Towards a chemo-enzymatic method for the asymmetric synthesis of β-amino tertiary alcohols
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2009/OB/B916013B
Reference21 articles.
1. Asymmetric Addition to Ketones: Enantioselective Formation of Tertiary Alcohols
2. Asymmetric catalysis for the construction of quaternary carbon centres: nucleophilic addition on ketones and ketimines
3. Alkaloids from a Panamanian Poison Frog, Dendrobates speciosus: Identification of Pumiliotoxin-A and Allo-pumiliotoxin Class Alkaloids, 3,5-Disubstituted Indolizidines, 5-Substituted 8-Methylindolizidines, and a 2-Methyl-6-nonyl-4-hydroxypiperidine
4. New Routes to Clavine-type Ergot Alkaloids. Part 1. First Total Synthesis of Three Natural Products: (+)-Setoclavine, (+)-Isosetoclavine, (-)-9,10-Dihydroisosetoclavine, and Structure Correction of the Latter
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1. Mechanism and Application of Baker–Venkataraman O→C Acyl Migration Reactions;Synthesis;2014-12-02
2. Synthesis of 1,3-Disubstituted Azetidines via a Tandem Ring-Opening Ring-Closing Procedure;Synlett;2012-05-25
3. ChemInform Abstract: Towards a Chemo-Enzymatic Method for the Asymmetric Synthesis of β-Amino Tertiary Alcohols.;ChemInform;2010-04-27
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