STEREOSELECTIVE INTRAMOLECULAR ENONE-OLEFIN PHOTOCYCLOADDITIONS OF 1,7-DIENES - MODEL STUDIES ON THE SYNTHESIS OF LYCOPODIUM ALKALOIDS

被引：19

作者：

CRIMMINS, MT

WATSON, PS

机构：

[1] Venable and Kenan Laboratories, Chemistry University of North Carolina at Chapel Hill, Chapel Hill

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 02期

基金：

美国国家科学基金会;

关键词：

STEREOSELECTIVE PHOTOCYCLOADDITIONS; LYCOPODIUM ALKALOIDS; HOMOENOLATE;

D O I：

10.1016/S0040-4039(00)60546-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The synthesis and stereoselective intramolecular [2+2] photocycloaddition reactions of enones 4a and 4s has been accomplished, yielding possible precursors for the development of a total synthesis of several lycopodium alkaloids.

引用

页码：199 / 202

页数：4

共 14 条

[11] SHARPLESS KB, 1980, J AM CHEM SOC, V102, P5976
[12] CYCLOPENTANNULATION WITH A 1,3-DICARBONYL DIPOLE EQUIVALENT - SYNTHESIS OF BICYCLO[3.3.0]OCT-1(5)-ENE-2,6-DIONE
STLAURENT, DR
PAQUETTE, LA
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (20) : 3861 - 3864
[13] A STEREOSELECTIVE SYNTHESIS OF THE AZASPIROUNDECANE RING-SYSTEM OF (-)-HISTRIONICOTOXIN FROM (+)-GLUTAMIC ACID
WINKLER, JD
HERSHBERGER, PM
SPRINGER, JP
[J]. TETRAHEDRON LETTERS, 1986, 27 (43) : 5177 - 5180
[14] YADAV JS, 1990, TETRAHEDRON, V46, P7033

← 1 2 →