Search Results - "Jui, N. T"

  • Showing 1 - 6 results of 6
Refine Results
  1. 1

    A practical and scalable system for heteroaryl amino acid synthesis by Aycock, R A, Vogt, D B, Jui, N T

    Published in Chemical science (Cambridge) (2017)
    “…A robust system for the preparation of β-heteroaryl α-amino acid derivatives has been developed using photoredox catalysis. This system operates regiospecific…”
    Get full text
    Journal Article
  2. 2

    A mild catalytic system for radical conjugate addition of nitrogen heterocycles by Aycock, R A, Wang, H, Jui, N T

    Published in Chemical science (Cambridge) (01-04-2017)
    “…The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved a redox radical mechanism that is enabled by limiting the…”
    Get full text
    Journal Article
  3. 3

    A practical and scalable system for heteroaryl amino acid synthesisElectronic supplementary information (ESI) available. See DOI: 10.1039/c7sc03612d by Aycock, R. A, Vogt, D. B, Jui, N. T

    Published 20-11-2017
    “…A robust system for the preparation of β-heteroaryl α-amino acid derivatives has been developed using photoredox catalysis. This system operates via…”
    Get full text
    Journal Article
  4. 4

    A practical and scalable system for heteroaryl amino acid synthesis† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc03612d by Aycock, R. A., Vogt, D. B., Jui, N. T.

    Published in Chemical science (Cambridge) (02-10-2017)
    “…Here, we describe a highly-effective catalytic method for the synthesis of heteroarene-containing unnatural amino acids. A robust system for the preparation of…”
    Get full text
    Journal Article
  5. 5

    A mild catalytic system for radical conjugate addition of nitrogen heterocyclesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7sc00243b by Aycock, R. A, Wang, H, Jui, N. T

    Published 28-03-2017
    “…The direct addition of pyridine and diazine units to electron-poor alkenes has been achieved via a redox radical mechanism that is enabled by limiting the…”
    Get full text
    Journal Article
  6. 6

    A mild catalytic system for radical conjugate addition of nitrogen heterocycles† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc00243b Click here for additional data file by Aycock, R. A., Wang, H., Jui, N. T.

    Published in Chemical science (Cambridge) (13-02-2017)
    “…A catalytic redox system for the direct conjugate addition of pyridines and diazines to Michael acceptors has been developed. The direct addition of pyridine…”
    Get full text
    Journal Article