Y. Bolshan

发表

Structure-Based Optimization of a Small Molecule Antagonist of the Interaction Between WD Repeat-Containing Protein 5 (WDR5) and Mixed-Lineage Leukemia 1 (MLL1).

G. Poda, C. Arrowsmith, M. Schapira, 2016, Journal of medicinal chemistry.

Stereoselective Palladium-Catalyzed Arylation of Exo-Glycals with Aryl Iodides.

Y. Bolshan, J. Regier, Supriya Ghanty, 2021, The Journal of organic chemistry.

A Direct Brønsted Acid-Catalyzed Azidation of Benzhydrols and Carbohydrates

Y. Bolshan, R. Maillet, J. Regier, 2019, European Journal of Organic Chemistry.

Bromination of codeine and its derivatives: Revisiting a 95 year old process

Y. Bolshan, S. Barmaki, Jean‐Paul Desaulniers, 2020 .

Enamide synthesis by copper-catalyzed cross-coupling of amides and potassium alkenyltrifluoroborate salts.

R. Batey, Y. Bolshan, 2008, Angewandte Chemie.

Copper-catalyzed cross-coupling of amides and potassium alkenyltrifluoroborate salts: a general approach to the synthesis of enamides

R. Batey, Y. Bolshan, 2010 .

A General Access to Propargylic Ethers through Brønsted Acid Catalyzed Alkynylation of Acetals and Ketals with Trifluoroborates .

Y. Bolshan, Matthew Baxter, 2015, Chemistry.

Metal-free Synthesis of Ynones from Acyl Chlorides and Potassium Alkynyltrifluoroborate Salts

Y. Bolshan, Cassandra Taylor, 2015, Journal of visualized experiments : JoVE.

Metal-free synthesis of ynones from acyl chlorides and potassium alkynyltrifluoroborate salts.

Y. Bolshan, Cassandra Taylor, 2014, Organic letters.

Metal‐Free Derivatization of Benzhydrols with Organosilanes

Y. Bolshan, Mona A. Almaghrabi, 2022, ChemistrySelect.

Nucleophilic displacement at benzhydryl centers: asymmetric synthesis of 1,1-diarylalkyl derivatives.

F. Gosselin, D. Mathre, Cheng-yi Chen, 2004, Organic letters.

A room-temperature protocol for the rhodium(I)-catalyzed addition of arylboron compounds to sulfinimines.

R. Batey, Y. Bolshan, 2005, Organic letters.

A general Brønsted acid-catalyzed allylation of benzhydryl alcohols

Y. Bolshan, Ifedi Orizu, 2016 .

Metal‐Free Alkenylation of Salicylaldehydes with Boronic Acids: Synthesis of Skipped Dienes and 2 H ‐Chromenes

Y. Bolshan, Dylan H. Harris, Renata O. Barichello, 2020 .

Brønsted Acid-Catalyzed Reactions of Trifluoroborate Salts with Benzhydryl Alcohols.

Y. Bolshan, K. Fisher, 2015, The Journal of organic chemistry.

Brønsted Acid-Catalyzed Direct Substitution of 2-Ethoxytetrahydrofuran with Trifluoroborate Salts

Y. Bolshan, K. Fisher, 2016 .

A General Access to Propargylic Ethers Through Broensted Acid Catalyzed Alkynylation of Acetals and Ketals with Trifluoroborates.

Y. Bolshan, Matthew Baxter, 2016 .

Metal-free methodology for the preparation of sterically hindered alkynoylphenols and its application to the synthesis of flavones and aurones

Y. Bolshan, Cassandra Taylor, 2015 .

Thiol on silica as a ‘catch and release’ support for isocyanates to afford ureas

V. Santhakumar, Y. Bolshan, Tomaszewski Miroslaw, 2007 .

Synthesis, Optimization, and Evaluation of Novel Small Molecules as Antagonists of WDR5-MLL Interaction.

G. Poda, C. Arrowsmith, M. Schapira, 2013, ACS medicinal chemistry letters.

Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5

G. Poda, C. Arrowsmith, M. Schapira, 2012, The Biochemical journal.

An allosteric inhibitor of protein arginine methyltransferase 3.

Jian Jin, Matthieu Schapira, Alena Siarheyeva, 2012, Structure.

(R)-β-Lysine-modified Elongation Factor P Functions in Translation Elongation*

M. Ibba, W. Navarre, D. Smil, 2012, The Journal of Biological Chemistry.

Copper-Catalyzed Cross-Coupling of Amides and Potassium Alkenyltrifluoroborate Salts: A General Approach to the Synthesis of Enamides.

R. Batey, Y. Bolshan, 2010 .

Bromo-deaza-SAH: a potent and selective DOT1L inhibitor.

Matthieu Schapira, Wenyu Yu, Wolfram Tempel, 2013, Bioorganic & medicinal chemistry.

Crystal structures of Klebsiella pneumoniae pantothenate kinase in complex with N‐substituted pantothenamides

M. Schapira, D. Smil, Hee-won Park, 2013, Proteins.