Chemical Communications, volume 49, issue 88, pages 10406-10408

Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters

Rubén Tejero ¹

Alberto Ponce ¹

Javier Adrio ¹

Juan Manuel Carretero ¹

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Departamento de Química Orgánica, Facultad de Ciencias, Universidad Autónoma de Madrid, Cantoblanco 28049, Madrid, Spain |

Publication type: Journal Article

Publication date: 2013-09-17

Royal Society of Chemistry (RSC)

Journal: Chemical Communications

Quartile SCImago

Quartile WOS

Impact factor: 4.9

ISSN: 13597345, 1364548X

DOI: 10.1039/c3cc45552a

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Materials Chemistry

Metals and Alloys

Surfaces, Coatings and Films

General Chemistry

Ceramics and Composites

Electronic, Optical and Magnetic Materials

Catalysis

Abstract

Synthesis of cycloheptapyrane derivatives was accomplished via Ni(ClO₄)₂·6H₂O catalyzed [8+3] cycloaddition of tropone with donor–acceptor cyclopropanes. The enantioselective variant of the process was achieved using either an enantiopure substituted cyclopropane or the combination of a racemic cyclopropane and a suitable chiral Lewis acid.

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Angewandte Chemie	Angewandte Chemie, 9, 13.04% Angewandte Chemie 9 publications, 13.04%
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Journal of the American Chemical Society	Journal of the American Chemical Society, 3, 4.35% Journal of the American Chemical Society 3 publications, 4.35%
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Chinese Journal of Organic Chemistry	Chinese Journal of Organic Chemistry, 1, 1.45% Chinese Journal of Organic Chemistry 1 publication, 1.45%
Nature Chemistry	Nature Chemistry, 1, 1.45% Nature Chemistry 1 publication, 1.45%
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Advanced Synthesis and Catalysis	Advanced Synthesis and Catalysis, 1, 1.45% Advanced Synthesis and Catalysis 1 publication, 1.45%
Chemical Record	Chemical Record, 1, 1.45% Chemical Record 1 publication, 1.45%
Chinese Journal of Chemistry	Chinese Journal of Chemistry, 1, 1.45% Chinese Journal of Chemistry 1 publication, 1.45%
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ACS Catalysis	ACS Catalysis, 1, 1.45% ACS Catalysis 1 publication, 1.45%
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Dalton Transactions	Dalton Transactions, 1, 1.45% Dalton Transactions 1 publication, 1.45%
Progress in Heterocyclic Chemistry	Progress in Heterocyclic Chemistry, 1, 1.45% Progress in Heterocyclic Chemistry 1 publication, 1.45%
ACS Omega	ACS Omega, 1, 1.45% ACS Omega 1 publication, 1.45%
Synlett	Synlett, 1, 1.45% Synlett 1 publication, 1.45%
Journal of Organometallic Chemistry	Journal of Organometallic Chemistry, 1, 1.45% Journal of Organometallic Chemistry 1 publication, 1.45%
Russian Chemical Bulletin	Russian Chemical Bulletin, 1, 1.45% Russian Chemical Bulletin 1 publication, 1.45%
	1 2 3 4 5 6 7 8 9

Citations by publishers

	5 10 15 20 25 30
Wiley	Wiley, 30, 43.48% Wiley 30 publications, 43.48%
American Chemical Society (ACS)	American Chemical Society (ACS), 17, 24.64% American Chemical Society (ACS) 17 publications, 24.64%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 8, 11.59% Royal Society of Chemistry (RSC) 8 publications, 11.59%
Elsevier	Elsevier, 5, 7.25% Elsevier 5 publications, 7.25%
Thieme	Thieme, 3, 4.35% Thieme 3 publications, 4.35%
Springer Nature	Springer Nature, 2, 2.9% Springer Nature 2 publications, 2.9%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 2, 2.9% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 2 publications, 2.9%
Shanghai Institute of Organic Chemistry	Shanghai Institute of Organic Chemistry, 1, 1.45% Shanghai Institute of Organic Chemistry 1 publication, 1.45%
	5 10 15 20 25 30

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Tejero R. et al. Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters // Chemical Communications. 2013. Vol. 49. No. 88. pp. 10406-10408.

GOST all authors (up to 50) Copy

Tejero R., Ponce A., Adrio J., Carretero J. M. Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters // Chemical Communications. 2013. Vol. 49. No. 88. pp. 10406-10408.

RIS |

Cite this

RIS Copy

TY - JOUR

DO - 10.1039/c3cc45552a

UR - https://doi.org/10.1039/c3cc45552a

TI - Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters

T2 - Chemical Communications

AU - Adrio, Javier

AU - Carretero, Juan Manuel

AU - Tejero, Rubén

AU - Ponce, Alberto

PY - 2013

DA - 2013/09/17 00:00:00

PB - Royal Society of Chemistry (RSC)

SP - 10406-10408

IS - 88

VL - 49

SN - 1359-7345

SN - 1364-548X

ER -

BibTex |

Cite this

BibTex Copy

@article{2013_Tejero,

author = {Javier Adrio and Juan Manuel Carretero and Rubén Tejero and Alberto Ponce},

title = {Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters},

journal = {Chemical Communications},

year = {2013},

volume = {49},

publisher = {Royal Society of Chemistry (RSC)},

month = {sep},

url = {https://doi.org/10.1039/c3cc45552a},

number = {88},

pages = {10406--10408},

doi = {10.1039/c3cc45552a}

}

MLA

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MLA Copy

Tejero, Rubén, et al. “Ni-Catalyzed [8+3] cycloaddition of tropones with 1,1-cyclopropanediesters.” Chemical Communications, vol. 49, no. 88, Sep. 2013, pp. 10406-10408. https://doi.org/10.1039/c3cc45552a.

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Publisher

Royal Society of Chemistry (RSC)

Journal

Chemical Communications

Quartile SCImago

Quartile WOS

Impact factor

4.9

ISSN

13597345 (Print)
1364548X (Electronic)