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Stereoselective synthesis of the indolizinoindole ring system

โœ Scribed by Steven M. Allin; Christopher I. Thomas; James E. Allard; Matthew Duncton; Mark R.J. Elsegood; Mark Edgar

Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
140 KB
Volume
44
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

We report a novel, facile and stereoselective approach to the indolizino[8,7-b]indole ring system from a readily available, non-racemic chiral template.

๐Ÿ“œ SIMILAR VOLUMES

A novel stereoselective synthesis of the
A novel stereoselective synthesis of the ring AB podocarpate system
โœ Ling Lu; Richard K. Shoemaker; Desmond M.S. Wheeler ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 209 KB

A new way of stereoselectively synthesizing rings A and B of podocarpate has been developed; the correct stereochemistry at C, is obtained during a cyclization linking Cz to C,. Although members of the family of norditerpenoid dilactones that includes inumakilactones, podolactones, nagilactones, pod