128574-68-5Relevant academic research and scientific papers
Stereoselective Total Synthesis of Polyether Ionophore Antibiotics, Isolasalocid A and Lasalocid A. Part 1. Stereocontrolled Construction of the C Rings (C18-C24) by Acid-Catalyzed Cyclization of p-Methoxyphenylallyl Alcohols
Horita, Kiyoshi,Noda, Ichio,Tanaka, Kazuhiro,Miura, Tamaki,Oikawa, Yuji,Yonemitsu, Osamu
, p. 5979 - 5996 (2007/10/02)
The C18-C24 subunits (11, 12) of isolasalocid A (9) and lasalocid A (10) were synthesized stereoselectively via construction of the tetrahydrofuran and tetrahydropyran rings by acid-catalyzed cyclization of the corresponding p-methoxyphenylallyl alcohols (18, 25). Key words: polyether antibiotic; total synthesis; stereoselective synthesis; tetrahydrofuran; tetrahydropyran; acid-catalyzed cyclization.
SYNTHESIS OF SUBSTITUTED TETRAHYDROFURANS AND TETRAHYDROPYRANS. 2. STEREOCONTROLLED ACID-CATALYZED CYCLIZATIONS
Noda, Ichio,Horita, Kiyoshi,Oikawa, Yuji,Yonemitsu, Osamu
, p. 1917 - 1920 (2007/10/02)
A new acid-catalyzed synthesis of thermodinamically stable 2,5-substituted tetrahydrofurans and 2,6-substituted tetrahydropyrans was developed in order to apply to the synthesis of complex polyether antibiotics.
