J. Sundeen

发表

The reaction of 3-propylindole with aldehydes preparation of 2-(α-aminoalkyl) indoles

J. Wolinsky, J. Sundeen, 1970 .

The synthesis of the fungal sex hormone antheridiol.

J. Fried, J. Edwards, J. Mills, 1969, Journal of the American Chemical Society.

A new synthetic route to the fungal sex hormone antheridiol and the determination of its absolute stereochemistry

T. Iwadare, J. Fried, W. Salmond, 1972 .

A General Large Scale Synthesis of 2-Alkyl-7-methoxyindoles

K. Leftheris, A. P. Skoumbourdis, J. Hynes, 2001 .

Vicarious nucleophilic substitution of 1-benzyl-5-nitroimidazole, application to the synthesis of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one

Saleem Ahmad, S. Chao, John E. Tellew, 2002 .

Nucleophilic aromatic substitution of methacrylamide anion and its application to the synthesis of the anticancer drug bicalutamide.

J. Barrish, M. Salvati, Bang-Chi Chen, 2003, The Journal of organic chemistry.

BMS-200475, a novel carbocyclic 2′-deoxyguanosine analog with potent and selective anti-hepatitis B virus activity in vitro

O. Kocy, M. Young, R. Colonno, 1997 .

A new facile method for the synthesis of 1-arylimidazole-5-carboxylates

Ping Chen, J. Barrish, Zhongqi Shen, 2000 .

A new facile synthesis of 2-aminothiazole-5-carboxylates

Bang-Chi Chen, R. Zhao, J. Sundeen, 2001 .

Novel triethylsilane mediated reductive N-alkylation of amines: improved synthesis of 1-(4-imidazolyl)methyl-4-sulfonylbenzodiazepines, new farnesyltransferase inhibitors

P. Guo, Bang-Chi Chen, R. Zhao, 2001 .

On the facile dehydrohalogenation of amino acid derived chloromethyl ketones.

E. Gordon, S. Natarajan, J. Pluščec, 1984 .

A Facile Method for the Transformation of N-(tert-Butoxycarbonyl) α-Amino Acids to N-Unprotected α-Amino Methyl Esters

O. Kocy, G. Vite, A. P. Skoumbourdis, 1999 .

A new highly enantioselective synthesis of both (R)- and (S)-2-mercaptosuccinic acids

O. Kocy, Bang-Chi Chen, M. Bednarz, 1998 .

A new strategy for the construction of the imidazo[1,5-a]quinoxalin-4-one ring system and its application to the efficient synthesis of BMS-238497, a novel and potent Lck inhibitor.

J. Barrish, Bang-Chi Chen, R. Zhao, 2004, The Journal of organic chemistry.

Efficient Molar-Scale Synthesis of 1-Methyl-5-acylimidazole Triflic Acid Salts

A. P. Skoumbourdis, Bang-Chi Chen, S. Traeger, 2000 .

Synthesis of deuterium-labeled atorvastatin and its metabolites for use as internal standards in a LC/MS/MS method developed for quantitation of the drug and its metabolites in human serum

M. Jemal, P. Guo, Bang-Chi Chen, 2000 .

Synthesis and antiviral activity of novel isonucleoside analogs.

S. Spergel, J. Clark, J. Tino, 1993, Journal of medicinal chemistry.

PROCEDE DE PREPARATION AMELIORE DE L'AGENT ANTIVIRAL [1S-(1α, 3α, 4β)]-2-AMINO-1,9-DIHYDRO-9-[4-HYDROXY-3-(HYDROXYMETHYL)-2-METHYLENE-CYCLOPENTYL]-6-H-PURINE-6-ONE

G. Bisacchi, J. Sundeen, 1997 .

Pharmacokinetics and antiviral activity of a novel isonucleoside, BMS-181165, against simian varicella virus infection in African green monkeys.

J. Clark, K. Soike, J. Russell, 1994, Antiviral research.

Efficient Molar‐Scale Synthesis of 1‐Methyl‐5‐acylimidazole Triflic Acid Salts.

A. P. Skoumbourdis, Bang-Chi Chen, G. Rovnyak, 2001 .

Response of Achyla ambisexualis e87 to the Hormone Antheridiol and Certain Other Steroids

R. Seshadri, T. Mcmorris, T. Arunachalam, 1974 .

A Facile Method for the Transformation of N-(tert-Butoxycarbonyl) α-Amino Acids to N-Unprotected α-Amino Methyl Esters.

O. Kocy, G. Vite, P. Guo, 2000 .

Nondepressant beta-adrenergic blocking agents. 1. Substituted 3-amino-1-(5,6,7,8-tetrahydro-1-naphthoxy)-2-propanols.

V. Narayanan, C. Cimarusti, M. Condon, 1978, Journal of medicinal chemistry.

A new efficient synthesis of N-(2-(2-(3-methoxy-4-(oxazol-5-yl)phenylamino)oxazol-5-yl)phenyl)-N-methyl-2-morpholinoacetamide (BMS-337197), A novel IMPDH inhibitor

E. Iwanowicz, J. Barrish, A. P. Skoumbourdis, 2007 .

Synthesis of d3-cerivastatin for use as internal standard in a LC/MS/MS method developed for quantitation of the drug in human serum

J. Barrish, M. Jemal, J. Robl, 2006 .