Synthesis and absolute stereochemistry of roseophilin
The enantiospecific total synthesis of natural roseophilin has been completed in 7.0% overall yield over 15 steps by means of an asymmetric cyclopentannelation. This establishes the absolute configuration of the natural product as 22R,23R. Cyclopentenone
Harrington,Tius
p. 8509 - 8514
(2007/10/03)
More Articles about upstream products of 368423-70-5