Enantioselective synthesis of the C1-C28 portion of the cytotoxic natural product, amphidinolide B1

DOI: 10.1016/S0040-4039(97)10103-4

Source and publish data:

Tetrahedron Letters p. 7909 - 7910 (1997)

Update date:2022-08-03

Topics:

Authors:

Lee, Duck-Hyung

Lee, Suk-Won

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

Article abstract of DOI:10.1016/S0040-4039(97)10103-4

The C1-C28 portion of the cytotoxic natural product, amphidinolide B1 (1a), was synthesized enantioselectively using as key steps Evans chiral oxazolidinone chemistry, Sharpless asymetric epoxidation, and the orthoester Claisen rearrangement. The overall

Full text of DOI:10.1016/S0040-4039(97)10103-4

Products guided by the article

Product name:(4S,5R)-3-((R)-4-Bromo-2-methyl-pent-4-enoyl)-4-methyl-5-phenyl-oxazolidin-2-one

Cas No:199612-89-0

R&D Labs maybe for 199612-89-0

Sino Rarechem Labs Co.Ltd

Contact:+86-0512-62857507

Address:Boji Science Park, No1688C,Taishan road, Suzhou ,China
Shuanghe Bio-Technology Limited(expird)

Contact:+86-571-61710758,18968016640

Address:Jinqiao north road 916# Fuyang
Changzhou Litong Chemical Co., Ltd.

website:http://www.litonchem.com/

Contact:+86-519-86301238

Address:Laoba Rd, Hutang town Changzhou Jiangsu
Jiangsu Dacheng Pharmaceutical and Chemical Co.,Ltd

Contact:+86-0517-87036900

Address:Chuzhou Chemical park, Huai'an, Jiangsu Province
SHANDONG CREDAGRI CHEMICAL CO., LTD.

Contact:+86-531-88872050

Address:ROOM 601A, BUILDING 2, SHUNTAI SQUARE, NO. 2000 SHUNHUA ROAD, HI-TECH DEVELOPMENT ZONE, JINAN, CHINA.

Relevant to this article

A 1,6-ring closure mechanism for (+)-δ-cadinene synthase?

Doi:10.1021/ja211820p
(2012)
Spontaneous dimerization of 2-(4-methylphenylamino)thiophene

Doi:10.1007/BF02253121
(1997)
Nucleophilic phosphanylation of fluoroaromatic compounds with carboxyl, carboxymethyl, and aminomethyl functionalities - An efficient synthetic route to amphiphilic arylphosphanes

Doi:10.1002/(SICI)1099-0682(199801)1998:1<73::AID-EJIC73>3.0.CO;2-M
(1998)
Optically active cantharidin analogues possessing selective inhibitory activity on Ser/Thr protein phosphatase 2B (calcineurin): Implications for the binding mode

Doi:10.1016/j.bmc.2005.05.013
(2005)
Total synthesis of analogs of topostin B, A DNA topoisomerase I inhibitor. Part 3: Improved synthesis of topostin B-1 analogs

Doi:10.1016/S0040-4020(97)10315-5
(1998)
Structurally simplified zaragozic acid (squalestatin): Stereoselective preparation of a 3,4-unsubstituted derivative

Doi:10.1016/S0040-4039(97)10407-5
(1997)

Article Doi