Tetrahedron Letters p. 1197 - 1200 (1985)
Update date:2022-09-26
Topics:
Giese, Bernd
Bartmann, Dieter
The diastereoselectivity of the mercuration of acyclic alkenes 4 can be reversed by changing the substituent in the allylic position; with alcohols the erythro isomers 5 and with esters or hemiacetals the threo isomers 6 and 8 are formed predominantly (Table I).
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Doi:10.1134/S1070428011030274
(2011)Doi:10.1248/cpb.38.1740
(1990)Doi:10.1016/0022-328X(90)85053-2
(1990)Doi:10.1016/S0040-4020(01)81794-4
(1991)Doi:10.1021/jo00311a003
(1990)Doi:10.1007/BF00487429
(1990)
