Angewandte Chemie - International Edition

, volume 56 , issue 23 , pages 6604-6608

A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles

Jennifer L Meloche ¹

Brandon L Ashfeld ¹

Hide authors affiliations Show authors affiliations: 1 affiliation

Department of Chemistry and Biochemistry University of Notre Dame Notre Dame IN 46556 USA |

Publication type: Journal Article

Publication date: 2017-05-03

Wiley

Angewandte Chemie - International Edition

scimago Q1

wos Q1

SJR: 5.550

CiteScore: 27.6

Impact factor: 16.9

ISSN: 14337851, 15213773

DOI: 10.1002/anie.201701147

Copy DOI

PubMed ID: 28466963

General Chemistry

Catalysis

Abstract

Put a ring on it: The title reaction between diazooxindoles as electrophilic C1 synthons and 1,3-heterodienes enables the construction of spirooxindole pyrrolones. Employing vinyl isocyanates as 1,4-dipoles, the cycloannulation occurs under relatively mild conditions and provides the corresponding pyrrolones in good to excellent yields.

Found

1 citation

Bezzubov Stanislav

PhD in Chemistry

89 publications, 639 citations, 24 reviews

h-index: 15

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Research interests

"Smart" materials

Coordination Chemistry

Crystal Chemistry

1 citation

Skvortsov Dmitry

🥼

PhD in Chemistry

128 publications, 1 871 citations, 1 review

h-index: 26

Lomonosov Moscow State University

Top-30

Journals

	1 2 3 4 5 6 7
Organic Letters	Organic Letters, 7, 13.46% Organic Letters 7 publications, 13.46%
Journal of Organic Chemistry	Journal of Organic Chemistry, 6, 11.54% Journal of Organic Chemistry 6 publications, 11.54%
Chemical Communications	Chemical Communications, 6, 11.54% Chemical Communications 6 publications, 11.54%
Asian Journal of Organic Chemistry	Asian Journal of Organic Chemistry, 3, 5.77% Asian Journal of Organic Chemistry 3 publications, 5.77%
Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 3, 5.77% Advanced Synthesis and Catalysis 3 publications, 5.77%
Organic Chemistry Frontiers	Organic Chemistry Frontiers, 3, 5.77% Organic Chemistry Frontiers 3 publications, 5.77%
Nature Communications	Nature Communications, 2, 3.85% Nature Communications 2 publications, 3.85%
Synthesis	Synthesis, 2, 3.85% Synthesis 2 publications, 3.85%
Beilstein Journal of Organic Chemistry	Beilstein Journal of Organic Chemistry, 1, 1.92% Beilstein Journal of Organic Chemistry 1 publication, 1.92%
Chinese Journal of Catalysis	Chinese Journal of Catalysis, 1, 1.92% Chinese Journal of Catalysis 1 publication, 1.92%
Tetrahedron Letters	Tetrahedron Letters, 1, 1.92% Tetrahedron Letters 1 publication, 1.92%
Coordination Chemistry Reviews	Coordination Chemistry Reviews, 1, 1.92% Coordination Chemistry Reviews 1 publication, 1.92%
Angewandte Chemie	Angewandte Chemie, 1, 1.92% Angewandte Chemie 1 publication, 1.92%
Angewandte Chemie - International Edition	Angewandte Chemie - International Edition, 1, 1.92% Angewandte Chemie - International Edition 1 publication, 1.92%
Helvetica Chimica Acta	Helvetica Chimica Acta, 1, 1.92% Helvetica Chimica Acta 1 publication, 1.92%
ACS Catalysis	ACS Catalysis, 1, 1.92% ACS Catalysis 1 publication, 1.92%
RSC Advances	RSC Advances, 1, 1.92% RSC Advances 1 publication, 1.92%
Chemical Science	Chemical Science, 1, 1.92% Chemical Science 1 publication, 1.92%
Organic and Biomolecular Chemistry	Organic and Biomolecular Chemistry, 1, 1.92% Organic and Biomolecular Chemistry 1 publication, 1.92%
New Journal of Chemistry	New Journal of Chemistry, 1, 1.92% New Journal of Chemistry 1 publication, 1.92%
Synlett	Synlett, 1, 1.92% Synlett 1 publication, 1.92%
Topics in Current Chemistry	Topics in Current Chemistry, 1, 1.92% Topics in Current Chemistry 1 publication, 1.92%
European Journal of Inorganic Chemistry	European Journal of Inorganic Chemistry, 1, 1.92% European Journal of Inorganic Chemistry 1 publication, 1.92%
Frontiers in Chemistry	Frontiers in Chemistry, 1, 1.92% Frontiers in Chemistry 1 publication, 1.92%
Scientia Sinica Chimica	Scientia Sinica Chimica, 1, 1.92% Scientia Sinica Chimica 1 publication, 1.92%
Mendeleev Communications	Mendeleev Communications, 1, 1.92% Mendeleev Communications 1 publication, 1.92%
Chinese Journal of Organic Chemistry	Chinese Journal of Organic Chemistry, 1, 1.92% Chinese Journal of Organic Chemistry 1 publication, 1.92%
	1 2 3 4 5 6 7

Publishers

	2 4 6 8 10 12 14
American Chemical Society (ACS)	American Chemical Society (ACS), 14, 26.92% American Chemical Society (ACS) 14 publications, 26.92%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 13, 25% Royal Society of Chemistry (RSC) 13 publications, 25%
Wiley	Wiley, 11, 21.15% Wiley 11 publications, 21.15%
Springer Nature	Springer Nature, 3, 5.77% Springer Nature 3 publications, 5.77%
Elsevier	Elsevier, 3, 5.77% Elsevier 3 publications, 5.77%
Georg Thieme Verlag KG	Georg Thieme Verlag KG, 3, 5.77% Georg Thieme Verlag KG 3 publications, 5.77%
Beilstein-Institut	Beilstein-Institut, 1, 1.92% Beilstein-Institut 1 publication, 1.92%
Frontiers Media S.A.	Frontiers Media S.A., 1, 1.92% Frontiers Media S.A. 1 publication, 1.92%
Science in China Press	Science in China Press, 1, 1.92% Science in China Press 1 publication, 1.92%
OOO Zhurnal "Mendeleevskie Soobshcheniya"	OOO Zhurnal "Mendeleevskie Soobshcheniya", 1, 1.92% OOO Zhurnal "Mendeleevskie Soobshcheniya" 1 publication, 1.92%
Shanghai Institute of Organic Chemistry	Shanghai Institute of Organic Chemistry, 1, 1.92% Shanghai Institute of Organic Chemistry 1 publication, 1.92%
	2 4 6 8 10 12 14

We do not take into account publications without a DOI.
Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.

Metrics

Cite this

GOST |

Cite this

GOST Copy

Meloche J. L., Ashfeld B. L. A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles // Angewandte Chemie - International Edition. 2017. Vol. 56. No. 23. pp. 6604-6608.

GOST all authors (up to 50) Copy

RIS |

Cite this

RIS Copy

TY - JOUR

DO - 10.1002/anie.201701147

UR - https://doi.org/10.1002/anie.201701147

TI - A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles

T2 - Angewandte Chemie - International Edition

AU - Meloche, Jennifer L

AU - Ashfeld, Brandon L

PY - 2017

DA - 2017/05/03

PB - Wiley

SP - 6604-6608

IS - 23

VL - 56

PMID - 28466963

SN - 1433-7851

SN - 1521-3773

ER -

BibTex |

Cite this

BibTex (up to 50 authors) Copy

@article{2017_Meloche,

author = {Jennifer L Meloche and Brandon L Ashfeld},

title = {A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles},

journal = {Angewandte Chemie - International Edition},

year = {2017},

volume = {56},

publisher = {Wiley},

month = {may},

url = {https://doi.org/10.1002/anie.201701147},

number = {23},

pages = {6604--6608},

doi = {10.1002/anie.201701147}

}

MLA

Cite this

MLA Copy

Meloche, Jennifer L., and Brandon L Ashfeld. “A Rhodium(II)‐Catalyzed Formal [4+1]‐Cycloaddition toward Spirooxindole Pyrrolone Construction Employing Vinyl Isocyanates as 1,4‐Dipoles.” Angewandte Chemie - International Edition, vol. 56, no. 23, May. 2017, pp. 6604-6608. https://doi.org/10.1002/anie.201701147.

Publisher

Wiley

Journal

Angewandte Chemie - International Edition

scimago Q1

wos Q1

SJR

5.550

CiteScore

27.6

Impact factor

16.9

ISSN

14337851 (Print)

15213773 (Electronic)