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- W2178275019 abstract "A variety of α-C-glycosides may be accessed in an entirely stereoselective fashion from 3-OH glycal esters, by way of the tandem reaction sequence of Tebbe methylenation and Claisen rearrangement. In contrast with previous studies in the corresponding β-series, careful control of conditions for Claisen rearrangement is required in order to avoid loss of integrity of anomeric stereochemistry; thermal rearrangements are best carried out in xylene in a sealed tube." @default.
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- W2178275019 date "2003-07-29" @default.
- W2178275019 modified "2023-09-27" @default.
- W2178275019 title "Synthesis of α-C-Glycosides via Tandem Tebbe Methylenation and Claisen Rearrangement." @default.
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- W2178275019 doi "https://doi.org/10.1002/chin.200330216" @default.
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