Open AccessResearch and Development of an Efficient Synthesis of a Key Building Block for Anti-AIDS Drugs by Diphenylprolinol-Catalyzed Enantio- and Diastereoselective Direct Cross Aldol Reaction
Author(s) -
Y Hayashi,
Toshiaki Aikawa,
Yasuharu Shimasaki,
H. Okamoto,
Yosuke Tomioka,
Takashi Miki,
Masahiro Takeda,
Tetsuya Ikemoto
Publication year - 2016
Publication title -
organic process research and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 109
eISSN - 1520-586X
pISSN - 1083-6160
DOI - 10.1021/acs.oprd.6b00178
Subject(s) - aldol reaction , chemistry , aldol condensation , yield (engineering) , furan , organocatalysis , catalysis , nitroaldol reaction , diol , enantioselective synthesis , pyrrolidine , organic chemistry , aldehyde , combinatorial chemistry , materials science , metallurgy
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