Tetrahedron Letters p. 5505 - 5508 (1998)
Update date:2022-08-03
Topics:
Boaz, Neil W.
High enantioselectivity has been observed for the catalytic asymmetric hydrogenation of enol esters bearing a vinylic (≤94% ee) or acetylenic (>97% ee) substituent using a rhodium-chiral bisphosphine catalyst. This is at variance with the hydrogenation of enol esters bearing a saturated substituent, which are hydrogenated with only moderate enantioselectivity under the same conditions.
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Doi:10.1021/ma3016135
(2012)Doi:10.1016/S0040-4039(98)01115-0
(1998)Doi:10.1039/a804385j
(1998)Doi:10.1016/j.ejmech.2018.06.047
(2018)Doi:10.1021/ja980724z
(1998)Doi:10.1016/S0040-4020(98)00609-7
(1998)
