Synthesis of 2-oxophosphorindolines via the copper-catalyzed intramolecular aromatic C–H insertion of diazophosphonamidates-Reference-Cited by-同舟云学术

Synthesis of 2-oxophosphorindolines via the copper-catalyzed intramolecular aromatic C–H insertion of diazophosphonamidates

Published:2016 Issue:68 Volume:6 Page:63736-63748
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Huang Peipei¹²³⁴⁵,Xu Jiaxi¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Chemical Resource Engineering

2. Department of Organic Chemistry

3. Faculty of Science

4. Beijing University of Chemical Technology

5. Beijing 100029

Abstract

2-Ethoxy-2-oxophosphorindolines, benzo-γ-phospholactams, were synthesized efficiently with up to 97% yield through the copper-catalyzed intramolecular aromatic C–H insertion of diazophosphonamidates.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA10555F

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2. Organophosphorus Analogues and Derivatives of the Natural L-Amino Carboxylic Acids and Peptides. I. Enzymatic Synthesis of D-, DL-, and L-Phosphinothricin and Their Cyclic Analogues

3. Phosphaisocoumarins as a new class of potent inhibitors for pancreatic cholesterol esterase

4. P-Heterocycles as Ligands in Homogeneous Catalytic Reactions

5. Synthesis of diethyl N-dodecylphosphoramidate analogs as potential inhibitors of dental plaque

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