Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes

Maxime Giardinetti; Nicolaj Inunnguaq Jessen; Mette Louise Christensen; Karl Anker Jørgensen

doi:10.1039/C8CC08551J

Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes

Maxime Giardinetti, Nicolaj Inunnguaq Jessen, Mette Louise Christensen, Karl Anker Jørgensen^*

^*Corresponding author for this work

Department of Chemistry

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review

Abstract

A direct and mild strategy for the synthesis of benzo[a]azulenes based on an organocatalytic [10+4] cycloaddition reaction is described. The strategy enables a diversity-oriented approach for the synthesis of various poly-functionalised azulenes from easily accessible starting materials.

Original language	English
Journal	Chemical Communications
Volume	55
Issue	2
Pages (from-to)	202-205
Number of pages	4
ISSN	1359-7345
DOIs	https://doi.org/10.1039/C8CC08551J
Publication status	Published - 1 Jan 2019

Access to Document

10.1039/C8CC08551J

Cite this

@article{a73f2e57472e49409bee93cc367ad63c,

title = "Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes",

abstract = "A direct and mild strategy for the synthesis of benzo[a]azulenes based on an organocatalytic [10+4] cycloaddition reaction is described. The strategy enables a diversity-oriented approach for the synthesis of various poly-functionalised azulenes from easily accessible starting materials.",

author = "Maxime Giardinetti and Jessen, {Nicolaj Inunnguaq} and Christensen, {Mette Louise} and J{\o}rgensen, {Karl Anker}",

year = "2019",

month = jan,

day = "1",

doi = "10.1039/C8CC08551J",

language = "English",

volume = "55",

pages = "202--205",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "ROYAL SOC CHEMISTRY",

number = "2",

}

Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes. / Giardinetti, Maxime; Jessen, Nicolaj Inunnguaq; Christensen, Mette Louise et al.
In: Chemical Communications, Vol. 55, No. 2, 01.01.2019, p. 202-205.

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review

TY - JOUR

T1 - Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes

AU - Giardinetti, Maxime

AU - Jessen, Nicolaj Inunnguaq

AU - Christensen, Mette Louise

AU - Jørgensen, Karl Anker

PY - 2019/1/1

Y1 - 2019/1/1

N2 - A direct and mild strategy for the synthesis of benzo[a]azulenes based on an organocatalytic [10+4] cycloaddition reaction is described. The strategy enables a diversity-oriented approach for the synthesis of various poly-functionalised azulenes from easily accessible starting materials.

AB - A direct and mild strategy for the synthesis of benzo[a]azulenes based on an organocatalytic [10+4] cycloaddition reaction is described. The strategy enables a diversity-oriented approach for the synthesis of various poly-functionalised azulenes from easily accessible starting materials.

UR - http://www.scopus.com/inward/record.url?scp=85058892074&partnerID=8YFLogxK

U2 - 10.1039/C8CC08551J

DO - 10.1039/C8CC08551J

M3 - Journal article

C2 - 30520898

AN - SCOPUS:85058892074

SN - 1359-7345

VL - 55

SP - 202

EP - 205

JO - Chemical Communications

JF - Chemical Communications

IS - 2

ER -

Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[a]azulenes

Abstract

Access to Document

Other files and links

Fingerprint

Cite this