Solid-State Structural Analysis of the “Naked” Isodicyclopentadienide Anion-Reference-Cited by-同舟云学术

Solid-State Structural Analysis of the “Naked” Isodicyclopentadienide Anion

Published:1998-01-01 Issue:1 Volume:17 Page:111-113
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Gallucci Judith C.¹,Gobley Olivier¹,Zaegel Florence¹,Meunier Philippe¹,Gautheron Bernard¹,Lange Holger¹,Gleiter Rolf¹,Kozmina Natasha¹,Paquette Leo A.¹

Affiliation:

1. Department of Chemistry, The Ohio State University, Columbus, Ohio 43210, Laboratoire de Synthèse et d'Electrosynthèse Organometalliques Associé au CNRS, UMR 5632, Université de Bourgogne, BP 138, 21004 Dijon CEDEX, France, and Organisch-Chemisches Institut der Universität Heidelberg, 69120 Heidelberg, Germany

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om970643w

Reference38 articles.

1. Über das Iso‐dicyclopentadien und das Dehydro‐iso‐dicyclopentadien

2. Syn selectivity in Diels-Alder reactions of isodicyclopentadiene

3. Electronic control of stereoselectivity. 3. Stereoselection operative in [4 + 2].pi. cycloadditions to cyclopentadiene rings fused at C2,C3 to bicyclic frameworks

4. Electronic control of stereoselectivity. 4. Effects of neighboring fused bicyclic frameworks on the stereochemical outcome of Diels-Alder cycloadditions to cyclopentadiene rings

5. Electronic control of stereoselectivity. 7. Stereospecificity of N-methyltriazolinedione cycloaddition to tricyclo[5.2.1.02,6]deca-2,5-diene, tricyclo[5.2.1.02,6]deca-2,5,8-triene, and tricyclo[5.2.2.02,6]undeca-2,5,8-triene

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