Total synthesis of calyculin A-Construction of the C(9)-C(37) fragment

DOI: 10.1039/CC9960000871

Source and publish data:

Chemical Communications p. 871 - 872 (1996)

Update date:2022-07-29

Topics:

Authors:

Yokokawa, Fumiaki

Hamada, Yasumasa

Shioiri, Takayuki

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

Article abstract of DOI:10.1039/CC9960000871

The potent protein phosphatase inhibitor calyculin A is formally synthesized via construction of the C(9)-C(37) fragment 2 by a Wittig reaction of the C(9)-C(25) spiroketal fragment with the C(26)-C(37) phosphonium salt.

Full text of DOI:10.1039/CC9960000871

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:2-((S)-3-{[(4S,5S)-5-((S)-1-Benzyloxycarbonylamino-2-methoxy-ethyl)-2,2-dimethyl-[1,3]dioxolane-4-carbonyl]-amino}-1-methyl-propyl)-oxazole-4-carboxylic acid methyl ester

Cas No:177212-28-1

R&D Labs maybe for 177212-28-1

shandong lukang animal & plant drug trading co.,ltd.

Contact:15853765968

Address:floor 9, lukang ,jingying building,#173,taibai building west road,jining city,shandong,china
Watson International Ltd

Contact:+44 (0)2036089360-31

Address:Chanceryhouse,Chancery Lan
Chemsigma International Co.,Ltd.

website:http://www.chemsigma.com

Contact:86-025-58748998

Address:Rm.705, 15th Building,Rd.Xinke II
jiangsu hualin chemical co.,ltd.

Contact:86-25-87787402

Address:jaingsu,china
Changzhou Ansciep Chemical Co.,Ltd.

Contact:+86 519 8630 5871

Address:A-710 Boan International, 8 East Guangdian Road,Wujin,Changzhou

Relevant to this article

Cyclobutadiene cobalt complexes as catalysts for insertion of diazo compounds into X–H bonds

Doi:10.1016/j.mencom.2021.04.022
(2021)
New heterocyclic system based on vinylsulfonylfluorobenzene and X-ray structural study of this compound

Doi:10.1007/BF01433984
(1996)
Facile synthesis and biological evaluation of assorted indolyl-3-amides and esters from a single, stable carbonyl nitrile intermediate

Doi:10.1016/j.tetlet.2015.02.090
(2015)
Cyclization of a chiral oxazolidine as a key-step for the synthesis of functionalized piperidines

Doi:10.1016/0040-4039(96)00767-8
(1996)
Ultrasound promoted efficient and green synthesis of β-amino carbonyl compounds in aqueous hydrotropic medium

Doi:10.1016/j.ultsonch.2011.12.001
(2012)
5-aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines as potent, orally active, nonsteroidal progesterone receptor agonists: The effect of D-ring substituents

Doi:10.1021/jm9705770
(1998)

Article Doi