Simple synthesis of phenylpropenoid β-D-glucopyranoside congeners based on Mizoroki-Heck type reaction of organoboron reagents

被引：11
作者：
Kishida, M
Akita, H
机构：
[1] Toho Univ, Sch Pharmaceut Sci, Funabashi, Chiba 2748510, Japan
[2] Novartis Pharma KK, Tsukuba Res Inst, Tsukuba, Ibaraki 3002611, Japan
来源：
TETRAHEDRON LETTERS | 2005年 / 46卷 / 23期
关键词：
D O I：
10.1016/j.tetlet.2005.04.023
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Palladium(II)-catalyzed carbon-carbon bond formation between allyl 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranoside (3) and phenylboronic acid congeners gave the phenylpropenoid 2,3,4,6-tetra-O-acetyl-beta-D-glueopyranoside (4a-f) in good.yield. Among them, compounds 4a-c were converted to the naturally occurring phenylpropenoid beta-D-glucopyranoside analogues (1a-c). (c) 2005 Elsevier Ltd. All rights reserved.
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页码：4123 / 4125
页数：3
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