Exploiting the o-Quinodimethane Nature of Naphthalene: Cycloaddition Reactions with η2-Coordinated Tungsten–Naphthalene Complexes-Reference-Cited by-同舟云学术

Exploiting the o-Quinodimethane Nature of Naphthalene: Cycloaddition Reactions with η2-Coordinated Tungsten–Naphthalene Complexes

Published:2013-01-30 Issue:3 Volume:32 Page:915-925
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Strausberg Laura¹,Li Mengxun¹,Harrison Daniel P.¹,Myers William H.²,Sabat Michal³,Harman W. Dean¹

Affiliation:

1. Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States

2. Department of Chemistry, University of Richmond, Richmond, Virginia 27173, United States

3. Nanoscale Materials Characterization Facility, Department of Materials Science and Engineering, University of Virginia, Charlottesville, Virginia 22904, United States

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om301238q

Reference19 articles.

1. Total Synthesis of taxol. 2. Construction of A and C ring intermediates and initial attempts to construct the ABC ring system

2. Total Synthesis of Hamigerans and Analogues Thereof. Photochemical Generation and Diels−Alder Trapping of Hydroxy-o-quinodimethanes

3. o-Quinodimethanes: Efficient Intermediates in Organic Synthesis

4. Diels-Alder reactivity of polycyclic aromatic hydrocarbons. 1. Acenes and benzologs

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