V. Gracias

发表

Ring expansive routes to quinolizidine alkaloids: formal synthesis of (-)-lasubine II.

J. Aubé, V. Gracias, Yibin Zeng, 2003, Organic letters.

Sequential Ugi/Heck cyclization strategies for the facile construction of highly functionalized N-heterocyclic scaffolds

V. Gracias, S. Djurić, J. D. Moore, 2004 .

Synthesis of fused bicyclic imidazoles by sequential van Leusen/ring-closing metathesis reactions.

V. Gracias, S. Djurić, A. Gasiecki, 2005, Organic letters.

Synthesis of fused imidazo azepine derivatives by sequential van Leusen/enyne metathesis reactions

V. Gracias, S. Djurić, A. Gasiecki, 2005 .

Synthesis of fused triazolo-imidazole derivatives by sequential van Leusen/alkyne-azide cycloaddition reactions

V. Gracias, S. Djurić, Daria Darczak, 2005 .

Synthesis of fused imidazole rings by sequential van Leusen/C–H bond activation

V. Gracias, S. Djurić, A. Gasiecki, 2006 .

Synthesis of fused imidazo-pyridine and -azepine derivatives by sequential van Leusen/Heck reactions

X. Beebe, V. Gracias, S. Djurić, 2006 .

Efficient Nitrogen Ring-Expansion Process Facilitated by in Situ Hemiketal Formation. An Asymmetric Schmidt Reaction

Jeffrey Aubé, J. Aubé, V. Gracias, 1995 .

Ring expansion by in situ tethering of hydroxy azides to ketones: The boyer reaction

J. Aubé, V. Gracias, G. Milligan, 1997 .

Efficient Nitrogen Ring‐Expansion Process Facilitated by in situ Hemiketal Formation. An Asymmetric Schmidt Reaction.

J. Aubé, V. Gracias, G. Milligan, 1995 .

Identification of halosalicylamide derivatives as a novel class of allosteric inhibitors of HCV NS5B polymerase.

L. Traphagen, U. Warrior, A. Molla, 2008, Bioorganic & medicinal chemistry letters.

1,4-Dihydroindeno[1,2-c]pyrazoles with acetylenic side chains as novel and potent multitargeted receptor tyrosine kinase inhibitors with low affinity for the hERG ion channel.

S. Davidsen, G. Gintant, Eric F. Johnson, 2007, Journal of medicinal chemistry.

A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2004 .

Regiochemical studies of the ring expansion reactions of hydroxy azides with cyclic ketones.

J. Aubé, V. Gracias, B. T. Smith, 2000, The Journal of organic chemistry.

An efficient one-pot synthesis of substituted 2-arylbenzo[b]thiophene derivatives

V. Gracias, T. Kolasa, Meena V. Patel, 2003 .

A Versatile Synthesis of Fused Triazolo Derivatives by Sequential Ugi/Alkyne—Azide Cycloaddition Reactions.

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2005 .

Synthesis of novel fused isoxazoles and isoxazolines by sequential Ugi/INOC reactions

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2004 .

Synthesis of Fused Triazolo‐Imidazole Derivatives by Sequential van Leusen/Alkyne—Azide Cycloaddition Reactions.

V. Gracias, S. Djurić, Daria Darczak, 2006 .

Nucleophilic addition to iminium ethers in the preparation of functionalized N-alkyl heterocycles.

Jeffrey Aubé, J. Aubé, V. Gracias, 2008, The Journal of organic chemistry.

SYNTHESIS OF FUNCTIONALIZED N-ALKYL HETEROCYCLES FROM KETONES BY A SEQUENTIAL RING EXPANSION/NUCLEOPHILIC ADDITION PROCESS

J. Aubé, V. Gracias, G. Milligan, 1996 .

Synthesis of fused bicyclic imidazoles by sequential van Leusen/ring-closing metathesis reactions.

V. Gracias, S. Djurić, A. Gasiecki, 2005, Organic letters.

Asymmetric Schmidt reaction of hydroxyalkyl azides with ketones.

J. Aubé, V. Gracias, Brenton T Smith, 2003, Journal of the American Chemical Society.

Scaffold oriented synthesis. Part 2: Design, synthesis and biological evaluation of pyrimido-diazepines as receptor tyrosine kinase inhibitors.

Zhiqin Ji, Irini Akritopoulou-Zanze, K. Glaser, 2008, Bioorganic & medicinal chemistry letters.

An expedient route to diaza-spirocycles utilizing a sequential multicomponent α-aminoallylation/ring-closing metathesis strategy

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2006 .

Nucleophilic addition to iminium ethers in the preparation of functionalized N-alkyl heterocycles.

J. Aubé, V. Gracias, Erik Fenster, 2008, The Journal of organic chemistry.

Synthesis of Functionalized N‐Alkyl Heterocycles from Ketones by a Sequential Ring Expansion/Nucleophilic Addition Process.

J. Aubé, V. Gracias, G. Milligan, 1996 .

An Expedient Route to Diaza-Spirocycles Utilizing a Sequential Multicomponent α-Aminoallylation/Ring-Closing Metathesis Strategy.

I. Akritopoulou‐Zanze, V. Gracias, S. Djurić, 2007 .

1,4-Dihydroindeno[1,2-c]pyrazoles as novel multitargeted receptor tyrosine kinase inhibitors.

S. Davidsen, I. Akritopoulou‐Zanze, M. Michaelides, 2006, Bioorganic & Medicinal Chemistry Letters.

An Efficient One‐Pot Synthesis of Substituted 2‐Arylbenzo[b]thiophene Derivatives.

V. Gracias, T. Kolasa, Meena V Patel, 2003 .

A flexible synthesis of privileged structural motifs using the Ollis–Sweeney ammonium ylid rearrangement

Jeffrey L. Cross, R. Henry, V. Gracias, 2008 .