Dehomologation and Ring Contraction Strategies
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9783527830237.ch20
Reference141 articles.
1. Chemical synthesis of 13C labeled anti-HIV nucleosides as mass-internal standards
2. Dehomologation of Aldehydes via Oxidative Cleavage of Silyl Enol Ethers with Aqueous Hydrogen Peroxide Catalyzed by Cetylpyridinium Peroxotungstophosphate under Two-Phase Conditions
3. A multigram, stereoselective synthesis of d-[13C5]ribose from d-[13C6]glucose and its conversion into [13C5]nucleosides
4. Efficient “Dehomologation” of Di-O-isopropylidenehexofuranose Derivatives To Give O-Isopropylidenepentofuranoses by Sequential Treatment with Periodic Acid in Ethyl Acetate and Sodium Borohydride
5. A facile dehomologation of α-substituted aldehydes to the corresponding ketones
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