Novel synthesis of benzotriazolyl alkyl esters: an unprecedented CH2insertion

Mohamed Elagawany; Lingaiah Maram; Bahaa Elgendy

doi:10.1039/d0ra10413b

Novel synthesis of benzotriazolyl alkyl esters: an unprecedented CH₂insertion

Mohamed Elagawany
, Lingaiah Maram
, Bahaa Elgendy

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

We have developed a novel method for the synthesis of benzotriazolyl alkyl esters (BAEs) fromN-acylbenzotriazoles and dichloromethane (DCM) under mild conditions. This reaction is one of few examples to show the use of DCM as a C-1 surrogate in carbon-heteroatom bond formation and to highlight the versatility of using DCM as a methylene building block.

Original language	English
Pages (from-to)	7564-7569
Number of pages	6
Journal	RSC Advances
Volume	11
Issue number	13
DOIs	https://doi.org/10.1039/d0ra10413b
State	Published - Feb 17 2021

Access to Document

10.1039/d0ra10413b

Cite this

@article{4e8b25bf44e14938a6ba38d16768d139,

title = "Novel synthesis of benzotriazolyl alkyl esters: an unprecedented CH2insertion",

abstract = "We have developed a novel method for the synthesis of benzotriazolyl alkyl esters (BAEs) fromN-acylbenzotriazoles and dichloromethane (DCM) under mild conditions. This reaction is one of few examples to show the use of DCM as a C-1 surrogate in carbon-heteroatom bond formation and to highlight the versatility of using DCM as a methylene building block.",

author = "Mohamed Elagawany and Lingaiah Maram and Bahaa Elgendy",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2021.",

year = "2021",

month = feb,

day = "17",

doi = "10.1039/d0ra10413b",

language = "English",

volume = "11",

pages = "7564--7569",

journal = "RSC Advances",

issn = "2046-2069",

number = "13",

}

TY - JOUR

T1 - Novel synthesis of benzotriazolyl alkyl esters

T2 - an unprecedented CH2insertion

AU - Elagawany, Mohamed

AU - Maram, Lingaiah

AU - Elgendy, Bahaa

N1 - Publisher Copyright: © The Royal Society of Chemistry 2021.

PY - 2021/2/17

Y1 - 2021/2/17

N2 - We have developed a novel method for the synthesis of benzotriazolyl alkyl esters (BAEs) fromN-acylbenzotriazoles and dichloromethane (DCM) under mild conditions. This reaction is one of few examples to show the use of DCM as a C-1 surrogate in carbon-heteroatom bond formation and to highlight the versatility of using DCM as a methylene building block.

AB - We have developed a novel method for the synthesis of benzotriazolyl alkyl esters (BAEs) fromN-acylbenzotriazoles and dichloromethane (DCM) under mild conditions. This reaction is one of few examples to show the use of DCM as a C-1 surrogate in carbon-heteroatom bond formation and to highlight the versatility of using DCM as a methylene building block.

UR - https://www.scopus.com/pages/publications/85100931142

U2 - 10.1039/d0ra10413b

DO - 10.1039/d0ra10413b

M3 - Article

AN - SCOPUS:85100931142

SN - 2046-2069

VL - 11

SP - 7564

EP - 7569

JO - RSC Advances

JF - RSC Advances

IS - 13

ER -

Novel synthesis of benzotriazolyl alkyl esters: an unprecedented CH₂insertion

Abstract

Access to Document

Other files and links

Fingerprint

Cite this