Paul A Wender

发表

Function-oriented synthesis, step economy, and drug design.

Paul A Wender, Vishal A Verma, Thomas J Paxton, 2008, Accounts of chemical research.

Art, architecture, and the molecular frontier.

Paul A Wender, P. Wender, 2015, Accounts of chemical research.

Synthesis and biological evaluation of (-)-laulimalide analogues.

Lei Zhang, Paul A Wender, P. Wender, 2003, Organic letters.

Pharmacophore mapping in the laulimalide series: total synthesis of a vinylogue for a late-stage metathesis diversification strategy.

Paul A Wender, P. Wender, S. Mooberry, 2006, Organic letters.

Identification of a tunable site in bryostatin analogs: C20 Bryologs through late stage diversification.

Paul A Wender, P. Wender, J. Baryza, 2005, Organic letters.

Synthesis and PKC binding of a new class of a-ring diversifiable bryostatin analogues utilizing a double asymmetric hydrogenation and cross-coupling strategy.

Paul A Wender, Joshua C Horan, 2006, Organic letters.

Toward the ideal synthesis and molecular function through synthesis-informed design.

Paul A Wender, P. Wender, 2014, Natural product reports.

Total synthesis and initial biological evaluation of new B-ring-modified bryostatin analogs.

Paul A Wender, Vishal A Verma, Vishal A. Verma, 2006, Organic letters.

Total synthesis of (-)-laulimalide.

Lei Zhang, Paul A Wender, P. Wender, 2000, Journal of the American Chemical Society.

Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analogues.

Paul A Wender, A. Mayweg, P. Wender, 2005, Organic letters.

Oligo(serine ester) Charge-Altering Releasable Transporters: Organocatalytic Ring-Opening Polymerization and their Use for in Vitro and in Vivo mRNA Delivery.

Paul A Wender, R. Waymouth, P. Wender, 2019, Journal of the American Chemical Society.

The design, synthesis, and evaluation of C7 diversified bryostatin analogs reveals a hot spot for PKC affinity.

Paul A Wender, Vishal A Verma, Vishal A. Verma, 2008, Organic letters.

Role of the A-ring of bryostatin analogues in PKC binding: synthesis and initial biological evaluation of new A-ring-modified bryologs.

Paul A Wender, P. Wender, M. Clarke, 2005, Organic letters.

A computationally designed Rh(I)-catalyzed two-component [5+2+1] cycloaddition of ene-vinylcyclopropanes and CO for the synthesis of cyclooctenones.

Lei Jiao, Paul A Wender, Dazhi Yang, 2007, Journal of the American Chemical Society.