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NOVEL, REGIOSELECTIVE ALLYLAMINE CONSTRUCTION - 1ST SYNTHESIS OF GERANYLLINALOISOCYANIDE, A DITERPENE FROM THE MARINE SPONGE, HALICHONDRIA SP
被引:36
作者:
ICHIKAWA, Y
YAMAZAKI, M
ISOBE, M
机构:
[1] Laboratory of Organic Chemistry, School of Agriculture, Nagoya University, Chikusa
来源:
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
|
1993年
/
20期
关键词:
D O I:
10.1039/p19930002429
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The first synthesis of the diterpene, 3-isocyano-3,7,11,15-tetramethylhexadeca-1,6,10,14-tetraene (geranyllinaloisocyanide, 1), has been achieved through an allyl cyanate-to-isocyanate rearrangement. The crucial step in this synthesis is in situ transformation of allyl isocyanates into stable allyl acetamides with trimethylaluminium.
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页码:2429 / 2432
页数:4
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