Selective Inversion of the Proximal or Distal Hydroxyl Groups in syn,syn-3-[N-(Alkoxycarbonyl)amino] 1,2-Diols via Cyclic Sulfates
Author:
Affiliation:
1. Department of Chemistry, University of California, Berkeley, California 94720
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961060j
Reference50 articles.
1. Pinacol Cross Coupling of 2-[N-(Alkoxycarbonyl)amino] Aldehydes and Aliphatic Aldehydes by [V2Cl3(THF)6]2[Zn2Cl6]. Synthesis of syn,syn-3-[N-(Alkoxycarbonyl)amino] 1,2-Diols
2. Intermolecular pinacol cross coupling of electronically similar aldehydes. An efficient and stereoselective synthesis of 1,2-diols employing a practical vanadium(II) reagent
3. Intermolecular pinacol cross coupling of aryl aldehydes or their dimethyl acetals with non-aryl aldehydes
4. A stereospecific synthesis of 3,3-disubstituted allylic alcohols. The intermolecular pinacol cross-coupling reaction between .alpha.,.alpha.-disubstituted .alpha.-(diphenylphosphinoyl)acetaldehydes [Ph2P(O)CR1R2CHO] and saturated aldehyde
5. Stereoselective synthesis of 3-amino 1,2-diols via intermolecular pinacol cross-coupling of .alpha.-[(alkoxycarbonyl)amino] aldehydes with aliphatic aldehydes. Short asymmetric syntheses of two 2,3,6-trideoxy-3-amino sugars
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