Two Prime or not Two PrimeCitation formats

  • Authors:
  • Andrew Spencer
  • Rocio Lopez Rodriguez
  • Igor Larrosa

Standard

Two Prime or not Two Prime. / Spencer, Andrew; Lopez Rodriguez, Rocio ; Larrosa, Igor.

In: Nature Catalysis, Vol. 1, 2018.

Research output: Contribution to journalArticle

Harvard

Spencer, A, Lopez Rodriguez, R & Larrosa, I 2018, 'Two Prime or not Two Prime', Nature Catalysis, vol. 1. https://doi.org/10.1038/s41929-018-0097-2

APA

Spencer, A., Lopez Rodriguez, R., & Larrosa, I. (2018). Two Prime or not Two Prime. Nature Catalysis, 1. https://doi.org/10.1038/s41929-018-0097-2

Vancouver

Spencer A, Lopez Rodriguez R, Larrosa I. Two Prime or not Two Prime. Nature Catalysis. 2018;1. https://doi.org/10.1038/s41929-018-0097-2

Author

Spencer, Andrew ; Lopez Rodriguez, Rocio ; Larrosa, Igor. / Two Prime or not Two Prime. In: Nature Catalysis. 2018 ; Vol. 1.

Bibtex

@article{70e98edec4524c90a56cf65665a7b841,
title = "Two Prime or not Two Prime",
abstract = "The carboxylation of aromatic compounds with CO2 is an attractive reaction, albeit limited in scope. Now, bulky ligands in a Rh(II) catalysed C–H carboxylation of 2-arylphenols are shown to override the standard ortho/para Kolbe-Schmitt-type regioselectivity allowing instead carboxylation at 2’",
author = "Andrew Spencer and {Lopez Rodriguez}, Rocio and Igor Larrosa",
year = "2018",
doi = "10.1038/s41929-018-0097-2",
language = "English",
volume = "1",
journal = "Nature Catalysis",
issn = "2520-1158",
publisher = "Springer Nature",

}

RIS

TY - JOUR

T1 - Two Prime or not Two Prime

AU - Spencer, Andrew

AU - Lopez Rodriguez, Rocio

AU - Larrosa, Igor

PY - 2018

Y1 - 2018

N2 - The carboxylation of aromatic compounds with CO2 is an attractive reaction, albeit limited in scope. Now, bulky ligands in a Rh(II) catalysed C–H carboxylation of 2-arylphenols are shown to override the standard ortho/para Kolbe-Schmitt-type regioselectivity allowing instead carboxylation at 2’

AB - The carboxylation of aromatic compounds with CO2 is an attractive reaction, albeit limited in scope. Now, bulky ligands in a Rh(II) catalysed C–H carboxylation of 2-arylphenols are shown to override the standard ortho/para Kolbe-Schmitt-type regioselectivity allowing instead carboxylation at 2’

U2 - 10.1038/s41929-018-0097-2

DO - 10.1038/s41929-018-0097-2

M3 - Article

VL - 1

JO - Nature Catalysis

JF - Nature Catalysis

SN - 2520-1158

ER -