SYNTHETIC STUDIES TOWARD (+)-LYSERGIC ACID: CONSTRUCTION OF THE TETRACYCLIC ERGOLINE SKELETON
SYNTHETIC STUDIES TOWARD (+)-LYSERGIC ACID: CONSTRUCTION OF THE TETRACYCLIC ERGOLINE SKELETON
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DOI:
10.3987/com-08-s(d)42
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发表时间:
2009-04-01
期刊:
影响因子:
0.6
通讯作者:
Fukuyama, Tohru
中科院分区:
文献类型:
--
作者:
Inoue, Tohru;Yokoshima, Satoshi;Fukuyama, Tohru
We have successfully constructed the tetracyclic skeleton of lysergic acid, which features an acylation at the C3 position of the indole as well as an intramolecular Heck reaction. The optically active D ring unit could be derived from L-pyroglutamic acid via a disrotatory electrocyclic reaction of a dibromocyclopropane.