Enantioselective Synthesis of the Pyrroloquinoline Core of the Martinellines
Organic Letters2000Vol. 2(10), pp. 1395–1397
Citations Over TimeTop 10% of 2000 papers
Abstract
[equation--see text] The first enantioselective synthesis of the martinelline core (-)-3 is reported. The synthesis of (-)-3 from N-allyl-N-(benzyloxycarbonyl)-2-iodoaniline (12) proceeded in seven steps and 23% overall yield. In addition, the preparation of a carbocyclic model system is described.
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