H. A. Shea

Total synthesis of marine natural products driven by novel structure, potent biological activity, and/or synthetic methodology.

J. M. Langenhan, R. Rzasa, D. Romo, 2000, Ernst Schering Research Foundation workshop.

Scale-Up Syntheses of Two Naturally Occurring Procyanidins: (−)-Epicatechin-(4β,8)-(+)-catechin and (−)-Epicatechin-3-O-galloyl-(4β,8)-(−)-epicatechin-3-O-gallate†

P. Sharma, H. Schmitz, Alexander G. Kolchinski, 2007 .

Total Synthesis of the Novel, Immunosuppressive Agent (−)-Pateamine A from Mycale sp. Employing a β-Lactam-Based Macrocyclization

R. Rzasa, D. Romo, H. A. Shea, 1998 .

Cp2Fe(PR2)2PdCl2 (R = i-Pr, t-Bu) complexes as air-stable catalysts for challenging Suzuki coupling reactions.

Thomas J. Colacot, T. Colacot, H. A. Shea, 2004, Organic letters.

Total Synthesis and Immunosuppressive Activity of (−)-Pateamine A and Related Compounds: Implementation of a β-Lactam-Based Macrocyclization

Jun O. Liu, J. M. Langenhan, R. Rzasa, 1998 .

Isolation and identification of eukaryotic initiation factor 4A as a molecular target for the marine natural product Pateamine A.

Jun O. Liu, Yongjun Dang, N. Choi, 2007, Methods in enzymology.

Total Synthesis of the Novel, Immunosuppressive Agent (‐)‐Pateamine A from Mycale sp. Employing a β‐Lactam‐Based Macrocyclization.

R. Rzasa, D. Romo, H. A. Shea, 1998 .