Synthesis and Structures of Edulan I and II

被引：7

作者：

Adams, David R. ^{[1
]}

Bhatnagar, Surendra P. ^{[1
]}

Cookson, Richard C. ^{[1
]}

Stanley, Gerald ^{[2
]}

Whitfield, Frank B. ^{[2
]}

机构：

[1] Univ Southampton, Dept Chem, Southampton SO9 5NH, Hants, England

[2] CSIRO, Div Food Res, N Ryde, NSW 2113, Australia

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1974年 / 12期

关键词：

D O I：

10.1039/c39740000469

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Edulan I and edulan II have been shown by synthesis to be the stereoisomeric 2,3,5,6-tetrahydro-2,5,5,8a-tetratmethyl-(8aH)-1-benzopyrans (IVa) and (IVb), the configurations of which are established by the results of microhydrogenation.

引用

页码：469 / U12

页数：2