New skeletal rearrangements of C and D rings of a 13-oxobaccatin III derivative

DOI: 10.1016/S0040-4020(98)00993-4

Source and publish data:

Tetrahedron p. 15833 - 15844 (1998)

Update date:2022-08-02

Topics:

Authors:

Marder-Karsenti, Raphaele

Dubois, Joelle

Chiaroni, Angele

Riche, Claude

Guenard, Daniel

Gueritte, Francoise

Potier, Pierre

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

Article abstract of DOI:10.1016/S0040-4020(98)00993-4

13-Oxobaccatin II (4) was oxidized to 7,13-dioxo D-secobaccatin III (5). This compound, when treated with base or cyanide ion, underwent rearrangements involving the rupture of the C-7,C-8 bond, the migration of the benzoyl and acetyl groups and intramole

Full text of DOI:10.1016/S0040-4020(98)00993-4

Products guided by the article

Product name:Benzoic acid (1S,2S,3R,4S,8S,10R)-10-acetoxy-4-acetoxymethyl-1,4-dihydroxy-8,12,15,15-tetramethyl-7,9,13-trioxo-tricyclo[9.3.1.0^3,8]pentadeca-5,11-dien-2-yl ester

Cas No:220478-92-2

R&D Labs maybe for 220478-92-2

ZHIJIANG ZENVA SINO COMMERCE AND TRADE CO., LTD.

website:http://www.zenvasino.com

Contact:+86-138-72658998

Address:Shibeishan Road,Zhijiang, Hubei, China
zhenjiang runjing high purity chemical co ltd

Contact:+86-511-83361155

Address:No.8.haixi road,international chemical park
Tocopharm Co., Ltd.

Contact:+86-021-6989-5597

Address:No.80 Yichuan Rd., Putuo District,Shanghai,P.R.China
Tianjin Pharmacn Medical Technology Co.,Ltd.

Contact:86-22-60122566ext.866(English),23359620

Address:Green Industrial Base, 6 Haitaifazhan Sixth Rd., Huayuan Industrial Area, Tianjin, 300384, China
SHANGHAI SYSTEAM BIOCHEM CO., LTD

website:http://www.systeambc.com

Contact:86-021-58380978

Address:Building 87，Lane 669， Dong Jing Road Shanghai,P.R.China

Relevant to this article

A short synthesis and biological evaluation of potent and nontoxic antimalarial bridged bicyclic β-sulfonyl-endoperoxides

Doi:10.1021/jm020584a
(2003)
The effect of DMSO on the borohydride reduction of a cyclohexanone: A formal enantioselective synthesis of (+)-epibatidine

Doi:10.1016/S0040-4039(98)02354-5
(1999)
Dimerization of o-hydroxycyclohexadienones related to calicheamicinone: S(N)2 displacement of the 12α-hydroxyl group

Doi:10.1016/S0040-4020(98)01204-6
(1999)
Second-Generation Tryptamine Derivatives Potently Sensitize Colistin Resistant Bacteria to Colistin

Doi:10.1021/acsmedchemlett.9b00135
(2019)
A convenient route to β-amino propionic acid derivatives

Doi:10.1080/00397919908085739
(1999)
Doi:10.1021/ja01102a036
(1953)

Article Doi