Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of furanyl (gamma)- and pyranyl (delta)-lactols.
Tetrahydropyran and tetrahydrofuran containing natural products, drugs and agrochemicals often possess carbon-carbon bonds adjacent to the heteroatom. Consequently, new methods for the construction of anomeric carbon-carbon bonds are of considerable importance. We have devised a new strategy to acce...
المؤلفون الرئيسيون: | Buffet, M, Dixon, D, Ley, S, Reynolds, D, Storer, R |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2004
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مواد مشابهة
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Anomeric oxygen to carbon rearrangements of alkynyl tributylstannane derivatives of lactols.
حسب: Buffet, M, وآخرون
منشور في: (1998) -
Diastereoselective anomeric oxygen to carbon rearrangements of silyl enol ether derivatives of lactols.
حسب: Dixon, D, وآخرون
منشور في: (1998) -
A general C-glycosidation procedure via anomeric oxygen to carbon rearrangements of tetrahydropyranyl ether derivatives
حسب: Buffet, M, وآخرون
منشور في: (1997) -
A total synthesis of (+)-Goniodiol using an anomeric oxygen-to-carbon rearrangement
حسب: Dixon, D, وآخرون
منشور في: (1998) -
Oxygen to carbon rearrangements of anomerically linked alkenols from tetrahydropyran derivatives: an investigation of the reaction mechanism via a double isotopic labelling crossover study
حسب: Buffet, M, وآخرون
منشور في: (2000)