1204754-02-8Relevant articles and documents
Total synthesis of (6Z,9S)-3,4-trans-9-hydroxy-3-methyldodec-cis-6-en-4-olide and (6Z)-3,4-trans-9-oxo-3-methyldodec-cis-6-en-4-olide γ-butyrolactones
Raju, Galla,Nomula, Rajesh,Ramakrishna, Kallaganti V.S.,Radha Krishna, Palakodety
, p. 6655 - 6657 (2014)
The first total synthesis of (6Z,9S)-3,4-trans-9-hydroxy-3-methyldodec-cis-6-en-4-olide and (6Z)-3,4-trans-9-oxo-3-methyldodec-cis-6-en-4-olide was achieved in a convergent pathway. The salient features of our synthesis include Ohira-Bestmann reaction, regioselective alkyne addition to terminal epoxide, TEMPO/BAIB mediated oxidative lactonization, and partial hydrogenation.
First stereoselective total synthesis of phomonol via oxa-Michael approach
Radha Krishna, Palakodety,Prabhakar, Sunchu
, p. 3788 - 3790 (2013/07/11)
Herein we report the first stereoselective total synthesis of phomonol via Sharpless asymmetric dihydroxylation and 6-exo-trig oxa-Michael addition as the key steps.