139426-88-3Relevant articles and documents
Studies toward the total synthesis of Cytospolide E
Vadhadiya, Paresh M.,Rout, Jeetendra K.,Ramana
, p. 9088 - 9094 (2015)
In this manuscript, we describe various approaches that we have examined towards the total synthesis of Cytospolide E. We initially attempted the RCM approach employing first and second generation Grubbs and Grubbs-Hoyeda catalysts resulting in the exclus
Direct Entry to 4,10-Didesmethyl (9S)-Dihydroerythronolide A via Catalytic Allene Osmylation
Yu, Libing,Wang, Huan,Akhmedov, Novruz G.,Sowa, Christopher,Liu, Kai,Kim, Hiyun,Williams, Lawrence
, p. 2868 - 2871 (2016/07/06)
Desmethyl erythronolides have emerged as macrolide targets that may prove effective against resistant bacteria. A five-step sequence to 4,10-didesmethyl (9S)-dihydroerythronolide A (1) from known cyclic bis[allene] 13 is reported. Key structural and mechanistic aspects of the synthesis are discussed along with catalytic allene osmylation. An improved route to 13 is also described.
The first stereoselective total synthesis of the Z-isomer of cytospolide e
Yadav,Pandurangam,Suman Kumar,Adi Narayana Reddy,Prasad,Reddy, B.V. Subba,Rajendraprasad,Kunwar
, p. 6048 - 6050 (2012/11/07)
A convergent and highly stereoselective total synthesis of the Z-isomer of cytospolide E has been achieved via Evan's aldol reaction, Sharpless kinetic resolution and RCM cyclisation.