Jump to main content
Jump to site search

Issue 23, 1990
Previous Article Next Article

Synthesis of the staurosporine aglycone

Abstract

The staurosporine aglycone 3 has been synthesised in 22.6% overall yield from ethyl indole-2-acetate by a route which involves an intramolecular Diels–Alder reaction of the pyranoindolone 8 followed by nitrene mediated cyclisation.

Back to tab navigation

Article information


J. Chem. Soc., Chem. Commun., 1990, 1667-1668
Article type
Paper

Synthesis of the staurosporine aglycone

C. J. Moody and K. F. Rahimtoola, J. Chem. Soc., Chem. Commun., 1990, 1667
DOI: 10.1039/C39900001667

Search articles by author

Spotlight

Advertisements