Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ-Reference-Cited by-同舟云学术

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Cross dehydrogenative coupling strategy for allylation of benzylanilines promoted by DDQ

Published:2020-01 Issue:1 Volume:76 Page:130798
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Xiong Ruimei,Hussain Muhammad Ijaz,Liu Qing,Xia Wen,Xiong Yan

Funder

National Natural Science Foundation of China

Natural Science Foundation Project of CQ CSTC

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. Efficient, divergent synthesis of cryptophycin unit A analogues

2. Asymmetric Petasis Borono‐Mannich Allylation Reactions Catalyzed by Chiral Biphenols

3. Synthesis of 1-Aza-cryptophycin 1, an Unstable Cryptophycin. An Unusual Skeletal Rearrangement

4. Recent developments in asymmetric catalytic addition to CN bonds

5. Eponemycin analogues: syntheses and use as probes of angiogenesis

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1. Lewis Acid‐Promoted Domino Processes for the Synthesis of Homoallylic Amines, Quinolines and Tetrahydroquinolines;Advanced Synthesis & Catalysis;2024-07

2. DDQ catalyzed oxidative lactonization of indole-3-butyric acids;RSC Advances;2024

3. Stereoselective Synthesis of Benzo[a]quinolizidines via Aerobic DDQ-Catalyzed Allylation and Reductive Cyclization;ACS Omega;2022-08-31

4. Synthesis of β-hydroxy-α-amino acid derivatives by the cross-dehydrogenative coupling of N-arylglycine esters with α-hydroxy ketones;Tetrahedron;2021-11

5. Tin powder‐promoted oxidation/allylation of glycine esters: Synthesis of γ , δ ‐unsaturated α ‐amino acid esters;Applied Organometallic Chemistry;2021-10-18

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