935475-91-5Relevant academic research and scientific papers
Stereocontrolled Total Synthesis of Nonenolide
Sudina, Purushotham Reddy,Motati, Damoder Reddy,Seema, Aravind
, p. 1399 - 1404 (2018/06/29)
Nonenolide (1) was first isolated from the entomopathogenic fungus Cordyceps militaries BCC2816 and exhibited good antimalarial activity against Plasmodium falciparum K1. Structurally, it features a decanolide with a trans-double bond attached to two chir
Total synthesis of nonenolide
Meshram, Harshadas Mitaram,Kumar, Dachepally Aravind,Ramesh, Palakuri
experimental part, p. 1422 - 1427 (2010/09/12)
A novel synthetic route has been reported for the synthesis of nonenolide. The syntheses of fragments were initiated from commercially available and inexpensive starting materials. The synthesis involves key steps like Sharpless epoxidation, Jacobsen's re
Studies directed toward the first total synthesis of acremodiol and acremonol
Sharma, Gangavaram V.M.,Mallesham, Samala,Chandra Mouli, Chirutha
experimental part, p. 2513 - 2529 (2010/04/03)
Studies directed toward the synthesis of acremodiol and acremonol resulted in the synthesis of two macrodiolides 1, 1a, and 2 besides 3. The attempted synthesis of 1 and 2 confirmed that the absolute stereochemistry defined in the earlier report is incorr
Protecting group directed ring-closing metathesis (RCM): the first total synthesis of an anti-malarial nonenolide
Mohapatra, Debendra K.,Ramesh, Dhondi K.,Giardello, Michael A.,Chorghade, Mukund S.,Gurjar, Mukund K.,Grubbs, Robert H.
, p. 2621 - 2625 (2007/10/03)
The first synthesis of a newly found naturally occurring anti-malarial nonenolide is described. A pivotal step in the synthesis is the ring-closing metathesis of a dienoic ester prepared by coupling an acid and alcohol that were stereoselectively synthesi
