Journal of Organic Chemistry p. 3095 - 3103 (1985)
Update date:2022-08-04
Topics: NMR spectroscopy Chiral Reagents Catalyst Chromatography Syntheses Reaction Conditions Stereospecific Diastereomeric
McCarthy, James R.
Wiedeman, Paul E.
Shuster, Albert J.
Whitten , Jeffrey P.
Barbuch, Robert J.
Huffman, John C
Stereospecific synthetic routes are described for the formation of the three contiguous chiral centers in the four diastereomeric 2-amino-5-phenoxycyclopentanols 1a-4a.All four stereoisomers (1a-4a) were prepared, starting from 3-chlorocyclopentene (6).Am
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Doi:10.1002/hlca.19880710211
(1988)Doi:10.1016/S0020-1693(00)87963-3
(1985)Doi:10.1016/j.tetlet.2015.10.014
(2015)Doi:10.1016/j.tet.2014.07.019
(2014)Doi:10.1021/acs.orglett.8b03104
(2018)Doi:10.1021/jo00218a002
(1985)
