Enantiospecific syntheses of pseudopterosin aglycones.: Part 1.: Synthesis of the putative aglycone of pseudopterosin G-J via an A→AB→ABC annulation strategy

被引:26
作者
Chow, R [1 ]
Kocienski, PJ
Kuhl, A
LeBrazidec, JY
Muir, K
Fish, P
机构
[1] Univ Leeds, Dept Chem, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Glasgow, Dept Chem, Glasgow G12 8QQ, Lanark, Scotland
[3] Pfizer Ltd, Cent Res, Sandwich CT13 9NJ, Kent, England
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 2001年 / Royal Society of Chemistry卷 / 19期
关键词
D O I
10.1039/b102960f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The putative aglycone of pseudopterosin G-J and its enantiomer were synthesised enantio specifically from 2,3-dimethoxytoluene and eta (3)-allyl cationic complexes of molybdenum and iron respectively. The A --> AB --> ABC annulation strategy entailed the use of allyl cations or their equivalents for the creation of the three benzylic stereogenic centres. The X-ray structure of tetrahydro naphthalene (-)-41a was determined.
引用
收藏
页码:2344 / 2355
页数:12
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