Transformation of masked benzyl alcohols to o-aminobenzaldehydes through C–H activation: a facile approach to quinazolines-Reference-Cited by-同舟云学术

Transformation of masked benzyl alcohols to o-aminobenzaldehydes through C–H activation: a facile approach to quinazolines

Published:2016 Issue:67 Volume:52 Page:10241-10244
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Chen Xiaolan¹²³⁴⁵,Han Jian¹²³⁴⁵,Zhu Yan¹²³⁴⁵,Yuan Chunchen¹²³⁴⁵,Zhang Jingyu⁶⁷⁸⁹⁵,Zhao Yingsheng¹²³⁴⁵

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science, Soochow University

4. Suzhou 215123

5. P. R. China

6. College of Physics

7. Optoelectronics and Energy & Collaborative Innovation Center of Suzhou Nano Science and Technology

8. Soochow University

9. Suzhou 215006

Abstract

A decorating strategy has been developed for the synthesis of important synthetic units from benzyl alcohols through C–H functionalization.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C6CC05560E

Reference66 articles.

1. Remote functionalization of C-H and C-C bonds by "naked" transition-metal ions (Cosi Fan Tutte)

2. Catalytic C−H/Olefin Coupling

3. Low-Valent Cobalt Catalysis: New Opportunities for C–H Functionalization

4. Recent Advances of Transition-Metal Catalyzed Radical Oxidative Cross-Couplings

5. The Combined C–H Functionalization/Cope Rearrangement: Discovery and Applications in Organic Synthesis

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