Photoinduced, strain-promoted cycloadditions oftrans-cycloheptenones and azides-Reference-Cited by-同舟云学术

Photoinduced, strain-promoted cycloadditions oftrans-cycloheptenones and azides

Published:2020 Issue:20 Volume:22 Page:7023-7030
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Yang Hongzhi¹²³⁴⁵,Zeng Tianying¹²³⁴⁵,Xi Shuang¹²³⁴⁵,Hu Shengkun⁶³⁷⁵,Wu Yunfei¹²³⁴⁵,Tang Yefeng¹²³⁴⁵^ORCID

Affiliation:

1. School of Pharmaceutical Sciences

2. MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology

3. Tsinghua University

4. Beijing 100084

5. China

6. Department of Chemistry

7. Beijing

Abstract

Metal-free cycloadditions of cycloheptenones with azides have been developed, hinging on a photoisomerization/1,3-dipolar cycloaddition/aerobic oxidation reaction sequence.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/GC/D0GC02347G

Reference83 articles.

1. 1,3-Dipolar Cycloadditions. Past and Future

2. Kinetics and Mechanism of 1,3-Dipolr Cycloadditions

3. 1.3‐Dipolare Cycloadditionen, XXXII. Kinetik der Additionen organischer Azide an CC‐Mehrfachbindungen

4. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

5. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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