ENANTIOSELECTIVE EPOXIDATION OF CYCLIC 1,3-DIENES CATALYZED BY A STERICALLY AND ELECTRONICALLY OPTIMIZED (SALEN)MN COMPLEX

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Chiral (salen)Mn(m)Cl complexes catalyze epoxidation of cyclic 1,3-dienes with moderate-to-good enantioselectivity. A new catalyst (2), bearing sterically hindered and electron donating OSi(iPr)(3) (OTIPS)substituents, induces up to 12% higher selectivity than the previously-reported tert-butyl substituted analog 1.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
1994-01
Language
English
Article Type
Article
Keywords

EPOXIDES

Citation

TETRAHEDRON LETTERS, v.35, no.5, pp.669 - 672

ISSN
0040-4039
DOI
10.1016/S0040-4039(00)75786-8
URI
http://hdl.handle.net/10203/64207
Appears in Collection
CH-Journal Papers(저널논문)
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