Tetrahedron Letters p. 5063 - 5066 (1999)
Update date:2022-07-30
Topics: Synthesis Catalyst Stereochemistry Chemical reactions Versatile Experimental Electrophilic Functionalised Carbocycles nucleophilic
Ovaa, Huib
Codee, Jeroen D. C.
Lastdrager, Bas
Overkleeft, Herman S.
Van Der Marel, Gijs A.
Van Boom, Jacques H.
A synthetic route towards conduramine and carbasugar derivatives based on the transformation (i.e. two-carbon Wittig olefination and ester reduction) of the Vasella rearrangement product derived from D-galactose followed by either a [3,3] Overman or a [2,3]-Wittig-Still sigmatropic rearrangement, and subsequent ring-closing metathesis, is presented.
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Doi:10.1039/c6ob01686c
(2016)Doi:10.1055/s-1999-2689
(1999)Doi:10.1080/24701556.2020.1789996
(2020)Doi:10.1021/jo010526h
(2001)Doi:10.1021/ja00403a040
(1981)Doi:10.1021/om990014h
(1999)
