Efficient Synthesis of β-Keto-α-hydroxy Secondary (Primary) Amides by Selective Aminocarbonylation of Vicinal Diketones Using Carbamoylsilane as an Amide Source-Reference-Cited by-同舟云学术

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Efficient Synthesis of β-Keto-α-hydroxy Secondary (Primary) Amides by Selective Aminocarbonylation of Vicinal Diketones Using Carbamoylsilane as an Amide Source

Published:2020 Issue:6 Volume:40 Page:1737
ISSN:0253-2786
Container-title:Chinese Journal of Organic Chemistry
language:en
Short-container-title:Chin. J. Org. Chem.

Author:

Zhang Pengpeng,Han Shenghua,Chen Jianxin

Publisher

Shanghai Institute of Organic Chemistry

Subject

Organic Chemistry

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. From intramolecular cyclization to intermolecular hydrolysis: TMSCF₂Br-enabled carbonylation of aldehydes/ketones and amines to α-hydroxyamides;Organic Chemistry Frontiers;2023

2. E-Stereospecific 1,1-Carboboration of Terminal Arylalkynes with [IB(C₆F₅)₃]^–;Chinese Journal of Organic Chemistry;2023

3. Passerini Reaction to Access α‐Hydroxy Amides by Facile Decarbonylation/Decarboxylation of Oxalic Acid;European Journal of Organic Chemistry;2022-12-20

4. Synthesis of ?-Nitroamide Derivatives Based on Carbamoylsilane;CHINESE J ORG CHEM;2022

5. Efficient synthesis of β-nitro amides by aminocarbonylation of ethoxycarbonyl-containing nitroalkenes with carbamoylsilane;Mendeleev Communications;2021-01

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