TOTAL SYNTHESIS OF FK506 AND AN FKBP PROBE REAGENT, (C8,C9-(C-13)2)-FK506

被引：246

作者：

NAKATSUKA, M ^{[1
]}

RAGAN, JA ^{[1
]}

SAMMAKIA, T ^{[1
]}

SMITH, DB ^{[1
]}

UEHLING, DE ^{[1
]}

SCHREIBER, SL ^{[1
]}

机构：

[1] HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1990年 / 112卷 / 14期

关键词：

D O I：

10.1021/ja00170a024

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Asymmetric syntheses of FK506 and (C8,C9-13C2)-FK506 are reported. The latter compound was designed to facilitate an investigation of the interactions between FK506 and its receptor, the recently discovered immunophilin, FKBP. The syntheses involved the preparation of intermediates 7-9 in nonracemic form; the key coupling reactions included a Cram-selective addition of the vinyl Grignard reagent derived from bromide 9 to aldehyde 8 and the addition of the lithioanion of phosphonamide 7 to aldehyde 51, followed by thermal elimination. Dithiane 65 was then hydrolyzed, and glycolic ester 6 (or 6*) was added via an aldol reaction that allowed the introduction of 13C labels at C8 and C9. Elaboration to FK506 proceeded via a Mukaiyama lactamization reaction and a selective deprotection/oxidation sequence, the efficiency of which was critically dependent upon the order of protecting group removal. © 1990, American Chemical Society. All rights reserved.

引用

页码：5583 / 5601

页数：19

共 103 条

[1]

ALTMAN LK, 1989, NY TIMES 1018, V18, P1

[2] TOTAL SYNTHESIS OF PALYTOXIN CARBOXYLIC-ACID AND PALYTOXIN AMIDE [J].