Stereoselective Synthesis of Acyclic Amino Alcohols via von Braun Ring Opening of Chiral Piperidines
Author:
Affiliation:
1. Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol801123x
Reference31 articles.
1. An efficient synthesis of enantiopure (+)- and (−)-syn-1,3-amino alcohols with a norbornane framework and their application in the asymmetric addition of ZnEt2 to benzaldehyde
2. Regio- and stereoselective synthesis of 1,3-aminoalcohol derivatives from allylamine derivatives via internal sulfinyl group participation
3. A Tandem Semipinacol Rearrangement/Alkylation ofα-Epoxy Alcohols: An Efficient and Stereoselective Approach to Multifunctional 1,3-Diols
4. Asymmetric Synthesis of Protected β-Substituted and β,β-Disubstituted β-Amino Acids Bearing Branched Hydroxyalkyl Side Chains and of Protected 1,3-Amino Alcohols with Three Contiguous Stereogenic Centers from Allylic Sulfoximines and Aldehydes
5. An enantioselective solutions towards synthesizing “skip” 1,3 dimethyl stereocenters. A synthesis of 4S(2E,4R∗,6R∗)-4,6-Dimethyl-2-octenoic acid
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