogs

Doi:10.1007/BF02524407
(2000)
Enantioselective β-vinylation of α,β-unsaturated aldehydes using a β-nitroethyl sulfone as vinyl anion equivalent

Doi:10.1002/ejoc.201200150
(2012)
Base-Mediated Generation of Ketenimines from Ynamides: [3+2] Annulation with Azaallyl Anions

Doi:10.1002/adsc.202100047
(2021)

Article Doi