Redox-neutral cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters: Access to cyanoalkylated dihydrofurans

Jia Yu Zhang; Xin Hua Duan; Jun Cheng Yang; Li Na Guo

doi:10.1021/acs.joc.8b00271

Redox-neutral cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters: Access to cyanoalkylated dihydrofurans

Jia Yu Zhang
, Xin Hua Duan
, Jun Cheng Yang
, Li Na Guo

School of Chemistry

Xi'an Jiaotong University

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

59 Scopus citations

Abstract

Metal-catalyzed cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters has been developed under redox-neutral conditions. This protocol provided a straightforward approach to diverse cyanoalkylated 2,3-dihydrofurans via a tandem ring-opening/addition/cyclization process.

Original language	English
Pages (from-to)	4239-4249
Number of pages	11
Journal	Journal of Organic Chemistry
Volume	83
Issue number	7
DOIs	https://doi.org/10.1021/acs.joc.8b00271
State	Published - 6 Apr 2018

Access to Document

10.1021/acs.joc.8b00271

Cite this

@article{deda35635a0445fc85c636d820afea10,

title = "Redox-neutral cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters: Access to cyanoalkylated dihydrofurans",

abstract = "Metal-catalyzed cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters has been developed under redox-neutral conditions. This protocol provided a straightforward approach to diverse cyanoalkylated 2,3-dihydrofurans via a tandem ring-opening/addition/cyclization process.",

author = "Zhang, \{Jia Yu\} and Duan, \{Xin Hua\} and Yang, \{Jun Cheng\} and Guo, \{Li Na\}",

note = "Publisher Copyright: {\textcopyright} 2018 American Chemical Society.",

year = "2018",

month = apr,

day = "6",

doi = "10.1021/acs.joc.8b00271",

language = "英语",

volume = "83",

pages = "4239--4249",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "7",

}

TY - JOUR

T1 - Redox-neutral cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters

T2 - Access to cyanoalkylated dihydrofurans

AU - Zhang, Jia Yu

AU - Duan, Xin Hua

AU - Yang, Jun Cheng

AU - Guo, Li Na

PY - 2018/4/6

Y1 - 2018/4/6

N2 - Metal-catalyzed cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters has been developed under redox-neutral conditions. This protocol provided a straightforward approach to diverse cyanoalkylated 2,3-dihydrofurans via a tandem ring-opening/addition/cyclization process.

AB - Metal-catalyzed cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters has been developed under redox-neutral conditions. This protocol provided a straightforward approach to diverse cyanoalkylated 2,3-dihydrofurans via a tandem ring-opening/addition/cyclization process.

UR - https://www.scopus.com/pages/publications/85045096013

U2 - 10.1021/acs.joc.8b00271

DO - 10.1021/acs.joc.8b00271

M3 - 文章

C2 - 29557652

AN - SCOPUS:85045096013

SN - 0022-3263

VL - 83

SP - 4239

EP - 4249

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 7

ER -

Redox-neutral cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters: Access to cyanoalkylated dihydrofurans

Abstract

Access to Document

Other files and links

Fingerprint

Cite this