J. Busch-Petersen

发表

Synthesis of 15-Deoxy-12-hydroxy-10-(trifluoromethyl)-Delta(7)-PGA(1) Methyl Ester.

M. Tius, J. Kawakami, Huaping Hu, 1998, The Journal of organic chemistry.

Anti‐tumor Promoting Activity of Canventol and Its Synthetic Analogs through Inhibition of Protein Isoprenylation

M. Tius, M. Kerr, A. Komori, 1996, Japanese journal of cancer research : Gann.

A Rhodium(II) catalytic approach to the synthesis of ethers of a minor component in a tautomeric set.

E. Corey, J. Busch-Petersen, 2000, Organic letters.

Inhaled long-acting muscarinic antagonists in chronic obstructive pulmonary disease.

J. Busch-Petersen, Dramane I. Laine, Dramane I. Lainé, 2011, Future medicinal chemistry.

Danirixin: A Reversible and Selective Antagonist of the CXC Chemokine Receptor 2

R. Tal-Singer, J. Foley, R. Mayer, 2017, The Journal of Pharmacology and Experimental Therapeutics.

Tyrosine urea muscarinic acetylcholine receptor antagonists: achiral quaternary ammonium groups.

H. Sarau, J. Foley, Yonghui Wang, 2012, Bioorganic & medicinal chemistry letters.

Design, synthesis and structure-activity relationship of N-substituted tropane muscarinic acetylcholine receptor antagonists.

Zehong Wan, H. Sarau, J. Foley, 2012, Bioorganic & medicinal chemistry letters.

Muscarinic acetylcholine receptor antagonists: SAR and optimization of tyrosine ureas.

Dwight M. Morrow, Wei-Chang Fu, H. Sarau, 2008, Bioorganic & medicinal chemistry letters.

N,N'-Diarylcyanoguanidines as antagonists of the CXCR2 and CXCR1 chemokine receptors.

J. D. Elliott, Wei-Chang Fu, H. Sarau, 2006, Bioorganic & medicinal chemistry letters.

Discovery of potent and orally bioavailable N,N'-diarylurea antagonists for the CXCR2 chemokine receptor.

J. D. Elliott, K. Ward, H. Sarau, 2004, Bioorganic & medicinal chemistry letters.

Unsaturated Side Chain β-11-Hydroxyhexahydrocannabinol Analogs

W. A. Hill, A. Makriyannis, A. Khanolkar, 1996 .

Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalyst

E. Corey, J. Busch-Petersen, M. Horikawa, 1999 .

Small molecule antagonists of the CXCR2 and CXCR1 chemokine receptors as therapeutic agents for the treatment of inflammatory diseases.

J. Busch-Petersen, 2006, Current topics in medicinal chemistry.

Classical/non-classical cannabinoid hybrids; stereochemical requirements for the southern hydroxyalkyl chain.

W. A. Hill, M. Tius, A. Makriyannis, 1995, Life sciences.

Phenol-containing antagonists of the CXCR2 receptor

Yonghui Wang, J. Busch-Petersen, 2008 .

3-Arylamino-2H-1,2,4-benzothiadiazin-5-ol 1,1-dioxides as novel and selective CXCR2 antagonists.

Wei-Chang Fu, H. Sarau, J. Foley, 2007, Bioorganic & medicinal chemistry letters.

Comparison of N,N'-diarylsquaramides and N,N'-diarylureas as antagonists of the CXCR2 chemokine receptor.

K. Ward, H. Sarau, J. Foley, 2007, Bioorganic & medicinal chemistry letters.

Highly Enantioselective Phase Transfer Catalyzed Alkylation of a 3-Oxygenated Propionic Ester Equivalent; Applications and Mechanism

E. Corey, J. Busch-Petersen, A. Bo, 1998 .

Classical/nonclassical hybrid cannabinoids: southern aliphatic chain-functionalized C-6beta methyl, ethyl, and propyl analogues.

M. Tius, A. Makriyannis, P. Fan, 1998, Journal of medicinal chemistry.

New, practical and effective sources of fluoride ion for desilylation to form carbon anions

E. Corey, Yunxin Y Bo, J. Busch-Petersen, 1999 .

Sterically shielded secondary N-tritylamines and N-tritylamide bases, readily available and useful synthetic reagents

E. Corey, J. Busch-Petersen, 2000 .

A Rhodium(II) catalytic approach to the synthesis of ethers of a minor component in a tautomeric set.

E. Corey, J. Busch-Petersen, 2000, Organic letters.

Stereochemical control in the oxymercuration of 5-alken-1-ols

M. Tius, J. Busch-Petersen, 1994 .

Inhibitors of cathepsin C (dipeptidyl peptidase I)

Dramane I Laine, Jakob Busch-Petersen, J. Busch-Petersen, 2010, Expert opinion on therapeutic patents.

Cross-conjugated cyclopentenone prostaglandins synthesis of Δ7-10-chloro-15-deoxy PGA1 ethyl ester

M. Tius, M. Yamashita, J. Busch-Petersen, 1998 .

Discovery of novel and long acting muscarinic acetylcholine receptor antagonists.

Dwight M. Morrow, Wei-Chang Fu, H. Sarau, 2008, Journal of medicinal chemistry.

3,5-Disubstituted-indole-7-carboxamides as IKKβ Inhibitors: Optimization of Oral Activity via the C3 Substituent.

J. Boehm, P. Bamborough, Wei-Chang Fu, 2018, ACS medicinal chemistry letters.

Camphor sulfonamide derivatives as novel, potent and selective CXCR3 antagonists.

Todd L Graybill, H. Sarau, J. Foley, 2009, Bioorganic & medicinal chemistry letters.

Design, synthesis, and structure-activity relationship of tropane muscarinic acetylcholine receptor antagonists.

Zehong Wan, Wei-Chang Fu, H. Sarau, 2009, Journal of medicinal chemistry.

Facile KF/Alumina Mediated Synthesis of α-Heterosubstituted Weinreb Amides

M. Tius, J. Busch-Petersen, 1997 .

Enantioselective synthesis of β-hydroxy-α-amino acid esters by aldol coupling using a chiral quaternary ammonium salt as catalyst

E. Corey, J. Busch-Petersen, M. Horikawa, 1999 .