K. Koch

发表

An improved synthesis of 4-deoxy-4-fluoro-d-galactopyranosyl derivatives

R. J. Chambers, K. Koch, 1993 .

trans-3-Benzyl-4-hydroxy-7-chromanylbenzoic acid derivatives as antagonists of the leukotriene B4 (LTB4) receptor.

B. Dominy, M. Ramchandani, M. Conklyn, 1998, Bioorganic & medicinal chemistry letters.

A Direct Synthesis of Pharmacologically Active ortho-Substituted Biaryls: A Combined Directed Metalation-Palladium Catalyzed Cross Coupling Approach Using Aryl Oxazolines or Benzamides

R. J. Chambers, M. S. Biggers, K. Koch, 1994 .

CP-123,369: A potent, orally active immunosuppressive agent

H. Fouda, D. C. Hanson, L. Melvin, 1995, Inflammation Research.

The SAR of UK-78,282 : A novel blocker of human T cell Kv1.3 potassium channels

R. J. Mather, D. C. Hanson, M. Ramchandani, 1997 .

The SAR of UK-78,282: A Novel Blocker of Human T Cell Kv1.3 Potassium Channels.

R. J. Mather, D. C. Hanson, M. Ramchandani, 1997 .

3-Substituted-4-hydroxy-7-chromanylacetic acid derivatives as antagonists of the leukotriene B4 (LTB4) receptor

E. Laird, L. Melvin, M. Conklyn, 1997 .

Total Synthesis of the Macrolide Antitumor Antibiotic Lankacidin C

A. Kende, Kun Liu, G. Dorey, 1995 .

An investigation of the intramolecular ene reaction of N-acyl imines

F. W. Fowler, K. Koch, J.-M. Lin, 1986 .

Intramolecular radical cyclization of phenolic enolates

A. Kende, K. Koch, Cynthia A. Smith, 1988 .

Total Synthesis of the Macrolide Antitumor Antibiotic Lankacidin C.

A. Kende, Kun Liu, G. Dorey, 1995 .

The Intramolecular Ene Reaction of Carbon-Nitrogen Double Bonds.

F. W. Fowler, K. Koch, Jyh Ming Lin, 1983 .

Preparation of pyrrolidine-based PDE4 inhibitors via enantioselective conjugate addition of alpha-substituted malonates to aromatic nitroalkenes.

J. A. Demattei, P. Nichols, T. Chuang, 2006, Organic letters.

Stereoselective Synthesis of Functionalized Carbocycles and Heterocycles via an Ester Enolate Claisen/Ring-Closing Metathesis Manifold†,‡

A. Termin, John F. Miller, A. Piscopio, 1998 .

Enantioselective total synthesis of lankacidin C

A. Kende, Kun Liu, G. Dorey, 1993 .

An efficient one-pot construction of substituted pyrimidinones

C. Dominguez, M. Bartberger, P. Ibrahim, 2006 .

Intramolecular radical cyclization of phenolic nitronates: Facile synthesis of annelated tropone and tropolone derivatives

A. Kende, K. Koch, 1986 .

Ring closing metathesis in organic synthesis: Evolution of a high speed, solid phase method for the preparation of β-turn mimetics

John F. Miller, A. Piscopio, K. Koch, 1999 .

Solid phase heterocyclic synthesis via ring closing metathesis: Traceless linking and cyclative cleavage through a carbon-carbon double bond☆

John F. Miller, A. Piscopio, K. Koch, 1997 .

Hydroxy-directed hydroaluminations: A stereoselective approach to cycloalkanols from β-aryl enones

J. Smitrovich, K. Koch, 1994 .

Biosynthetic studies of ascomycin (FK520): formation of the (1R,3R,4R)-3,4-dihydroxycyclohexanecarboxylic acid-derived moiety

B. Moore, K. Reynolds, R. Wax, 1994 .

UK‐78,282, a novel piperidine compound that potently blocks the Kv1.3 voltage‐gated potassium channel and inhibits human T cell activation

R. J. Mather, K. Chandy, G. Gutman, 1999, British journal of pharmacology.

Synthetic approaches to 2-(4-hydroxy-7-chromanyl)benzoic acids as antagonists of leukotriene B4.

M. Ramchandani, R. J. Chambers, M. S. Biggers, 1998, Bioorganic & medicinal chemistry letters.

General Preparation of 7-Substituted 4-Chromanones: Synthesis of a Potent Aldose Reductase Inhibitor

M. S. Biggers, K. Koch, 1994 .

Leukotriene B4 plays a critical role in the progression of collagen-induced arthritis.

M. Smith, A. Milici, E. Pettipher, 1995, Proceedings of the National Academy of Sciences of the United States of America.