Diastereoselective Synthesis of a Simplified Core of Rishirilide B.

Autor: Mejorado, Lupe, Pettus, Thomas R. R.
Předmět:
Zdroj: Synthesis; 2006, Vol. 2006 Issue 19, p3209-3214, 6p
Abstrakt: A route enabling the synthesis of the stereo-triad of rishirilide B (1) from 2-hydroxy-3-methylnaphthalene-1,4-dione, is reported. Key transformations include the regioselective 1,2-Grignard addition to a tautomeric mixture of o- and p-quinones, regioselective carbamoylation of a tautomeric mixture, and a synopsis of the methods explored to convert various terminal vinyl ethers into the corresponding carboxylic acid by cleavage. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index