J. Rico

发表

A convenient procedure for the monosilylation of symmetric 1,n-diols

B. Condon, P. Mcdougal, J. Rico, 1986 .

Peptide mimetic compounds useful as platelet aggregation inhibitors

M. Toth, J. Zablocki, J. Rico, 1993 .

Peptidomimetic antagonists of (cid:1) v (cid:2) 3 inhibit bone resorption by inhibiting osteoclast bone resorptive activity, not osteoclast adhesion to bone

C. Carron, R. Ornberg, W. Westlin, 2000 .

Peptidomimetic antagonists of alphavbeta3 inhibit bone resorption by inhibiting osteoclast bone resorptive activity, not osteoclast adhesion to bone.

C. Carron, R. Ornberg, W. Westlin, 2000, The Journal of endocrinology.

Adenovirus inhibition by peptidomimetic integrin antagonists.

D. Griggs, H. Lu, J. Rico, 2002, Antiviral research.

A novel series of orally active antiplatelet agents.

K. Williams, J. Zablocki, J. Rico, 1995, Bioorganic & medicinal chemistry.

Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp sequence of fibrinogen. (Aminobenzamidino)succinyl (ABAS) series of orally active fibrinogen receptor antagonists.

K. Williams, J. Zablocki, J. Rico, 1995, Journal of medicinal chemistry.

Identification and Characterization of a Novel Δ6/Δ5 Fatty Acid Desaturase Inhibitor As a Potential Anti-Inflammatory Agent

P. Needleman, J. Wendling, A. Raz, 1998 .

Diels-Alder reactions of acyclic chiral alkoxy dienes: Oxygen versus sulfur as an allylic directing group

P. Mcdougal, J. Rico, C. Rojas, 1989 .

Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents.

M. Toth, J. Zablocki, J. Rico, 1994, Bioorganic & medicinal chemistry.

Synthesis of 1,2-cycloalkanediols by intramolecular titanium-induced pinacol coupling

J. Mcmurry, J. Rico, 1989 .

An optimized procedure for titanium-induced carbonyl coupling

J. Mcmurry, T. Lectka, J. Rico, 1989 .

A highly stereoselective Michael addition to an .alpha.,.beta.-unsaturated ester as the crucial step in the synthesis of a novel .beta.-amino acid-containing fibrinogen receptor antagonist

J. Rico, P. Bovy, R. Lindmark, 1993 .

Direct .beta.-lithiation of 2-alkoxy dienes: use in an asymmetric Diels-Alder reaction

D. VanDerveer, P. Mcdougal, J. Rico, 1986 .

Diels-Alder Reactions of Acyclic Chiral Alkoxy Dienes: Oxygen versus Sulfur as an Allylic Directing Group.

P. Mcdougal, J. Rico, C. Rojas, 1990 .

Stereoselective synthesis and .alpha.-lithiation of 1-alkoxy polyenes

P. Mcdougal, J. Rico, 1987 .

Synthesis of novel β-amino acid precursors : β-amino-hydrocoumarins as unusual aspartic acid mimetics used in fibrinogen receptor antagonists

J. Rico, 1994 .

Synthesis and stereochemistry of sarcophytol B: An anticancer cembranoid

J. Mcmurry, J. Rico, Y. Shih, 1989 .

Identification and characterization of a novel delta6/delta5 fatty acid desaturase inhibitor as a potential anti-inflammatory agent.

P. Needleman, J. Wendling, A. Raz, 1998, Biochemical pharmacology.

Orally bioavailable dual MMP-1/MMP-14 sparing, MMP-13 selective alpha-sulfone hydroxamates.

G. Decrescenzo, J. McDonald, T. Boehm, 2010, Bioorganic & medicinal chemistry letters.

R-isomers of Arg-Gly-Asp (RGD) mimics as potent alphavbeta3 inhibitors.

D. Griggs, J. Collins, M. B. Finn, 2007, Bioorganic & medicinal chemistry.