scispace - formally typeset
N

Nicholas Simmons

Researcher at Baylor College of Medicine

Publications -  29
Citations -  776

Nicholas Simmons is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Aryl & Catalysis. The author has an hindex of 12, co-authored 25 publications receiving 576 citations. Previous affiliations of Nicholas Simmons include Janssen Pharmaceutica & University of Pennsylvania.

Papers
More filters
Journal ArticleDOI

Enantioselective Dichlorination of Allylic Alcohols

TL;DR: The development of an enantioselective allylic alcohol dichlorination catalyzed by dimeric cinchona alkaloid derivatives and employing aryl iododichlorides as chlorine sources is reported.
Journal ArticleDOI

Carbonylative Cross-Coupling of ortho-Disubstituted Aryl Iodides. Convenient Synthesis of Sterically Hindered Aryl Ketones

TL;DR: A mild and general protocol for the carbonylative cross-coupling of sterically hindered ortho-disubstituted aryl iodides is reported, which provides an array of substituted biaryl ketones in modest to excellent yield.
Journal ArticleDOI

A Mild, DNA-Compatible Nitro Reduction Using B 2 (OH) 4

TL;DR: A hypodiboric acid system for the reduction of nitro groups on DNA–chemical conjugates has been developed and provided good to excellent yields of the reduced amine product for a variety of functionalized aromatic, heterocyclic, and aliphatic nitro compounds.
Journal ArticleDOI

Quantitative Comparison of Enrichment from DNA-Encoded Chemical Library Selections.

TL;DR: A normalized z-score enrichment metric is proposed using a binomial distribution model that satisfies important criteria that are relevant for analysis of DEL selection data and allows for quantitative comparisons of enrichment of n-synthons from parallel DEL selections.
Journal ArticleDOI

C-N Coupling of DNA-Conjugated (Hetero)aryl Bromides and Chlorides for DNA-Encoded Chemical Library Synthesis.

TL;DR: Conditions utilizing an N-heterocyclic carbene–palladium catalyst are developed that extends this reaction to the coupling of DNA-conjugated (hetero)aromatic chlorides with (heterO)ar automatic and select aliphatic amine nucleophiles to build a 63 million-membered DECL.