Tetrahedron Letters p. 4951 - 4954 (1994)
Update date:2022-07-31
Topics:
Elworthy, Todd R.
Morgans Jr., David J.
Palmer, Wylie S.
Repke, David B.
Smith, David B.
Waltos, Ann Marie
α-Heteroatom substituted orthoesters were prepared and found to undergo the Johnson Claisen rearrangement with a variety of allylic alcohols giving γ,δ-unsaturated α-heteroatom substituted esters in fair to excellent yields. The diastereoselectivity of the process was examined.
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Doi:10.1107/S0108270193013617
(1994)Doi:10.1002/anie.201904702
(2019)Doi:10.1246/cl.1994.1459
(1994)Doi:10.1039/DT9940001963
(1994)Doi:10.1021/acs.joc.7b00550
(2017)Doi:10.1016/0957-4166(94)80106-1
(1994)
