B. Mudryk

发表

Synthesis of the 6-azaindole containing HIV-1 attachment inhibitor pro-drug, BMS-663068.

Martin D. Eastgate, Christina A. Risatti, Saravanababu Murugesan, 2014, The Journal of organic chemistry.

One-pot synthesis of cyclic enecarbamates from lactam carbamates

B. Mudryk, Jurong Yu, V. Truc, 2005 .

A mechanistic study on the amidation of esters mediated by sodium formamide.

Antonio Ramirez, S. Tummala, B. Mudryk, 2012, The Journal of organic chemistry.

The reaction of carbanions with 2-substituted-2-nitropropanes : Substitution and dimerization occurring by radical chain processes involving electron transfer☆

F. Ros, B. Mudryk, G. A. Russell, 1982 .

Alkylation and oxidative dimerization of enolate anions by radical chain processes

B. Mudryk, G. A. Russell, M. Jawdosiuk, 1981 .

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 1. Evolution of Enabling Strategies

D. Erdemir, Saravanababu Murugesan, R. J. Fox, 2017 .

Adventures in Atropisomerism: Total Synthesis of a Complex Active Pharmaceutical Ingredient with Two Chirality Axes.

Jason M. Stevens, Thomas M. Razler, Antonio Ramirez, 2018, Organic letters.

Vicarious Nucleophilic Substitution in Nitroquinolines1)

M. Mąkosza, B. Mudryk, W. Danikiewicz, 1986 .

Vicarious nucleophilic substitution of hydrogen to the nitro group by tertiary carbanions of α-chloroalkyl phenyl sulphones1

M. Mąkosza, B. Mudryk, 1988 .

Reactions of Organic Anions. Part 134. Vicarious Nucleophilic Substitution in Nitroquinolines.

M. Mąkosza, B. Mudryk, W. Danikiewicz, 1986 .

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 2. Strategic Selections in the Transition from an Enabling Route to a Commercial Synthesis

Bin Zheng, Ke Chen, Martin D. Eastgate, 2017 .

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 5. Selective C-7 Bromination of the 6-Azaindole Core

Richard L. Schild, Martin D. Eastgate, Saravanababu Murugesan, 2017 .

Synthetically useful .beta.-lithioalkoxides from reductive lithiation of epoxides by aromatic radical anions

M. Bhupathy, B. Mudryk, I. Jeong, 1990 .

Development of a Kilogram-Scale Process for the Enantioselective Synthesis of 3-Isopropenyl-cyclohexan-1-one via Rh/DTBM-SEGPHOS-Catalyzed Asymmetric Hayashi Addition Enabled by 1,3-Diol Additives

Thomas M. Razler, Y. Qiu, E. Simmons, 2017 .

A practical synthesis of chloromethyl esters from acid chlorides and trioxane or paraformaldehyde promoted by zirconium tetrachloride

B. Mudryk, N. Soundararajan, S. Rajaraman, 2002 .

Regiochemical control in the reductive cleavage of 2-alkylated oxetanes by use of trialkylaluminums. Tertiary organolithiums with .gamma.-oxy functionality

B. Mudryk, T. Cohen, 1991 .

Synthetically useful dianions via reductive lithiation of tetrahydrofurans by aromatic radical anions

B. Mudryk, T. Cohen, 1991 .

.gamma.-Lithioalkoxides via reductive lithiation of oxetanes by aromatic radical-anions

B. Mudryk, T. Cohen, 1989 .

Generation, rearrangements and some synthetic uses of bishomoallyllithiums

B. Mudryk, T. Cohen, Fangping Chen, 1994 .

Simple one-pot syntheses of spiroketals and oxaspirolactones by addition of .gamma.- and .delta.-cerioalkoxides to lactones and cyclic anhydrides

C. A. Shook, B. Mudryk, T. Cohen, 1990 .

Electron transfer processes. 31. Coupling of enolates of phenones with 2-chloro-2-nitropropane

B. Mudryk, Z. Wróbel, G. A. Russell, 1982 .

Tandem reductive lithiations — Carbanionic cyclizations yielding sulfur stabilized cyclopropyl- and cyclobutylcarbinyllithiums

B. Mudryk, T. Cohen, Fangping Chen, 1999 .

1,3‐Diols from Lithium β‐Lithioalkoxides Generated by the Reductive Lithiation of Epoxides: 2,5‐Dimethyl‐2,4‐Hexanediol

B. Mudryk, T. Cohen, 2003 .

Synthetically Useful β-Lithioalkoxides from Reductive Lithiation of Epoxides by Aromatic Radical Anions.

M. Bhupathy, B. Mudryk, I. Jeong, 1990 .

Generation, some synthetic uses, and 1,2-vinyl rearrangements of secondary and tertiary homoallyllithiums, including ring contractions and A ring expansion. Remarkable acceleration of the rearrangement by an oxyanionic group

B. Mudryk, T. Cohen, 1993 .

Generation, Some Synthetic Uses, and 1,2-Vinyl Rearrangements of Secondary and Tertiary Homoallyllithiums, Including Ring Contractions and A Ring Expansion. Remarkable Acceleration of the Rearrangement by an Oxyanionic Group.

B. Mudryk, T. Cohen, 2010 .

Development of a Robust Process for the Preparation of High-Quality Dicyclopropylamine Hydrochloride

Bin Zheng, Ke Chen, Martin D. Eastgate, 2014 .

Development of a Scalable Synthetic Route to BMS-986251. Part 1: Synthesis of the Cyclohexane Dicarboxylate Fragment

Martin D. Eastgate, Aravind S. Gangu, J. Coombs, 2021 .

A Simple and Efficient Synthesis of Alkyl (2-Nitroaryl)acetates and Alkyl 2-(2-Nitroaryl)propanoates via Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes by Carbanions or Alkyl Chloroacetates of Alkyl 2-Chloropropanoates

B. Mudryk, M. Ma̧kosza, 1988 .

α-Alkylidene Derivatives of β-Diketones and β-Keto Esters; 2-Chloro-2-nitropropane as an Acetone Equivalent in Controlled Cross-Aldol-Type Processes

B. Mudryk, G. A. Russell, M. Jawdosiuk, 1981 .

Development of a Practical Synthesis of a Farnesyltransferase Inhibitor

Junying Fan, B. Mudryk, Zhongping Shi, 2018, Organic Process Research & Development.

An Example of Utilizing Mechanistic and Empirical Modeling in Quality by Design

Alan D. Braem, Srinivas Tummala, Daniel M. Hallow, 2010, Journal of Pharmaceutical Innovation.

One-Pot Conversion of Lactam Carbamates to Cyclic Enecarbamates: Preparation of 1-Tert-Butoxycarbonyl-2,3-Dihydropyrrole

B. Mudryk, Jurong Yu, V. Truc, 2008 .