Indolocarbazole nitrogens linked by three-atom bridges: a potent new class of PKC inhibitors

Bioorganic & Medicinal Chemistry Letters
1994.0

Abstract

Two different approaches to preparing a series of potent PKC inhibitors, represented by 11, are delineated, namely, (a) reaction of indolocarbazole derivatives with appropriate 3-atom synthons followed by hydrolysis and/or hydrolysis/reduction or (b) treatment of 2-TIPS Arcyriaflavin A 10 with appropriate 3-atom synthons proceeded by N-Si bond cleavage.

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