Absolute configuration of the spiroacetal portion of zooxanthellatoxin-A

DOI: 10.1016/0040-4039(96)01645-0

Source and publish data:

Tetrahedron Letters p. 7267 - 7270 (1996)

Update date:2022-09-26

Topics:

Authors:

Nakamura, Hideshi

Sato, Kuniaki

Murai, Akio

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

Article abstract of DOI:10.1016/0040-4039(96)01645-0

By synthesizing the MTPA ester 11, an enantiomer of the degradation product 1, the absolute configuration of the spiroacetal portion (C79-C95) of zooxanthellatoxin-A was determined to be 81R, 85R, and 93S.

Full text of DOI:10.1016/0040-4039(96)01645-0

Products guided by the article

Product name:tert-Butyl-[(R)-3-(4-methoxy-benzyloxy)-oct-7-enyloxy]-diphenyl-silane

Cas No:183537-00-0

R&D Labs maybe for 183537-00-0

Shenyang Mole pharmaceutical Technology Development Co.,Ltd

Contact:+86-24-31204918/13889278616

Address:No.44, wanliutang road, shenhe District of Shenyang
Tianjin SPHINX SCIENTIFIC LAB.

Contact:+86-022-66211289

Address:Tianda high-tech Park. No.80,the 4th Avenue
ZHEJIANG SYNOSE TECH CO.,LTD.

website:https://www.synose.com/

Contact:86-579-82275537

Address:No.1958 Liyu Road , jinhua,zhejiang,China
Shanghai Science Peptide Biological Technology Co.,ltd

website:http://www.scipeptide.com

Contact:+86-21-51099675

Address:No.8 Changyang Rd
HANWAYS CHEMPHARM CO.,LIMITED

website:http://www.hanwayschem.com

Contact:+86-18502787239(whatsapp)-

Address:18-1-802, Green Garden, Jianghan District, Wuhan 430023, China

Relevant to this article

Non-peptidic inhibitors of human chymase. Synthesis, structure-activity relationships, and pharmacokinetic profiles of a series of 5-amino-6-oxo-1,6-dihydropyrimidine-containing trifluoromethyl ketones

Doi:10.1016/S0968-0896(00)00244-3
(2001)
Formation of silyloxy-substituted pyrrolizidinones, indolizidinones and quinolizidinones via intramolecular cyclizations of α-acylamino radicals with acylsilanes

Doi:10.1039/CC9960002469
(1996)
Addition of an apiosyl radical to activated olefins - Synthesis of C-apiosyl compounds

Doi:10.1055/s-1996-4407
(1996)
Doi:10.1007/BF00911437
()
A convenient way to N-allyloxycarbonyl protected adenosine and cytidine derivatives

Doi:10.1055/s-1998-1822
(1998)
An efficient method for catalytic stereoselective synthesis of α-L-fucopyranosides

Doi:10.1246/cl.1996.1123
(1996)

Article Doi