Journal of Organic Chemistry p. 6696 - 6700 (1992)
Update date:2022-08-16
Topics:
Wuts, Peter G. M.
Ritter, Allen R.
Pruitt, Lynn E.
The hydroxyethylene isostere of the dipeptide leu-val was synthesized from isovaleryl aldehyde in nine steps in 15percent overall yield without the use of chromatographic separations.A key finding is the ability of an amide to selectively direct an epoxid
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Doi:10.1016/j.bmcl.2016.07.008
(2016)Doi:10.1016/S0040-4039(00)60196-X
(1992)Doi:10.1021/ja4050168
(2013)Doi:10.1002/cmdc.201200484
(2013)Doi:10.1016/j.tetasy.2004.06.015
(2004)Doi:10.1055/s-1992-26279
(1992)
