Preparation of Di-μ-chlorobis[π-1-chloro-1-aryl-2-(2′,2′-diarylvinyl)allyl]palladium(II) Complexes and a Novel Dehydrogenative Rearrangement of Arylvinylcyclopropenes for the Synthesis of 7H-Benzo[c]fluorene Derivatives-Reference-Cited by-同舟云学术

Preparation of Di-μ-chlorobis[π-1-chloro-1-aryl-2-(2′,2′-diarylvinyl)allyl]palladium(II) Complexes and a Novel Dehydrogenative Rearrangement of Arylvinylcyclopropenes for the Synthesis of 7H-Benzo[c]fluorene Derivatives

Published:2011-01-10 Issue:3 Volume:30 Page:627-632
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Zhu Zhi-Bin¹,Chen Kai¹,Wei Yin²,Shi Min¹²

Affiliation:

1. Laboratory for Advanced Materials and Institute of Fine Chemicals, School of Chemistry & Molecular Engineering, East China University of Science and Technology, 130 Mei-Long Road, Shanghai 200237, People's Republic of China

2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, Shanghai 200032, People's Republic of China.

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om1009846

Reference92 articles.

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3. bGoldschmidt, Z.InThe Chemistry of the Cyclopropyl Group;Rappoport, Z., Ed.Wiley:New York, 1995; Vol.2, p495.

4. Strain Energy of Small Ring Hydrocarbons. Influence of C−H Bond Dissociation Energies

5. Why Are Methylenecyclopropane and 1-Methylcylopropene More “Strained” than Methylcyclopropane?

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