Tetrahedron Letters p. 723 - 726 (1982)
Update date:2022-08-04
Topics:
Albaugh-Robertson, Pamela
Katzenellenbogen, John A.
Ethyl 3-methyl-2-trimethylsilyl-3-butenoate (3) undergoes reaction selectively at carbon 4, upon treatment with a Lewis acid and carbonyl compounds, acetals, ketals, acid chlorides, and chloromethyl phenyl sulfide.This overall conversion represents a high
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Doi:10.1002/ardp.19823150618
(1982)Doi:10.1271/bbb1961.46.1277
(1982)Doi:10.1016/S0020-1693(00)91178-2
(1982)Doi:10.1016/S0960-894X(96)00492-1
(1996)Doi:10.1007/BF00506156
(1982)Doi:10.1055/s-1982-29818
(1982)
