Tetrahedron Letters p. 3067 - 3070 (1996)
Update date:2022-09-26
Topics:
Witty, David R.
Walker, Graham
Bateson, John H.
O'Hanlon, Peter J.
Eggleston, Drake S.
Haltiwanger, R. Curtis
The synthesis of conformationally constrained indolmycin analogues is described. Compounds in which the oxazolinone group is separately linked to the indole C-4 position rather than C-3 are also prepared. A highly diastereoselective Michael addition of an
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Doi:10.1021/om00080a005
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