138513-24-3Relevant academic research and scientific papers
Free radical 5-exo-dig cyclization as the key step in the synthesis of bis-butyrolactone natural products: Experimental and theoretical studies
Sharma, Gangavaram V. M.,Chary, Devoju Harinada,Chandramouli, Nagula,Achrainer, Florian,Patrudu, Sateesh,Zipse, Hendrik
, p. 4079 - 4084 (2011/06/28)
Radical cyclization reactions were performed by 5-exo-dig mode to yield cis-fused bicyclic systems, leading to the synthesis of bis-butyrolactone class of natural products. The study was aimed at understanding the impact of alkyl side chains of furanoside
STEREOSELECTIVE SYNTHESIS OF THE MIDDLE (C10-C17) AND RIGHT (C18-C30) SEGMENTS, AND THEIR COUPLING TO COMPLETE A FORMAL SYNTHESIS OF THE POLYETHER ANTIBIOTIC SALINOMYCIN
Horita, Kiyoshi,Nagato, Satoshi,Oikawa, Yuji,Yonemitsu, Osamu
, p. 3253 - 3256 (2007/10/02)
The middle (C10-C17) and right (C18-C30) segments of the polyether antibiotic salinomycin were stereoselectively synthesized from D-glucose, D-mannitol, and ethyl L-lactate.Coupling of the two segments followed by construction of the bisketal ring system gave the C10-C30 segment, which was already converted to salinomycin by Kishy.
