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

hangzhou verychem science and technology co.ltd

website:http://www.verypharm.com

Contact:+86-571-88162785; 88162786

Address:F1502, 753 Shenhua road, Hangzhou, China
Shanghai KFSL Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-39971718

Address:859 jiadingchengliu shanghai
SNC | GOOD FORTUNE

Contact:0086-22-2822 1962 / 2822 1963

Address:B-808, No. 1, North-South Street, Hexi District,
Wuhan Konberd Biotech Co., Ltd.

Contact:+86-27-87205925

Address:NO.666, Gaoxin Road, Eastlake High-tech zone
Anhui Asahikasei Chemical Co., Ltd

Contact:86-551-4259770

Address:No. 88 Linquan Road Hefei Anhui 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