Bioorganic and Medicinal Chemistry Letters p. 3119 - 3122 (1999)
Update date:2022-08-02
Topics:
Cordova, Armando
Reed, Neal N.
Ashley, Jon A.
Janda, Kim D.
Mesylates or tosylates of δ-hydroxy-L-norvaline esters spontaneously afford L-proline esters upon exposure to aqueous buffer in near quantitative yield. This novel reaction has led to the development of a simple route to optically active proline esters.
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Doi:10.1016/S0022-328X(99)00501-X
(1999)Doi:10.3987/COM-05-10335
(2005)Doi:10.1002/cjoc.201400300
(2014)Doi:10.1248/cpb.47.1679
(1999)Doi:10.1016/S0277-5387(99)00285-5
(1999)Doi:10.1016/S0040-4039(01)01118-2
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