4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate. / Christensen, Jørn Bolstad; Sørensen, Jeanett N.; Schaumburg, Kjeld; Bechgaard, Klaus.

In: Molbank, Vol. 2014, No. 1, M812, 2014.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Christensen, JB, Sørensen, JN, Schaumburg, K & Bechgaard, K 2014, '4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate', Molbank, vol. 2014, no. 1, M812. https://doi.org/10.3390/M812

APA

Christensen, J. B., Sørensen, J. N., Schaumburg, K., & Bechgaard, K. (2014). 4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate. Molbank, 2014(1), [M812]. https://doi.org/10.3390/M812

Vancouver

Christensen JB, Sørensen JN, Schaumburg K, Bechgaard K. 4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate. Molbank. 2014;2014(1). M812. https://doi.org/10.3390/M812

Author

Christensen, Jørn Bolstad ; Sørensen, Jeanett N. ; Schaumburg, Kjeld ; Bechgaard, Klaus. / 4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate. In: Molbank. 2014 ; Vol. 2014, No. 1.

Bibtex

@article{10db08d554e743508631a543c9b07bdc,
title = "4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate",
abstract = "4,8-Diallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate (1) which is a highly substituted naphthalene derivative has been synthesized in two steps starting from 2,6-dimethyl-1,5-naphthalenediol (3) using a modified Claisen-rearrangement.",
keywords = "1,2,4,5,6,8-hexasubstituted naphthalene, Claisen-rearrangement",
author = "Christensen, {J{\o}rn Bolstad} and S{\o}rensen, {Jeanett N.} and Kjeld Schaumburg and Klaus Bechgaard",
note = "OA",
year = "2014",
doi = "10.3390/M812",
language = "English",
volume = "2014",
journal = "MolBank",
issn = "1422-8599",
publisher = "M D P I AG",
number = "1",

}

RIS

TY - JOUR

T1 - 4,8-bisallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate

AU - Christensen, Jørn Bolstad

AU - Sørensen, Jeanett N.

AU - Schaumburg, Kjeld

AU - Bechgaard, Klaus

N1 - OA

PY - 2014

Y1 - 2014

N2 - 4,8-Diallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate (1) which is a highly substituted naphthalene derivative has been synthesized in two steps starting from 2,6-dimethyl-1,5-naphthalenediol (3) using a modified Claisen-rearrangement.

AB - 4,8-Diallyl-2,6-dimethylnaphthalene-1,5-diyl diacetate (1) which is a highly substituted naphthalene derivative has been synthesized in two steps starting from 2,6-dimethyl-1,5-naphthalenediol (3) using a modified Claisen-rearrangement.

KW - 1,2,4,5,6,8-hexasubstituted naphthalene

KW - Claisen-rearrangement

U2 - 10.3390/M812

DO - 10.3390/M812

M3 - Journal article

AN - SCOPUS:84892562630

VL - 2014

JO - MolBank

JF - MolBank

SN - 1422-8599

IS - 1

M1 - M812

ER -

ID: 130987110