Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues

H. Jansen; J.C. Slootweg; K. Lammertsma

doi:10.3762/bjoc.7.201

Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues

H. Jansen, J.C. Slootweg, K. Lammertsma

Research output: Contribution to Journal › Article › Academic › peer-review

136 Downloads (Pure)

Abstract

The valence isomerization of the all-carbon and heteroelement analogues of cyclohepta-1,3,5-triene into the corresponding bicyclo[4.1.0]hepta-2,4-dienes is reviewed to show the impact of the heteroatom on the stability of both valence isomers. The focus is on the parent systems and their synthetic applications. © 2011 Jansen et al; licensee Beilstein-Institut.

Original language	English
Pages (from-to)	1713-1721
Journal	Beilstein Journal of Organic Chemistry
Volume	7
DOIs	https://doi.org/10.3762/bjoc.7.201
Publication status	Published - 2011

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.3762/bjoc.7.201

277079Final published version, 297 KB

Persistent URL (handle)

Copy link address

Cite this

@article{cd6157c501ed493eb7d9721252cd4911,

title = "Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues",

abstract = "The valence isomerization of the all-carbon and heteroelement analogues of cyclohepta-1,3,5-triene into the corresponding bicyclo[4.1.0]hepta-2,4-dienes is reviewed to show the impact of the heteroatom on the stability of both valence isomers. The focus is on the parent systems and their synthetic applications. {\textcopyright} 2011 Jansen et al; licensee Beilstein-Institut.",

author = "H. Jansen and J.C. Slootweg and K. Lammertsma",

year = "2011",

doi = "10.3762/bjoc.7.201",

language = "English",

volume = "7",

pages = "1713--1721",

journal = "Beilstein Journal of Organic Chemistry",

issn = "1860-5397",

publisher = "Beilstein-Institut Zur Forderung der Chemischen Wissenschaften",

}

TY - JOUR

T1 - Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues

AU - Jansen, H.

AU - Slootweg, J.C.

AU - Lammertsma, K.

PY - 2011

Y1 - 2011

N2 - The valence isomerization of the all-carbon and heteroelement analogues of cyclohepta-1,3,5-triene into the corresponding bicyclo[4.1.0]hepta-2,4-dienes is reviewed to show the impact of the heteroatom on the stability of both valence isomers. The focus is on the parent systems and their synthetic applications. © 2011 Jansen et al; licensee Beilstein-Institut.

AB - The valence isomerization of the all-carbon and heteroelement analogues of cyclohepta-1,3,5-triene into the corresponding bicyclo[4.1.0]hepta-2,4-dienes is reviewed to show the impact of the heteroatom on the stability of both valence isomers. The focus is on the parent systems and their synthetic applications. © 2011 Jansen et al; licensee Beilstein-Institut.

U2 - 10.3762/bjoc.7.201

DO - 10.3762/bjoc.7.201

M3 - Article

SN - 1860-5397

VL - 7

SP - 1713

EP - 1721

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

ER -

Valence isomerization of cyclohepta-1,3,5-triene and its heteroelement analogues

Abstract

UN SDGs

Access to Document

Persistent URL (handle)

Fingerprint

Cite this