1610046-39-3Relevant academic research and scientific papers
Total synthesis of patulolide A through ring closing metathesis
Subhashini,Bhadraiah,Janaki,Sridhar, Gattu
supporting information, p. 496 - 499 (2018/02/14)
A simple and efficient total synthesis of patulolide A from readily available 7-octen-1-ol is reported by asymmetric synthetic approach. The key reactions involved are asymmetric dihydroxylation using AD-mix-β and Grubbs’ ring-closing metathesis reaction
Total synthesis of antifungal gamahonolide A
Sabitha, Gowravaram,Reddy, K. Purushotham,Reddy, S. Purushotham,Yadav
, p. 3227 - 3228 (2014/06/09)
The first stereoselective total synthesis of gamahonolide A (1) has been accomplished using aminoxylation, Keck allylation, and ring-closing metathesis (RCM) reactions as key steps.
