Tetrahedron Letters p. 2113 - 2116 (1994)
Update date:2022-09-26
Topics:
Webb, Robert R., II
Barker, Peter L.
Baier, Mark
Reynolds, Mark E.
Robarge, Kirk D.
et al.
The mono-N-alkylation of an anthranylamide derivative via the reductive ring opening of a quinazolinone precursors, enables the synthesis of benzodiazepine dione derivative G5598, a potent inhibitor of the in vitro binding of GpIIbIIIa to fibrinogen.
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