A rare γ-pyranopyrazole skeleton: Design, one-pot synthesis and computational study

Muhammed Üçüncü; Ceren Cantürk; Erman Karakuş; Hüseyin Zeybek; Uǧur Bozkaya; Emine Soydaş; Ertan Şahin; Mustafa Emrullahoǧlu

doi:10.1039/c6ob01099g

A rare γ-pyranopyrazole skeleton: Design, one-pot synthesis and computational study

Muhammed Üçüncü
, Ceren Cantürk
, Erman Karakuş
, Hüseyin Zeybek
, Uǧur Bozkaya
, Emine Soydaş
, Ertan Şahin
, Mustafa Emrullahoǧlu

Division of Theoretical Chemistry

Izmir Institute of Technology
Ataturk University

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

7 Citations (Scopus)

Abstract

Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies.

Original language	English
Pages (from-to)	7490-7494
Number of pages	5
Journal	Organic and Biomolecular Chemistry
Volume	14
Issue number	31
DOIs	https://doi.org/10.1039/c6ob01099g
Publication status	Published - 2016

Access to Document

10.1039/c6ob01099g

Cite this

@article{47e41949992a4ec1b474a086641b6d98,

title = "A rare γ-pyranopyrazole skeleton: Design, one-pot synthesis and computational study",

abstract = "Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies.",

author = "Muhammed {\"U}{\c c}{\"u}nc{\"u} and Ceren Cant{\"u}rk and Erman Karaku{\c s} and H{\"u}seyin Zeybek and Uǧur Bozkaya and Emine Soyda{\c s} and Ertan {\c S}ahin and Mustafa Emrullahoǧlu",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2016.",

year = "2016",

doi = "10.1039/c6ob01099g",

language = "English",

volume = "14",

pages = "7490--7494",

journal = "Organic and Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "31",

}

TY - JOUR

T1 - A rare γ-pyranopyrazole skeleton

T2 - Design, one-pot synthesis and computational study

AU - Üçüncü, Muhammed

AU - Cantürk, Ceren

AU - Karakuş, Erman

AU - Zeybek, Hüseyin

AU - Bozkaya, Uǧur

AU - Soydaş, Emine

AU - Şahin, Ertan

AU - Emrullahoǧlu, Mustafa

PY - 2016

Y1 - 2016

N2 - Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies.

AB - Drawing upon a consecutive amide coupling and intramolecular cyclisation pathway, a one-pot, straightforward synthetic route has been developed for a range of pyrazole fused γ-pyrone derivatives. The reaction mechanism proposed for the chemoselective formation of γ-pyranopyrazole is furthermore fully supported by experimental and computational studies.

UR - https://www.scopus.com/pages/publications/84981237569

U2 - 10.1039/c6ob01099g

DO - 10.1039/c6ob01099g

M3 - Article

AN - SCOPUS:84981237569

SN - 1477-0520

VL - 14

SP - 7490

EP - 7494

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 31

ER -

A rare γ-pyranopyrazole skeleton: Design, one-pot synthesis and computational study

Abstract

Access to Document

Other files and links

Fingerprint

Cite this