1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides

Koichi Mitsudo, Kazuki Yoshioka, Takayuki Hirata, Hiroki Mandai, Koji Midorikawa, Seiji Suga

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.

Original languageEnglish
Article numberst-2019-b0070-c
Pages (from-to)1209-1214
Number of pages6
JournalSynlett
Volume30
Issue number10
DOIs
Publication statusPublished - Jan 1 2019

Fingerprint

Cyanides
Iodides
Electrons
1,10-phenanthroline

Keywords

  • aryl cyanides
  • aryl iodides
  • cyanation
  • electrochemistry
  • organocatalysis

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides. / Mitsudo, Koichi; Yoshioka, Kazuki; Hirata, Takayuki; Mandai, Hiroki; Midorikawa, Koji; Suga, Seiji.

In: Synlett, Vol. 30, No. 10, st-2019-b0070-c, 01.01.2019, p. 1209-1214.

Research output: Contribution to journalArticle

Mitsudo, K, Yoshioka, K, Hirata, T, Mandai, H, Midorikawa, K & Suga, S 2019, '1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides', Synlett, vol. 30, no. 10, st-2019-b0070-c, pp. 1209-1214. https://doi.org/10.1055/s-0037-1611793
Mitsudo, Koichi ; Yoshioka, Kazuki ; Hirata, Takayuki ; Mandai, Hiroki ; Midorikawa, Koji ; Suga, Seiji. / 1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides. In: Synlett. 2019 ; Vol. 30, No. 10. pp. 1209-1214.
@article{6481fcad3a384cbd9fbfdca6e6accb78,
title = "1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides",
abstract = "A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.",
keywords = "aryl cyanides, aryl iodides, cyanation, electrochemistry, organocatalysis",
author = "Koichi Mitsudo and Kazuki Yoshioka and Takayuki Hirata and Hiroki Mandai and Koji Midorikawa and Seiji Suga",
year = "2019",
month = "1",
day = "1",
doi = "10.1055/s-0037-1611793",
language = "English",
volume = "30",
pages = "1209--1214",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "10",

}

TY - JOUR

T1 - 1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides

AU - Mitsudo, Koichi

AU - Yoshioka, Kazuki

AU - Hirata, Takayuki

AU - Mandai, Hiroki

AU - Midorikawa, Koji

AU - Suga, Seiji

PY - 2019/1/1

Y1 - 2019/1/1

N2 - A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.

AB - A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.

KW - aryl cyanides

KW - aryl iodides

KW - cyanation

KW - electrochemistry

KW - organocatalysis

UR - http://www.scopus.com/inward/record.url?scp=85066464315&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85066464315&partnerID=8YFLogxK

U2 - 10.1055/s-0037-1611793

DO - 10.1055/s-0037-1611793

M3 - Article

VL - 30

SP - 1209

EP - 1214

JO - Synlett

JF - Synlett

SN - 0936-5214

IS - 10

M1 - st-2019-b0070-c

ER -