Amanote Research
Register
Sign In
New Chiral Synthons for Efficient Preparation of Bispropionates via Stereospecific Oxonia-Cope Rearrangements
doi 10.1021/ja061082f.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
New Chiral Synthons for Efficient Introduction of Bispropionates via Stereospecific Oxonia−Cope Rearrangements
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Correction to “New Class of Anion-Accelerated Amino-Cope Rearrangements as Gateway to Diverse Chiral Structures”
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Stereospecific Ring Contraction of Bromocycloheptenes Through Dyotropic Rearrangements via Nonclassical CarbocationAnion Pairs
Stereoselective Synthesis of Allylic Sulfones via the Oxonia-Cope Rearrangement of Homoallylic Alcohols Containing a Homoallylic Sulfone Moiety
A New Efficient Synthesis and Rearrangements of [6]paracyclophane
Chemistry Letters
Chemistry
The Stereospecific Preparation of Trisubstituted Olefins
Chemistry Letters
Chemistry
New Syntheses of Physiologically Active Compounds Using the Chiral Synthons Produced by Microbial or Enzymatic Reactions.
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Organic Chemistry
Efficient Algorithms for Multichromosomal Genome Rearrangements
Journal of Computer and System Sciences
Computer Networks
Applied Mathematics
Communications
Computational Theory
Mathematics
Theoretical Computer Science
Synthesis and Characterisation of Chiral Metallocene Cocatalysts for Stereospecific Α-Olefin Polymerisations