Gregory D. Parker

发表

Synthesis of a novel diarylheptanoid isolated from Zingiber officinale

C. Willis, Gregory D. Parker, Peter T. Seden, 2009 .

Oxonia-cope rearrangement and side-chain exchange in the Prins cyclization.

C. Willis, Gregory D. Parker, J. Harding, 2002, Organic letters.

Probing the mechanism of Prins cyclisations and application to the synthesis of 4-hydroxytetrahydropyrans.

C. Willis, Gregory D. Parker, J. Harding, 2005, Chemical communications.

Stereoselective synthesis of 4-hydroxy-2,3,6-trisubstituted tetrahydropyrans.

C. Willis, Gregory D. Parker, J. Harding, 2003, Organic letters.

Oxonia-Cope Rearrangement and Side-Chain Exchange in the Prins Cyclization.

C. Willis, Gregory D. Parker, J. Harding, 2002 .

Prins cyclizations: labeling studies and application to natural product synthesis.

C. Willis, Gregory D. Parker, J. Harding, 2002, Organic letters.

Pestalotiopsin A. Side chain installation and exhaustive probing of olefin metathesis as a possible tool for elaborating the cyclononene ring.

L. Paquette, Gregory D. Parker, Shuzhi Dong, 2007, The Journal of organic chemistry.

In pursuit of pestalotiopsin a via zirconocene-mediated ring contraction.

L. Paquette, Gregory D. Parker, T. Tei, 2006, Organic letters.

Pestalotiopsin a. Enantioselective construction of potential building blocks derived from antipodal cyclobutanol intermediates.

L. Paquette, Gregory D. Parker, T. Tei, 2007, The Journal of organic chemistry.