Remote Functionalization of C60 with Enantiomerically Pure cyclo-[2]-Malonate Tethers Bearing C12 and C14 Spacers: Synthetic Access to Bisadducts of C60 with the Inherently Chiral trans-3 Addition Pattern-Reference-Cited by-同舟云学术

Remote Functionalization of C60 with Enantiomerically Pure cyclo-[2]-Malonate Tethers Bearing C12 and C14 Spacers: Synthetic Access to Bisadducts of C60 with the Inherently Chiral trans-3 Addition Pattern

Published:2013-07-17 Issue:15 Volume:78 Page:7701-7713
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Riala Maria¹,Chronakis Nikos¹

Affiliation:

1. Department of Chemistry, University of Cyprus, University Str 1, Building no. 13, Aglantzia, 2109 Nicosia, Cyprus

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo4013173

Reference58 articles.

1. Principles of Fullerene Reactivity

2. Fullerene Chemistry in Three Dimensions: Isolation of Seven Regioisomeric Bisadducts and Chiral Trisadducts of C60 and Di(ethoxycarbonyl)methylene

3. Structural Aspects of Fullerene ChemistryA Journey through Fullerene Chirality

4. Regioselectivity of Multiple Cyclopropanations of C60 and Introduction of a General Bond-Labeling Algorithm for Fullerenes and Their Derivatives

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