Control of Chemoselectivity of SET-Promoted Photoaddition Reactions of Fullerene C60 with α-Trimethylsilyl Group-Containing N-Alkylglycinates Yielding Aminomethyl-1,2-dihydrofullerenes or Fulleropyrrolidines-Reference-Cited by-同舟云学术

Control of Chemoselectivity of SET-Promoted Photoaddition Reactions of Fullerene C60 with α-Trimethylsilyl Group-Containing N-Alkylglycinates Yielding Aminomethyl-1,2-dihydrofullerenes or Fulleropyrrolidines

Published:2020-09-24 Issue:20 Volume:85 Page:12882-12900
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lim Suk Hyun¹,Ahn Mina²,Wee Kyung-Ryang²^ORCID,Shim Jun Ho²,Choi Jungkweon³^ORCID,Ahn Doo-Sik³,Cho Dae Won¹^ORCID

Affiliation:

1. Department of Chemistry, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Korea

2. Department of Chemistry and Institute of Basic Science, Daegu University, Gyeongsan, Gyeongbuk 38453, Korea

3. Center for Nanomaterials and Chemical Reactions, Institute for Basic Science (IBS), Daejeon 305-701, Korea

Funder

National Research Foundation of Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01324

Reference76 articles.

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4. Photochemical addition of tertiary amines to stilbene. Free-radical and electron-transfer mechanisms for amine oxidation

5. Single electron transfer promoted photocyclization reactions of (aminoalkyl)cyclohexenones. Mechanistic and synthetic features of processes involving the generation and reactions of amine cation and .alpha.-amino radicals

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