Intramolecular Pictet-Spengler reaction of N(b)-alkoxytryptamines. 4. A study towards diastereocontrol in the synthesis of tetracyclic eudistomins

DOI: 10.1016/S0040-4020(01)80376-8

Source and publish data:

Tetrahedron p. 2325 - 2344 (1993)

Update date:2022-08-03

Topics:

Authors:

Van Maarseveen

Scheeren

Kruse Kruse

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Article abstract of DOI:10.1016/S0040-4020(01)80376-8

The diastereoselectivity of the intramolecular Pictet-Spengler condensation in the synthesis of tetracyclic eudistomins is described. N(b)-Alkoxytryptamines 15a-m were synthesized with different sized groups R². Closure of the 7-membered oxathi

Full text of DOI:10.1016/S0040-4020(01)80376-8

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