4.8 Article

A formal total synthesis of (±)-cephalotaxine using sequential N-acyliminium ion reactions

Journal

ORGANIC LETTERS
Volume 4, Issue 6, Pages 885-888

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol017114f

Keywords

-

Ask authors/readers for more resources

[GRAPHICS] Novel synthesis of cephalotaxine 1 based on tertiary N-acyliminium ion chemistry starting from alkynylamide 2 was achieved. The key steps include the preparation of pyrroloisoquinoline 4 from alkynylamide 2, the ring expansion of pyrroloisoquinoline 4 to pyrrolobenzazepine 12, and the construction of cyclopentapyrrolobenzazepine ring system 6, all of which are derived from N-acyliminium ion intermediates.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available