Angewandte Chemie - International Edition, volume 51, issue 12, pages 2972-2976

Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents

Laina M. Geary ¹

Sang Kook Woo ¹

Joyce C Leung ¹

Michael J Krische ¹

Hide authors affiliations Show authors affiliations: 1 affiliation

University of Texas at Austin, Department of Chemistry and Biochemistry, 1 University Station – A5300, Austin, TX 78712‐1167 (USA) |

Publication type: Journal Article

Publication date: 2012-02-15

Wiley

Journal: Angewandte Chemie - International Edition

Quartile SCImago

Quartile WOS

Impact factor: 16.6

ISSN: 14337851, 15213773

DOI: 10.1002/anie.201200239

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General Chemistry

Catalysis

Abstract

In the presence of SEGPHOS catalysts, the reaction proceeds generally with high anti-selectivity regardless whether alcohols or aldehydes are used.

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Citations by journals

	2 4 6 8 10 12 14 16 18
Journal of the American Chemical Society	Journal of the American Chemical Society, 17, 17% Journal of the American Chemical Society 17 publications, 17%
Angewandte Chemie - International Edition	Angewandte Chemie - International Edition, 13, 13% Angewandte Chemie - International Edition 13 publications, 13%
Angewandte Chemie	Angewandte Chemie, 13, 13% Angewandte Chemie 13 publications, 13%
Organic Letters	Organic Letters, 11, 11% Organic Letters 11 publications, 11%
Chemical Communications	Chemical Communications, 6, 6% Chemical Communications 6 publications, 6%
Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 4, 4% Advanced Synthesis and Catalysis 4 publications, 4%
Chemistry - A European Journal	Chemistry - A European Journal, 4, 4% Chemistry - A European Journal 4 publications, 4%
ACS Catalysis	ACS Catalysis, 3, 3% ACS Catalysis 3 publications, 3%
Chemical Science	Chemical Science, 3, 3% Chemical Science 3 publications, 3%
Journal of Organic Chemistry	Journal of Organic Chemistry, 2, 2% Journal of Organic Chemistry 2 publications, 2%
Chemical Reviews	Chemical Reviews, 2, 2% Chemical Reviews 2 publications, 2%
Synthesis	Synthesis, 2, 2% Synthesis 2 publications, 2%
Science	Science, 2, 2% Science 2 publications, 2%
Nature Communications	Nature Communications, 2, 2% Nature Communications 2 publications, 2%
Acta crystallographica. Section C, Structural chemistry	Acta crystallographica. Section C, Structural chemistry, 1, 1% Acta crystallographica. Section C, Structural chemistry 1 publication, 1%
Chinese Journal of Organic Chemistry	Chinese Journal of Organic Chemistry, 1, 1% Chinese Journal of Organic Chemistry 1 publication, 1%
Catalysts	Catalysts, 1, 1% Catalysts 1 publication, 1%
Trends in Chemistry	Trends in Chemistry, 1, 1% Trends in Chemistry 1 publication, 1%
Tetrahedron Asymmetry	Tetrahedron Asymmetry, 1, 1% Tetrahedron Asymmetry 1 publication, 1%
ChemCatChem	ChemCatChem, 1, 1% ChemCatChem 1 publication, 1%
ChemInform	ChemInform, 1, 1% ChemInform 1 publication, 1%
Accounts of Chemical Research	Accounts of Chemical Research, 1, 1% Accounts of Chemical Research 1 publication, 1%
Organometallics	Organometallics, 1, 1% Organometallics 1 publication, 1%
RSC Advances	RSC Advances, 1, 1% RSC Advances 1 publication, 1%
Organic Chemistry Frontiers	Organic Chemistry Frontiers, 1, 1% Organic Chemistry Frontiers 1 publication, 1%
Journal of Organometallic Chemistry	Journal of Organometallic Chemistry, 1, 1% Journal of Organometallic Chemistry 1 publication, 1%
Russian Chemical Reviews	Russian Chemical Reviews, 1, 1% Russian Chemical Reviews 1 publication, 1%
	2 4 6 8 10 12 14 16 18

Citations by publishers

	5 10 15 20 25 30 35 40
Wiley	Wiley, 37, 37% Wiley 37 publications, 37%
American Chemical Society (ACS)	American Chemical Society (ACS), 37, 37% American Chemical Society (ACS) 37 publications, 37%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 11, 11% Royal Society of Chemistry (RSC) 11 publications, 11%
Elsevier	Elsevier, 4, 4% Elsevier 4 publications, 4%
Thieme	Thieme, 2, 2% Thieme 2 publications, 2%
American Association for the Advancement of Science (AAAS)	American Association for the Advancement of Science (AAAS), 2, 2% American Association for the Advancement of Science (AAAS) 2 publications, 2%
Springer Nature	Springer Nature, 2, 2% Springer Nature 2 publications, 2%
International Union of Crystallography (IUCr)	International Union of Crystallography (IUCr), 1, 1% International Union of Crystallography (IUCr) 1 publication, 1%
Shanghai Institute of Organic Chemistry	Shanghai Institute of Organic Chemistry, 1, 1% Shanghai Institute of Organic Chemistry 1 publication, 1%
Multidisciplinary Digital Publishing Institute (MDPI)	Multidisciplinary Digital Publishing Institute (MDPI), 1, 1% Multidisciplinary Digital Publishing Institute (MDPI) 1 publication, 1%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 1% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 publication, 1%
	5 10 15 20 25 30 35 40

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Geary L. M. et al. Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents // Angewandte Chemie - International Edition. 2012. Vol. 51. No. 12. pp. 2972-2976.

GOST all authors (up to 50) Copy

Geary L. M., Woo S. K., Leung J. C., Krische M. J. Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents // Angewandte Chemie - International Edition. 2012. Vol. 51. No. 12. pp. 2972-2976.

RIS |

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RIS Copy

TY - JOUR

DO - 10.1002/anie.201200239

UR - https://doi.org/10.1002/anie.201200239

TI - Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents

T2 - Angewandte Chemie - International Edition

AU - Geary, Laina M.

AU - Woo, Sang Kook

AU - Leung, Joyce C

AU - Krische, Michael J

PY - 2012

DA - 2012/02/15 00:00:00

PB - Wiley

SP - 2972-2976

IS - 12

VL - 51

SN - 1433-7851

SN - 1521-3773

ER -

BibTex |

Cite this

BibTex Copy

@article{2012_Geary,

author = {Laina M. Geary and Sang Kook Woo and Joyce C Leung and Michael J Krische},

title = {Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents},

journal = {Angewandte Chemie - International Edition},

year = {2012},

volume = {51},

publisher = {Wiley},

month = {feb},

url = {https://doi.org/10.1002/anie.201200239},

number = {12},

pages = {2972--2976},

doi = {10.1002/anie.201200239}

}

MLA

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MLA Copy

Geary, Laina M., et al. “Diastereo- and Enantioselective Iridium-Catalyzed Carbonyl Propargylation from the Alcohol or Aldehyde Oxidation Level: 1,3-Enynes as Allenylmetal Equivalents.” Angewandte Chemie - International Edition, vol. 51, no. 12, Feb. 2012, pp. 2972-2976. https://doi.org/10.1002/anie.201200239.

Found error?

Publisher

Wiley

Journal

Angewandte Chemie - International Edition

Quartile SCImago

Quartile WOS

Impact factor

16.6

ISSN

14337851 (Print)
15213773 (Electronic)