Journal of Organic Chemistry p. 77 - 81 (1983)
Update date:2022-09-26
Topics:
Freidinger, Roger M.
Hinkle, Jeffery S.
Perlow, Debra S.
Arison, Byron H.
A new two-step synthesis of Fmoc-protected N-alkyl amino acids has been developed.The first step involves acid-catalyzed condensation of an Fmoc-protected amino acid with an aldehyde to form an oxazolidinone.This intermediate is then reduced with triethyl
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Doi:10.1021/ja00344a031
(1983)Doi:10.1002/jlac.198219821210
(1982)Doi:10.1039/c39820001151
(1982)Doi:10.1016/S0040-4039(00)88657-8
(1982)Doi:10.1016/0022-328X(88)80671-5
(1988)Doi:10.2174/157018011793663930
(2011)
