S. Urgaonkar

发表

Synthesis of (-)-viriditoxin: a 6,6'-binaphthopyran-2-one that targets the bacterial cell division protein FtsZ.

Jared T. Shaw, J. Fettinger, Charles I. Grove, 2011, Angewandte Chemie.

Separation and characterization of underivatized oligosaccharides using liquid chromatography and liquid chromatography-electrospray ionization mass spectrometry.

D. Armstrong, Y. Liu, J. Verkade, 2005, Journal of chromatography. A.

A highly effective catalyst system for the Pd-catalyzed amination of vinyl bromides and chlorides.

J. Verkade, S. Urgaonkar, Ch. Venkat Reddy, 2005, Organic letters.

Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Stille cross-coupling of aryl chlorides.

W. Su, J. Verkade, S. Urgaonkar, 2004, Organic letters.

Proazaphosphatranes: a highly effective class of triaminophosphine ligands in palladium-catalyzed cross-coupling reactions

S. Urgaonkar, 2004 .

Pd/P(i-BuNCH2CH2)3N: an efficient catalyst for Suzuki cross-coupling of aryl bromides and chlorides with arylboronic acids

J. Verkade, S. Urgaonkar, M. Nagarajan, 2002 .

Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for Stille cross-coupling: coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls.

W. Su, J. Verkade, S. Urgaonkar, 2004, Journal of the American Chemical Society.

Ligand-, copper-, and amine-free sonogashira reaction of aryl iodides and bromides with terminal alkynes.

J. Verkade, S. Urgaonkar, 2004, The Journal of organic chemistry.

Synthesis of antimicrobial natural products targeting FtsZ: (+/-)-dichamanetin and (+/-)-2' ''-hydroxy-5' '-benzylisouvarinol-B.

Henrik Lund, D. Raychaudhuri, H. L. La Pierre, 2005, Organic letters.

Identification and validation of tetracyclic benzothiazepines as Plasmodium falciparum cytochrome bc1 inhibitors.

Bradley I. Coleman, R. Barker, D. Wirth, 2011, Chemistry & biology.

P(i-BuNCH2CH2)3N: an efficient promoter for the nucleophilic aromatic substitution reaction of aryl fluorides with aryl TBDMS (or TMS) ethers.

J. Verkade, S. Urgaonkar, 2005, Organic letters.

Palladium/Proazaphosphatrane‐Catalyzed Amination of Aryl Halides Possessing a Phenol, Alcohol, Acetanilide, Amide or an Enolizable Ketone Functional Group: Efficacy of Lithium Bis(trimethylsilyl)amide as the Base

J. Verkade, S. Urgaonkar, 2004 .

1,8‐Diazabicyclo[5.4.0]undec‐7‐ene

S. Urgaonkar, A. Savoca, 2006 .

P[N(i-Bu)CH2CH2]3N: a versatile ligand for the Pd-catalyzed amination of aryl chlorides.

J. Verkade, S. Urgaonkar, M. Nagarajan, 2003, Organic letters.

Synthesis of N-aryl-aza-crown ethers via Pd-catalyzed amination reactions of aryl chlorides with aza-crown ethers

J. Verkade, S. Urgaonkar, 2004 .

N″′-(1,2-Dimethylethyl)-N,N,N′,N′,N′,N′-hexamethyl Phosphorimidic Triamide†

J. Verkade, S. Urgaonkar, 2007 .

Application of a new bicyclic triaminophosphine ligand in Pd-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides, bromides, and iodides.

Juhua Xu, J. Verkade, S. Urgaonkar, 2003, The Journal of organic chemistry.

Synthesis of kaempferitrin.

S. Urgaonkar, J. Shaw, 2007, The Journal of organic chemistry.

1,5‐Diazabicyclo[4.3.0]non‐5‐ene

S. Urgaonkar, A. Savoca, 2006 .

Discovery and Characterization of Potent Dual P-Glycoprotein and CYP3A4 Inhibitors: Design, Synthesis, Cryo-EM Analysis, and Biological Evaluations.

K. Locher, K. Nosol, M. Smolinski, 2021, Journal of medicinal chemistry.

Discovery of Encequidar, First-in-Class Intestine Specific P-glycoprotein Inhibitor.

M. Smolinski, K. Suh, S. Urgaonkar, 2021, Journal of medicinal chemistry.

Aminoindoles, a Novel Scaffold with Potent Activity against Plasmodium falciparum

Bradley I. Coleman, R. Barker, D. Wirth, 2011, Antimicrobial Agents and Chemotherapy.

A concise silylamine approach to 2-amino-3-hydroxy-indoles with potent in vivo antimalaria activity.

R. Barker, D. Wirth, J. Clardy, 2010, Organic letters.

P(i-BuNCH2CH2)3N: an effective ligand in the palladium-catalyzed amination of aryl bromides and iodides.

J. Verkade, S. Urgaonkar, M. Nagarajan, 2003, The Journal of organic chemistry.

Scope and limitations of Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Buchwald-Hartwig amination reactions of aryl chlorides.

J. Verkade, S. Urgaonkar, 2004, The Journal of organic chemistry.

Scope and Limitations of Pd2(dba)3/P (i-BuNCH2CH2)3N-Catalyzed Buchwald—Hartwig Amination Reactions of Aryl Chlorides.

J. Verkade, S. Urgaonkar, 2005 .

N-Benzyl-3-sulfonamidopyrrolidines as novel inhibitors of cell division in E. coli.

P. Wood, D. Raychaudhuri, T. Mazor, 2007, Bioorganic & medicinal chemistry letters.

Water solubilization of DDGS via derivatization with phosphite esters.

J. Verkade, M. Nandakumar, S. Urgaonkar, 2008, Bioresource technology.

Synthesis of antimicrobial natural products targeting FtsZ: (+/-)-dichamanetin and (+/-)-2' ''-hydroxy-5' '-benzylisouvarinol-B.

Henrik Lund, Jared T Shaw, Sameer Urgaonkar, 2005, Organic letters.

Synthesis of (-)-viriditoxin: a 6,6'-binaphthopyran-2-one that targets the bacterial cell division protein FtsZ.

J. Fettinger, Charles I. Grove, Y. S. Park, 2011, Angewandte Chemie.