Tandem Phospha‐Michael Addition/ N ‐Acylation/ Intramolecular Wittig Reaction of aza‐ o ‐Quinone Methides: Approaches to 2,3‐Disubstituted Indoles-Reference-Cited by-同舟云学术

Tandem Phospha‐Michael Addition/ N ‐Acylation/ Intramolecular Wittig Reaction of aza‐ o ‐Quinone Methides: Approaches to 2,3‐Disubstituted Indoles

Published:2020-05-11 Issue:13 Volume:362 Page:2615-2619
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Hua Ting‐Bi¹²,Chao Fei¹,Wang Long¹,Yan Chen‐Yang¹,Xiao Cong³,Yang Qing‐Qing¹²,Xiao Wen‐Jing⁴

Affiliation:

1. College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion MaterialsChina Three Gorges University 8 Daxue Road Yichang, Hubei 443002 People's Republic of China

2. Hubei Key Laboratory of Natural Products Research and DevelopmentChina Three Gorges University 8 Daxue Road Yichang, Hubei 443002 People's Republic of China

3. Wuhan Glycolipid Co. Ltd. NO.666, East Lake High-tech Development Zone Wuhan, Hubei 430075 People's Republic of China

4. Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of ChemistryCentral China Normal University 152 Luoyu Road Wuhan, Hubei 430079 People's Republic of China.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202000343

Reference87 articles.

2. Aza-ortho-xylylenes in Organic Synthesis

3. Quinone Methides

4. Emerging Roles of in Situ Generated Quinone Methides in Metal-Free Catalysis

5. Stereoselective Reactions of ortho-Quinone Methide and ortho-Quinone Methide Imines and Their Utility in Natural Product Synthesis

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