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James P. Morken

James P. Morken

D-Index & Metrics

Chemistry

D-Index
74
Citations
14012
World Ranking
4855
National Ranking
1522

Research.com Recognitions

  • 2002 - Fellow of Alfred P. Sloan Foundation

Overview

James P. Morken is affiliated with Boston College in the United States and has made substantial contributions to the field of chemistry, particularly in organic chemistry. Their research encompasses a wide range of topics including organoboron and organosilicon chemistry, catalytic cross-coupling reactions, and asymmetric hydrogenation and catalysis.

The scientist's work spans several key areas of study, with a focus on:

  • Organoboron and organosilicon chemistry
  • Catalytic Cross-Coupling Reactions
  • Asymmetric Hydrogenation and Catalysis
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Chemical Synthesis and Analysis
  • Catalytic C-H Functionalization Methods

James P. Morken has published extensively across various chemistry subfields, prominently in:

  • Organic Chemistry
  • Materials Chemistry
  • Inorganic Chemistry
  • Molecular Biology
  • Radiology, Nuclear Medicine and Imaging

They have authored numerous papers in notable scientific journals, including multiple publications in the Journal of the American Chemical Society and Angewandte Chemie International Edition. Frequent venues for their work include:

  • Journal of the American Chemical Society
  • The Cambridge Structural Database
  • Angewandte Chemie International Edition
  • Angewandte Chemie
  • Organic Letters

Recent publications illustrate the focus and evolution of their research. These include:

  • α-Boryl Organometallic Reagents in Catalytic Asymmetric Synthesis, 2021, ACS Catalysis
  • Copper-Catalyzed Stereospecific Transformations of Alkylboronic Esters, 2022, Journal of the American Chemical Society
  • Diastereo- and Enantioselective 1,4-Difunctionalization of Borylenynes by Catalytic Conjunctive Cross-Coupling, 2020, Angewandte Chemie International Edition
  • Copper-Catalyzed Coupling of Alkyl Vicinal Bis(boronic Esters) to an Array of Electrophiles, 2022, Journal of the American Chemical Society
  • Catalytic Enantioselective Synthesis of anti-Vicinal Silylboronates by Conjunctive Cross-Coupling, 2020, Angewandte Chemie International Edition

Collaborations appear regularly in their research. Frequent co-authors include:

  • Hao Liang
  • Christophe Allais
  • Robert A. Singer
  • Ziyin Kong
  • Mingkai Zhang

In recognition of their work, James P. Morken was named a Fellow of the Alfred P. Sloan Foundation in 2002.

Best Publications

  • Thermographic Selection of Effective Catalysts from an Encoded Polymer-Bound Library

    Steven J. Taylor;James P. Morken

  • Simple Access to Elusive α-Boryl Carbanions and Their Alkylation: An Umpolung Construction for Organic Synthesis

    Kai Hong;Xun Liu;James P. Morken

  • Catalytic Enantioselective Functionalization of Unactivated Terminal Alkenes

    John R. Coombs;James P. Morken

  • Catalytic conjunctive cross-coupling enabled by metal-induced metallate rearrangement

    Liang Zhang;Gabriel J. Lovinger;Emma K. Edelstein;Adam A. Szymaniak

  • A Catalytic Enantiotopic-Group-Selective Suzuki Reaction for the Construction of Chiral Organoboronates

    Chunrui Sun;Bowman Potter;James P. Morken

  • Direct Stereospecific Amination of Alkyl and Aryl Pinacol Boronates

    Scott N. Mlynarski;Alexander S. Karns;James P. Morken

  • Enantioselective CC and CH Bond Formation Mediated or Catalyzed by Chiral ebthi Complexes of Titanium and Zirconium

    Amir H. Hoveyda;James P. Morken

  • Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling

    Scott N. Mlynarski;Christopher H. Schuster;James P. Morken

  • Reactions of organoboron compounds enabled by catalyst-promoted metalate shifts

    Sheila Namirembe;James P. Morken

  • Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesis

    Heather E. Burks;James P. Morken

  • Rhodium-catalyzed enantioselective diboration of simple alkenes.

    Jeremy B. Morgan;Steven P. Miller;James P. Morken

  • Palladium-catalyzed enantioselective diboration of prochiral allenes.

    Nicholas F. Pelz;Angela R. Woodward;Heather E. Burks;Joshua D. Sieber

  • Synthesis of Vinyl Boronates from Aldehydes by a Practical Boron–Wittig Reaction

    John R. Coombs;Liang Zhang;James P. Morken

  • Nonracemic allylic boronates through enantiotopic-group-selective cross-coupling of geminal bis(boronates) and vinyl halides.

    Bowman Potter;Adam A. Szymaniak;Emma K. Edelstein;James P. Morken

  • Pt-Catalyzed Enantioselective Diboration of Terminal Alkenes with B2(pin)2

    Laura T. Kliman;Scott N. Mlynarski;James P. Morken

  • Development, mechanism, and scope of the palladium-catalyzed enantioselective allene diboration.

    Heather E. Burks;Shubin Liu;James P. Morken

  • Asymmetric 1,4-dihydroxylation of 1,3-dienes by catalytic enantioselective diboration.

    Heather E. Burks;Laura T. Kliman;James P. Morken

  • Rhodium-Catalyzed Enantioselective Reductive Aldol Reaction

    Steven J. Taylor;and Matthew O. Duffey;James P. Morken

  • Catalytic Enantioselective 1,2-Diboration of 1,3-Dienes: Versatile Reagents for Stereoselective Allylation

    Laura T. Kliman;Scott N. Mlynarski;Grace E. Ferris;James P. Morken

  • Enantio- and diastereoselective reductive aldol reactions with iridium-pybox catalysts.

    Cun-Xiang Zhao;Matthew O. Duffey;Steven J. Taylor;James P. Morken

  • Pd-catalyzed enantioselective allyl-allyl cross-coupling.

    Ping Zhang;Laura A. Brozek;James P. Morken

Frequent Co-Authors

Amir H. Hoveyda
Amir H. Hoveyda Boston College
Shubin Liu
Shubin Liu University of North Carolina at Chapel Hill
Stuart L. Schreiber
Stuart L. Schreiber Harvard University
Tarun M. Kapoor
Tarun M. Kapoor Rockefeller University
Tatsuo Ishiyama
Tatsuo Ishiyama Hokkaido University
Peter S. White
Peter S. White University of North Carolina at Chapel Hill
Paul Knochel
Paul Knochel Ludwig-Maximilians-Universität München

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