THE TRAPPING OF 6,6-DIMETHYLISOBENZOFULVENE BY ITS 1,3-DIPOLAR PRECURSOR: A RARE EXAMPLE OF A DIPOLAR [6+4] CYCLOADDITION-Reference-Cited by-同舟云学术

THE TRAPPING OF 6,6-DIMETHYLISOBENZOFULVENE BY ITS 1,3-DIPOLAR PRECURSOR: A RARE EXAMPLE OF A DIPOLAR [6+4] CYCLOADDITION

Published:2001-01-01 Issue:8 Volume:31 Page:1167-1175
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Warrener Ronald N.¹,Hammond Malcom L. A.¹,Butler Douglas N.¹

Affiliation:

1. a Centre for Molecular Architecture, Central Queensland University , Rockhampton, Queensland, 4702, Australia

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-100104000

Reference25 articles.

1. Isobenzofulvenes. I. The in situ preparation of 8,8-Dimethyl- and 8,8-Diphenylbenzo[b]fulveues and their pericyclic reactions with 2π-Cycloaddends

2. Generation and Cycloaddition of 8,8-Dimethylisobenzofulvene

3. Gell , K. I. and Warrener , R. N. unpublished results

4. The preparation of 7-methylenebenzonorbornadiene, and its use in the synthesis of isobenzofolvene: coping with little fragmentation!

5. Warrener , R. N. Harrison , P. A. and Russell , R. A. 1998. Electronic Conference on Heterocyclic Chemistry '98. 1998. Edited by: Rzepa , H. S. and Kappe , O. pp.081Imperial College Press. http://www.ch.ic.ac.uk/ectoc/echet98/pub/081/index.htm

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