Stereoselective Conjugate Additions of Alcohols to a Chiral (E)-Nitroalkene Derived From (R)-2,3-Isopropylidene Glyceraldehyde
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397910008087321
Reference9 articles.
1. Conjugated nitroalkenes: versatile intermediates in organic synthesis
2. A New Approach to the Synthesis of .beta.-Hydroxy-.alpha.-amino Acids Using (Arylthio)nitrooxiranes
3. 4M lithium perchlorate-nitromethane: An efficient solvent in Diels-Alder reactions using nitroalkenes as dienophiles
4. Dehydratisierung von Nitroaldolen mit Dicyclohexylcarbodiimid: Herstellung von Nitroolefinen unter milden Bedingungen
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1. Synthesis and Comparative Study of Homoisofagomines and Analogues as Glycosidase Inhibitors;European Journal of Organic Chemistry;2013-11-26
2. A versatile and efficient approach for the synthesis of chiral 1,3-nitroamines and 1,3-diamines via conjugate addition to new (S,E)-γ-aminated nitroalkenes derived from L-α-amino acids;Beilstein Journal of Organic Chemistry;2013-04-30
3. Synthesis of furan derivatives of cyclic β-amino acid cispentacin via intramolecular nitrile oxide cycloaddition;Tetrahedron Letters;2012-08
4. An efficient one-pot synthesis of tri-substituted thiophenes via a multicomponent reaction in water;Journal of Sulfur Chemistry;2010-09-28
5. ChemInform Abstract: Stereoselective Conjugate Additions of Alcohols to a Chiral (E)-Nitroalkene Derived from (R)-2,3-Isopropylidene Glyceraldehyde.;ChemInform;2010-06-08
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