Photochemically-induced C–C bond formation between tertiary amines and nitrones-Reference-Cited by-同舟云学术

Photochemically-induced C–C bond formation between tertiary amines and nitrones

Published:2015 Issue:33 Volume:13 Page:8919-8924
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Itoh Kennosuke¹²³⁴⁵,Kato Ryo⁶⁷⁸⁵,Kinugawa Daito⁶⁷⁸⁵,Kamiya Hideaki⁶⁷⁸⁵,Kudo Ryuki¹²³⁴⁵,Hasegawa Masayuki⁹¹⁰¹¹¹²¹³,Fujii Hideaki¹²³⁴⁵,Suga Hiroyuki⁶⁷⁸⁵

Affiliation:

1. Department of Medicinal Chemistry

2. School of Pharmacy

3. Kitasato University

4. Tokyo 108-8641

5. Japan

6. Department of Chemistry and Material Engineering

7. Shinshu University

8. Nagano 380-8553

9. Planning & Coordination Office

10. Petrochemicals & Plastics Sector

11. Sumitomo Chemical Co.

12. Ltd.

13. Tokyo 104-8260

Abstract

Photoexcited nitrones serve as excellent electron acceptors as well as radical acceptors in the presence of tertiary amines to give β-amino hydroxylamines via photochemically-induced direct sp³ C–H functionalization of the tertiary amines.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01277E

Reference61 articles.

1. Asymmetric photochemistry in solution

2. Asymmetric photochemical reactions in solution

3. Photochemical Reactions as Key Steps in Organic Synthesis

4. Photochemical Reactions as Key Steps in Natural Product Synthesis

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