Orienting Effect of the Cage Addends: The Case of Nucleophilic Cyclopropanation ofC2-C70(CF3)8-Reference-Cited by-同舟云学术

Orienting Effect of the Cage Addends: The Case of Nucleophilic Cyclopropanation ofC2-C70(CF3)8

Published:2015-03-30 Issue:6 Volume:10 Page:1370-1378
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Apenova Marina G.¹,Semivrazhskaya Olesya O.¹,Borkovskaya Eugenia V.¹,Belov Nikita M.¹,Ioffe Ilya N.¹,Markov Vitaliy Yu.¹,Troyanov Sergey I.¹,Lukonina Natalia S.¹,Sidorov Lev N.¹,Goryunkov Alexey A.¹

Affiliation:

1. Chemistry Department; M. V. Lomonosov Moscow State University; Leninskie Gory, 1-3 119991 Moscow Russia

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/asia.201500079/fullpdf

Reference51 articles.

1. Synthesis, Characterization, and Theoretical Study of Stable Isomers of C70(CF3)n (n = 2, 4, 6, 8, 10)

2. Structure of 1,4,10,19,25,41-C70(CF3)6, isomer with unique arrangement of addends

3. Preparation, crystallographic characterization and theoretical study of two isomers of C70(CF3)12

4. Isolation and structural characterization of the most highly trifluoromethylated C70fullerenes: C70(CF3)18and C70(CF3)20

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4. Regioselective Synthesis of [6,6]-Open and [5,6]-Closed C70 (CF3 )8 [CH2 ] Methanofullerenes with Rapid [6,6]-to-[5,6] Phototransformation;European Journal of Organic Chemistry;2018-01-30

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