Redox-Neutral C1 Functionalization of Unprotected Tetrahydroisoquinolines with Diazo Carbonyl Compounds-Reference-Cited by-同舟云学术

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Redox-Neutral C1 Functionalization of Unprotected Tetrahydroisoquinolines with Diazo Carbonyl Compounds

Published:2016-08-24 Issue:10 Volume:5 Page:1204-1207
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Huang Jun¹,Li Linyong¹,Xiao Tiebo¹,Mao Zong-wan¹,Zhou Lei¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering; Sun Yat-Sen University; 135 Xingang West Road Guangzhou 510275 China

Funder

National Program on Key Research Project

National Natural Science Foundation

Natural Science Funds of Guangdong Province for Distinguished Young Scholar

Publisher

Wiley

Subject

Organic Chemistry

Reference69 articles.

1. Modern Organic Synthesis with α-Diazocarbonyl Compounds

2. Recent studies on the reactions of α-diazocarbonyl compounds

3. Organic Synthesis with .alpha.-Diazo Carbonyl Compounds

4. A New Reactivity Mode for the Diazo Group: Diastereoselective 1,3-Aminoalkylation Reaction of β-Amino-α-Diazoesters To Give Triazolines

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1. Iminium and azonium-activated metal and oxidant-free C–H functionalization of aliphatic amines;Chemical Communications;2023

2. Divergent transformation of C,N-cyclic-N′-acyl azomethine imines by reaction with diazo compounds;Organic & Biomolecular Chemistry;2023

3. C–H Functionalization as an Imperative Tool Toward Multicomponent Synthesis and Modification of Heterocycles;Multicomponent Reactions towards Heterocycles;2021-11-26

4. Multicomponent Reactions Involving Diazo Reagents: A 5-Year Update;Molecules;2021-10-29

5. Condensation-Based Methods for the C–H Bond Functionalization of Amines;Synthesis;2021-09-02

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