Stereocontrolled Transformations oftransα,β‐Aziridine Aldehydes toward Different Amino Hydroxylated Structures
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910500514048
Reference18 articles.
1. The Synthesis of Vicinal Amino Alcohols
2. Synthesis of the C1C10 fragment of the macrolide antibiotic Nystatin A1 from a chiral building block obtained via chemoenzymatic approach
3. Allylation reactions of acylsilanes as synthetic equivalents of aldehydes. Application to a stereocontrolled synthesis of (1S,2S,5S)-(10S)-and-(10R)-allyl myrtanol
4. Efficient Synthesis of Ephedra Alkaloid Analogues Using an Enantiomerically Pure N-[(R)-(+)-α-Methylbenzyl]aziridine-2-carboxaldehyde
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1. Study on the stereochemical control of dihydroxylation of vinyl epoxides and their derivatives;Tetrahedron;2012-04
2. Dimethyl carbonate in the regio- and stereocontrolled opening of three-membered heterocyclic rings;Green Chemistry;2012
3. Novel Stereocontrolled Preparation of Amino Polyols from 2,3-Aziridine Alcohols;Synthetic Communications;2010-05-06
4. Stereocontrolled Transformations of trans α,β-Aziridine Aldehydes Toward Different Amino Hydroxylated Structures.;ChemInform;2006-08-29
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