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Results: 1-8 |
Results: 8
Stereoselective cyanation of chiral alpha-amino aldehydes by reaction withNagata's reagent: a route to enantiopure beta-amino-alpha-hydroxy acids
Authors: Andres, JM Martinez, MA Pedrosa, R Perez-Encabo, A
Citation: Jm. Andres et al., Stereoselective cyanation of chiral alpha-amino aldehydes by reaction withNagata's reagent: a route to enantiopure beta-amino-alpha-hydroxy acids, TETRAHEDR-A, 12(2), 2001, pp. 347-353
Stereoselective synthesis of (5S,6S)- and (5S,6R)-aza-muricatacin from an L-glutamic acid derivative
Authors: Andres, JM de Elena, N Pedrosa, R Perez-Encabo, A
Citation: Jm. Andres et al., Stereoselective synthesis of (5S,6S)- and (5S,6R)-aza-muricatacin from an L-glutamic acid derivative, TETRAHEDR-A, 12(10), 2001, pp. 1503-1509
Diastereoselective synthesis of enantiopure gamma-amino-beta-hydroxy acidsby Reformatsky reaction of chiral alpha-dibenzylamino aldehydes
Authors: Andres, JM Pedrosa, R Perez, A Perez-Encabo, A
Citation: Jm. Andres et al., Diastereoselective synthesis of enantiopure gamma-amino-beta-hydroxy acidsby Reformatsky reaction of chiral alpha-dibenzylamino aldehydes, TETRAHEDRON, 57(40), 2001, pp. 8521-8530
Tautomerization tendencies of 2-acetylcycloalkanones, 2-acetyl-1,3-cycloalkanediones, and cyclic beta-keto esters of five- and six-membered rings.
Authors: Rojas, A Perez-Encabo, A Herraiz-Sierra, I Blanco, CA
Citation: A. Rojas et al., Tautomerization tendencies of 2-acetylcycloalkanones, 2-acetyl-1,3-cycloalkanediones, and cyclic beta-keto esters of five- and six-membered rings., CAN J CHEM, 79(4), 2001, pp. 448-454
Diastereoselective tandem 6-exo carbolithiation intramolecular ring opening in (-)-8-aminomenthol-derived perhydrobenzoxazines. A new synthesis of enantiopure 1-substituted tetrahydro isoquinolines and 2-azabenzonorbornanes
Authors: Pedrosa, R Andres, C Iglesias, JM Perez-Encabo, A
Citation: R. Pedrosa et al., Diastereoselective tandem 6-exo carbolithiation intramolecular ring opening in (-)-8-aminomenthol-derived perhydrobenzoxazines. A new synthesis of enantiopure 1-substituted tetrahydro isoquinolines and 2-azabenzonorbornanes, J AM CHEM S, 123(9), 2001, pp. 1817-1821
A simple stereoselective synthesis of enantiopure 2-substituted pyrrolidines and piperidines from chiral (R)-phenylglycinol-derived bicyclic 1,3-oxazolidines
Authors: Andres, JM Herraiz-Sierra, I Pedrosa, R Perez-Encabo, A
Citation: Jm. Andres et al., A simple stereoselective synthesis of enantiopure 2-substituted pyrrolidines and piperidines from chiral (R)-phenylglycinol-derived bicyclic 1,3-oxazolidines, EUR J ORG C, (9), 2000, pp. 1719-1726
Synthesis of chiral, non-racemic aldols from chiral beta-hydroxy-Weinreb amides prepared by enantioselective Reformatsky-like reaction induced by chiral beta-aminoalcohols
Authors: Andres, JM Pedrosa, R Perez-Encabo, A
Citation: Jm. Andres et al., Synthesis of chiral, non-racemic aldols from chiral beta-hydroxy-Weinreb amides prepared by enantioselective Reformatsky-like reaction induced by chiral beta-aminoalcohols, TETRAHEDRON, 56(9), 2000, pp. 1217-1223
Efficient synthesis of syn-aziridino alcohols by chelation-controlled addition of dialkylzincs and Grignard reagents to N-benzylaziridino aldehydes
Authors: Andres, JM de Elena, N Pedrosa, R Perez-Encabo, A
Citation: Jm. Andres et al., Efficient synthesis of syn-aziridino alcohols by chelation-controlled addition of dialkylzincs and Grignard reagents to N-benzylaziridino aldehydes, TETRAHEDRON, 55(49), 1999, pp. 14137-14144
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