J. P. MARTINEZ

Texas A&M University — United States

Chemistry · Physical Sciences

11h-index807citations21works0.02yr avg
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Research Topics

Asymmetric Synthesis and Catalysis(13), Asymmetric Hydrogenation and Catalysis(7), Synthetic Organic Chemistry Methods(7), Chemical Synthesis and Reactions(4), Molecular spectroscopy and chirality(4)

Publications21 total

ChemInform Abstract: Catalysis by Temporary Covalent Activation. A Novel Catalysis of Unactivated Diels‐Alder Reactions.
ChemInform·1997
Catalysis by temporary covalent activation. A novel catalysis of unactivated Diels-Alder reactions
Tetrahedron Letters·1997· 16 cited
Asymmetric catalytic routes to chiral building blocks of medicinal interest
Pure and Applied Chemistry·1996· 107 citedOpen Access
ChemInform Abstract: Asymmetric Catalytic Synthesis of β‐Branched Amino Acids via Highly Enantioselective Hydrogenation Reactions.
ChemInform·1995· 4 cited
Asymmetric catalytic synthesis of .beta.-branched amino acids via highly enantioselective hydrogenation of .alpha.-enamides.
Journal of the American Chemical Society·1995· 224 cited
ChemInform Abstract: A Versatile Tandem Catalysis Procedure for the Preparation of Novel Amino Acids and Peptides.
ChemInform·1995
ChemInform Abstract: Catalytic Asymmetric Reductive Amination of Ketones via Highly Enantioselective Hydrogenation of the C=N Double Bond.
ChemInform·1994
Catalytic asymmetric reductive amination of ketones via highly enantioselective hydrogenation of the CN double bond
Tetrahedron·1994· 148 cited
ChemInform Abstract: Diels‐Alder Reactions of 2‐Alkenylboranes and cis‐1‐Alkenylboranes. Anomalous Selectivity that Allows a Choice of Regiochemistry.
ChemInform·1993
Diels-Alder reactions of 2-Alkenylboranes and cis-1-alkenylboranes. Anomalous selectivity that allows a choice of regiochemistry
Tetrahedron Letters·1993· 29 cited
ChemInform Abstract: In situ Formation of Vinylboranes for Use in Diels‐Alder Reactions. An Easy One‐Pot Diels‐Alder Synthesis of Cyclohexenols.
ChemInform·1993
ChemInform Abstract: Tuning of Vinylborane Dienophilicity. Optimization of Reactivity, Regioselectivity, endo‐Stereoselectivity, and Reagent Stability.
ChemInform·1992
In situ formation of vinylboranes for use in Diels Alder reactions. An easy one-pot Diels-Alder synthesis of cyclohexenols
The Journal of Organic Chemistry·1992· 53 cited
ChemInform Abstract: Vinylboranes are Omniphilic Dienophiles. Some Unusual and Useful Properties of Vinylboranes in Diels‐Alder Reactions.
ChemInform·1992
ChemInform Abstract: 2‐Trimethylsilylvinylboranes: Highly Reactive and Selective Diels‐ Alder Equivalents of 2‐Trimethylsilylvinyl Alcohol and Acetylene.
ChemInform·1992
Tuning of Vinylborane Dienophilicity. Optimization of Reactivity, Regioselectivity, endo-Stereoselectivity, and Reagent Stability
Tetrahedron·1992· 48 cited
Vinylboranes are omniphilic dienophiles. Some unusual and useful properties of vinylboranes in diels-alder reactions
Tetrahedron Letters·1992· 37 cited
2-Trimethylsilylvinylboranes: highly reactive and selective diels-alder equivalents of 2-trimethylsilylvinyl alcohol and acetylene
Tetrahedron Letters·1991· 45 cited
ChemInform Abstract: High Reactivity, Regioselectivity, and Endo Stereoselectivity of Vinylboranes in Diels‐Alder Reactions.
ChemInform·1991
High reactivity, regioselectivity, and endo-stereoselectivity of vinyl boranes in Diels-Alder reactions
Journal of the American Chemical Society·1990· 74 cited
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Frequent Co-authors

Daniel A. Singleton(14), Mark J. Burk(6), Grace M. Ndip(4), José V. Watson(4), Michael F. Gross(3), John E. Feaster(2), Nick Cosford(1), T. Gregory P. Harper(1), Christopher S. Kalberg(1), J. R. Lee(1), Kyeongsook Kim(1), Alberto Flores‐Martínez(1), Everardo López-Romero(1), Charles E. Bracker(1), José Ruíz-Herrera(1), Salomón Bartnicki-Garcı́a(1), Shun-Wang Leung(1), Yu-Kai Lee(1), S.‐W. LEUNG(1), Y.‐K. LEE(1)