Diastereoselective anomeric oxygen to carbon rearrangements of silyl enol ether derivatives of lactols.
Lewis acid promoted oxygen to carbon rearrangement of anomerically linked silyl enol ethers gives a new and diastereoselective route to the corresponding 2-α-hydroxyketone substituted products.
المؤلفون الرئيسيون: | Dixon, D, Ley, S, Tate, E |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1998
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مواد مشابهة
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Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of lactols.
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Diastereoselective oxygen to carbon rearrangements of anomerically linked enol ethers and the total synthesis of (+)-(S,S)-(cis-6-methyltetrahydropyran-2-yl)acetic acid, a component of civet
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Highly cis- or trans-selective oxygen to carbon rearrangements of anomerically linked 6-substituted tetrahydropyranyl enol ethers
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Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of furanyl (gamma)- and pyranyl (delta)-lactols.
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A general C-glycosidation procedure via anomeric oxygen to carbon rearrangements of tetrahydropyranyl ether derivatives
حسب: Buffet, M, وآخرون
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