The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]: Scope and Limitations of an Acid Catalyzed Ring-closing Reaction

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Standard

The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2] : Scope and Limitations of an Acid Catalyzed Ring-closing Reaction. / Christensen, Jørn B.; Bechgaard, Klaus.

I: Journal of Heterocyclic Chemistry, Bind 40, Nr. 5, 01.01.2003, s. 757-761.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Christensen, JB & Bechgaard, K 2003, 'The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]: Scope and Limitations of an Acid Catalyzed Ring-closing Reaction', Journal of Heterocyclic Chemistry, bind 40, nr. 5, s. 757-761. https://doi.org/10.1002/jhet.5570400503

APA

Christensen, J. B., & Bechgaard, K. (2003). The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]: Scope and Limitations of an Acid Catalyzed Ring-closing Reaction. Journal of Heterocyclic Chemistry, 40(5), 757-761. https://doi.org/10.1002/jhet.5570400503

Vancouver

Christensen JB, Bechgaard K. The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]: Scope and Limitations of an Acid Catalyzed Ring-closing Reaction. Journal of Heterocyclic Chemistry. 2003 jan. 1;40(5):757-761. https://doi.org/10.1002/jhet.5570400503

Author

Christensen, Jørn B. ; Bechgaard, Klaus. / The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2] : Scope and Limitations of an Acid Catalyzed Ring-closing Reaction. I: Journal of Heterocyclic Chemistry. 2003 ; Bind 40, Nr. 5. s. 757-761.

Bibtex

@article{0e2a461be05447d4b379adef8ea610be,
title = "The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]: Scope and Limitations of an Acid Catalyzed Ring-closing Reaction",
abstract = "One of the few methods for synthesis of 1,6-dioxapyrenes is the acid catalyzed cyclization of 2,6-disubstituted 1,5-bis(2-oxoalkoxy)naphthalenes. The scope and limitations of this reaction has been investigated and 11 new 2,7-disubstituted 1,6-dioxapyrenes have been prepared and characterized. Most of the compounds undergo two reversible oxidations to give the corresponding radical as well as di- cations.",
author = "Christensen, {J{\o}rn B.} and Klaus Bechgaard",
year = "2003",
month = jan,
day = "1",
doi = "10.1002/jhet.5570400503",
language = "English",
volume = "40",
pages = "757--761",
journal = "Journal of Heterocyclic Chemistry",
issn = "0022-152X",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - The Chemistry of 1,6-Dioxapyrenes Part 3 [1,2]

T2 - Scope and Limitations of an Acid Catalyzed Ring-closing Reaction

AU - Christensen, Jørn B.

AU - Bechgaard, Klaus

PY - 2003/1/1

Y1 - 2003/1/1

N2 - One of the few methods for synthesis of 1,6-dioxapyrenes is the acid catalyzed cyclization of 2,6-disubstituted 1,5-bis(2-oxoalkoxy)naphthalenes. The scope and limitations of this reaction has been investigated and 11 new 2,7-disubstituted 1,6-dioxapyrenes have been prepared and characterized. Most of the compounds undergo two reversible oxidations to give the corresponding radical as well as di- cations.

AB - One of the few methods for synthesis of 1,6-dioxapyrenes is the acid catalyzed cyclization of 2,6-disubstituted 1,5-bis(2-oxoalkoxy)naphthalenes. The scope and limitations of this reaction has been investigated and 11 new 2,7-disubstituted 1,6-dioxapyrenes have been prepared and characterized. Most of the compounds undergo two reversible oxidations to give the corresponding radical as well as di- cations.

UR - http://www.scopus.com/inward/record.url?scp=0242267049&partnerID=8YFLogxK

U2 - 10.1002/jhet.5570400503

DO - 10.1002/jhet.5570400503

M3 - Journal article

AN - SCOPUS:0242267049

VL - 40

SP - 757

EP - 761

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

SN - 0022-152X

IS - 5

ER -

ID: 241879633