TY  - JOUR
ID  - pittir18743
UR  - http://d-scholarship-dev.library.pitt.edu/18743/
IS  - 10
A1  - Hoye, AT
A1  - Wipf, P
Y1  - 2011/05/20/
N2  - A convergent route featuring [3,3]-sigmatropic rearrangements of a linchpin azepinopyrrolidine served to install two of the four contiguous stereocenters present in the tricyclic Stemona alkaloids sessilifoliamide and stemoamide. In addition to the first total synthesis of (-)-sessilifoliamide C, a potential biosynthetic relationship between the sessilifoliamides and previously reported Stemona alkaloids is presented. © 2011 American Chemical Society.
JF  - Organic Letters
VL  - 13
SN  - 1523-7060
TI  - Total synthesis of (-)-sessilifoliamide C and (-)-8-epi-stemoamide
SP  - 2634 
AV  - public
EP  -  2637
ER  -