Synthesis of vinyliodides: progress toward the total synthesis of a jatrophane diterpene

被引：7

作者：

Mohan, Priya ^{[1
]}

Fuertes, Michael J. ^{[1
]}

机构：

[1] Texas Tech Univ, Dept Chem & Biochem, Lubbock, TX 79409 USA

来源：

TETRAHEDRON LETTERS | 2013年 / 54卷 / 30期

关键词：

Vinyl dibromide; Vinyl iodide; Wolkoff's reagent; Tanino-Miyashita olefination; Parikh-Doering oxidation; MULTIDRUG-RESISTANCE; CARBONYL-COMPOUNDS; ALCOHOLS; CONVERSION; OXIDATION; METATHESIS; INHIBITORS; OXIDANT; HALIDES; ALKYNES;

D O I：

10.1016/j.tetlet.2013.05.024

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A noticeable effort toward the total synthesis of a jatrophane diterpene has been made via the synthesis of various vinyliodides utilizing highly stereoselective Tanino-Miyashita olefination reaction; and utilizing the dithiane moiety as an acyl anion equivalent. (C) 2013 Elsevier Ltd. All rights reserved.

引用

页码：3919 / 3925

页数：7

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