J. Muhuhi

发表

Development of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactones.

S. Denmark, J. Muhuhi, 2010, Journal of the American Chemical Society.

Mild fluorination of chloropyridines with in situ generated anhydrous tetrabutylammonium fluoride.

Rachel L Merzel, M. Sanford, Laura J. Allen, 2014, The Journal of organic chemistry.

Developing Efficient Nucleophilic Fluorination Methods and Application to Substituted Picolinate Esters

Patrick S. Hanley, M. Sanford, Laura J. Allen, 2014 .

Stereocontrolled total syntheses of isodomoic acids G and H via a unified strategy.

S. Denmark, J. Muhuhi, J. H. Liu, 2011, The Journal of organic chemistry.

Cross-coupling reactions of aromatic and heteroaromatic silanolates with aromatic and heteroaromatic halides.

S. Denmark, Russell C. Smith, J. Muhuhi, 2009, Journal of the American Chemical Society.

Development of a Scalable Process for the Insecticidal Candidate Tyclopyrazoflor. Part 2. Fit-for-Purpose Optimization of the Route to Tyclopyrazoflor Featuring [3 + 2] Cyclization of 3-Hydrazinopyridine·2HCl and Methyl Acrylate

Qiang Yang, Xiaoyong Li, J. Muhuhi, 2019, Organic Process Research & Development.

Expanding the synthetic method and structural diversity potential for the intramolecular Aza Diels-Alder cyclization.

M. Spaller, J. Muhuhi, 2006, The Journal of organic chemistry.

Total syntheses of isodomoic acids G and H.

S. Denmark, J. Muhuhi, J. H. Liu, 2009, Journal of the American Chemical Society.

Design, synthesis and evaluation of a potent substrate analog inhibitor identified by scanning Ala/Phe mutagenesis, mimicking substrate co-evolution, against multidrug-resistant HIV-1 protease.

M. Spaller, Zhigang Liu, I. Kovari, 2013, Biochemical and biophysical research communications.

Design , synthesis and evaluation of a potent substrate-analog peptide-inhibitor identified by scanning Ala / Phe chemical mutagenesis

M. Spaller, Zhigang Liu, I. Kovari, 2013 .