Stereocontrolled reductive amination of 3-hydroxy ketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Stereoselective reduction of β hydroxyketones to 1,3-diols highly selective 1,3-asymmetric induction via boron chelates
2. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride
3. Syntheses via isoxazolines III. Diastereoselective synthesis of γ-amino-alcohols with 2 and 3 chiral centres
4. Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric induction
5. Carbamate-mediated functionalization of unsaturated alcohols. 3. Intramolecular Michael addition of O-carbamates to .alpha.,.beta.-unsaturated esters. A new diastereoselective amination in an acyclic system
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