131846-19-0Relevant articles and documents
PROSTANOIDS XXXIII. INVESTIGATION OF THE POSSIBILITIES FOR CHEMOSELECTIVE AND STEREOSELECTIVE REDUCTION OF THE METHYL ESTERS OF (+/-)-1-HOMO-3,4-CIS-DIDEHYDRO-16-PHENOXY(m-CHLOROPHENOXY)-17,18,19,20-TETRANOR-9,15-DIKETO-13,14-TRANS-PROSTENOIC ACIDS
Tolstikov, G. A.,Miftakhov, M. S.,Sidorov, N. S.,Kuchin, A. V.,Spirikhin, L. V.,et al.
, p. 1281 - 1290 (2007/10/02)
Chemoselective and stereoselective reduction of the methyl esters of 1-homo-3,4-cis-didehydro-16-phenoxy(m-chlorophenoxy)-17,18,19,20-tetranor-9,15-diketo-13,14-trans-prostenoic acid by triisobutylaluminum and L-selectride (methylene chloride, -70 deg C) gave the corresponding esters of 11-deoxyprostaglandins of the E and F types.