Synthesis 2017; 49(16): 3511-3534
DOI: 10.1055/s-0036-1588481
review
© Georg Thieme Verlag Stuttgart · New York

Recent Advances in Reactions of Heteroatom-Centered Radicals

School of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan   eMail: tsuyoshi@p.kanazawa-u.ac.jp
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This work was supported by MEXT/JSPS KAKENHI Grant-in-Aid for Scientific Research (C) (Grant No. 16K08159).
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Publikationsverlauf

Received: 27. Februar 2017

Accepted after revision: 05. April 2017

Publikationsdatum:
26. Juli 2017 (online)


Abstract

Heteroatom-centered radicals show versatile reactivity and offer useful synthetic methods in organic chemistry. The development of new approaches for forming heteroatom-centered radicals has recently expanded the practicality of radical chemistry for synthesis. This review focuses on recent advances in reactions of representative heteroatom-centered radicals.

1 Introduction

2 Group 17 Elements: Chlorine and Bromine Radicals

3 Group 15 and Group 16 Elements

3.1 Nitrogen- and Oxygen-Centered Radicals

3.2 Phosphorus- and Sulfur-Centered Radicals

3.3 Other Radicals

4 Group 14 Elements: Silicon-Centered Radicals

5 Group 13 Elements: Boron-Centered Radicals

6 Conclusion