Mahmud M. Hussain

发表

Avidity‐mediated virus separation using a hyperthermophilic affinity ligand

Nimish Gera, B. Rao, Ruqi Wang, 2013, Biotechnology progress.

Palladium-catalyzed allylic substitution with (η6-arene-CH2Z)Cr(CO)(3)-based nucleophiles.

P. Carroll, P. Walsh, S. Dreher, 2011, Journal of the American Chemical Society.

Synthesis of piperlogs and analysis of their effects on cells.

S. Schreiber, Drew J. Adams, Z. Boskovic, 2013, Tetrahedron.

Discovery of 8-Membered Ring Sulfonamides as Inhibitors of Oncogenic Mutant Isocitrate Dehydrogenase 1.

S. Schreiber, A. Shamji, G. Dunn, 2016, ACS medicinal chemistry letters.

Tandem reactions for streamlining synthesis: enantio- and diastereoselective one-pot generation of functionalized epoxy alcohols.

P. Walsh, Mahmud M. Hussain, 2008, Accounts of chemical research.

Stereoselective vinylation of aryl N-(2-pyridylsulfonyl) aldimines with 1-alkenyl-1,1-heterobimetallic reagents.

P. Walsh, Mahmud M. Hussain, Muhammed Ziauddin, 2011, Organic letters.

Breaking Conjugation: Unusual Regioselectivity with 2-Substituted Allylic Substrates in the Tsuji-Trost Reaction.

P. Walsh, P. Norrby, Mahmud M. Hussain, 2014, Chemical science.

(R,R) and (S,S)‐N,N‐bis(arylsulfonyl)‐1,2‐cyclohexanediamine

P. Walsh, Mahmud M. Hussain, Deena A.S. Hussain, 2016 .

Applications of 1-alkenyl-1,1-heterobimetallics in the stereoselective synthesis of cyclopropylboronate esters, trisubstituted cyclopropanols and 2,3-disubstituted cyclobutanones.

P. Carroll, P. Walsh, Hongmei Li, 2009, Journal of the American Chemical Society.

Palladium-catalyzed chemoselective allylic substitution, Suzuki-Miyaura cross-coupling, and allene formation of bifunctional 2-B(pin)-substituted allylic acetate derivatives.

P. Walsh, Mahmud M. Hussain, Byeong-Seon Kim, 2014, Chemistry.

Chemo- and diastereoselective tandem dual oxidation of B(pin)-substituted allylic alcohols: synthesis of B(pin)-substituted epoxy alcohols, 2-keto-anti-1,3-diols and dihydroxy-tetrahydrofuran-3-ones

P. Carroll, P. Walsh, Mahmud M. Hussain, 2013 .

Diastereoselective aziridination of 2-B(pin)-substituted allylic alcohols: an efficient approach to novel organoboron compounds.

P. Carroll, P. Walsh, Mahmud M. Hussain, 2011, Organic letters.

Synthesis of 2-keto-anti-1,3-diols by chemoselective tandem oxidation of 2-B(pin)-substituted allylic alcohols.

P. Carroll, P. Walsh, Mahmud M. Hussain, 2011, Angewandte Chemie.

Allylic substitution versus Suzuki cross-coupling: capitalizing on chemoselectivity with bifunctional substrates.

P. Walsh, Mahmud M. Hussain, 2010, Angewandte Chemie.

Discussion Addendum for: Applications of (2S)‐(–)‐3‐exo‐Morpholinoisoborneol [(–)MIB] in Organic Synthesis

P. Walsh, Mahmud M. Hussain, 2014 .

Protein selection using yeast surface display.

Nimish Gera, B. Rao, Mahmud M. Hussain, 2013, Methods.

Highly stable binding proteins derived from the hyperthermophilic Sso7d scaffold.

R. C. Wright, Nimish Gera, B. Rao, 2011, Journal of molecular biology.

Chemical perturbation of an intrinsically disordered region of TFIID distinguishes two modes of transcription initiation

R. Tjian, S. Schreiber, A. Koehler, 2015, eLife.

Small-molecule screening identifies inhibition of salt-inducible kinases as a therapeutic strategy to enhance immunoregulatory functions of dendritic cells

Daniel J. O'Connell, R. Xavier, S. Schreiber, 2014, Proceedings of the National Academy of Sciences.

mRNA display selection and solid‐phase synthesis of Fc‐binding cyclic peptide affinity ligands

Balaji M Rao, Ruben G Carbonell, Stefano Menegatti, 2013, Biotechnology and bioengineering.

Designer proteins that competitively inhibit Gαq by targeting its effector site

B. Kuhlman, J. Sondek, S. Endo-Streeter, 2021, The Journal of biological chemistry.

Engineering a Protein Binder Specific for p38α with Interface Expansion.

B. Kuhlman, S. Angus, Mahmud M. Hussain, 2018, Biochemistry.

Scaffold diversification enhances effectiveness of a superlibrary of hyperthermophilic proteins.

Nimish Gera, Mahmud M. Hussain, B. M. Rao, 2013, ACS synthetic biology.

Niche-Based Screening in Multiple Myeloma Identifies a Kinesin-5 Inhibitor with Improved Selectivity over Hematopoietic Progenitors.

T. Golub, P. Clemons, S. Schreiber, 2015, Cell reports.