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From the same journal

A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones

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A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones. / Cuthbertson, James D.; Godfrey, Andrew A.; Taylor, Richard J. K.

In: Synlett, No. 18, 11.2010, p. 2805-2807.

Research output: Contribution to journalArticlepeer-review

Harvard

Cuthbertson, JD, Godfrey, AA & Taylor, RJK 2010, 'A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones', Synlett, no. 18, pp. 2805-2807. https://doi.org/10.1055/s-0030-1258811

APA

Cuthbertson, J. D., Godfrey, A. A., & Taylor, R. J. K. (2010). A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones. Synlett, (18), 2805-2807. https://doi.org/10.1055/s-0030-1258811

Vancouver

Cuthbertson JD, Godfrey AA, Taylor RJK. A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones. Synlett. 2010 Nov;(18):2805-2807. https://doi.org/10.1055/s-0030-1258811

Author

Cuthbertson, James D. ; Godfrey, Andrew A. ; Taylor, Richard J. K. / A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones. In: Synlett. 2010 ; No. 18. pp. 2805-2807.

Bibtex - Download

@article{54135b367fdd4ab3a86b44cbaf128cba,
title = "A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones",
abstract = "An efficient one-pot amination/lactamisation sequence for the preparation of 2-azabicyclo[2.2.2]octanones from 6-carboalkoxycyclohex-2-enones and aqueous ammonia is described. Scope and limitation studies are reported for this tandem procedure and a range of bicyclic compounds have been prepared, two of which were characterised by X-ray crystallography.",
keywords = "amination, lactamisation, azabicyclo[2.2.2]octanones, bicyclic compounds, 6-carboalkoxycyclohex-2-enones",
author = "Cuthbertson, {James D.} and Godfrey, {Andrew A.} and Taylor, {Richard J. K.}",
year = "2010",
month = nov,
doi = "10.1055/s-0030-1258811",
language = "English",
pages = "2805--2807",
journal = "Synlett",
issn = "1437-2096",
publisher = "Georg Thieme Verlag",
number = "18",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - A Tandem Amination/Lactamisation Route to 2-Azabicyclo[2.2.2]octanones

AU - Cuthbertson, James D.

AU - Godfrey, Andrew A.

AU - Taylor, Richard J. K.

PY - 2010/11

Y1 - 2010/11

N2 - An efficient one-pot amination/lactamisation sequence for the preparation of 2-azabicyclo[2.2.2]octanones from 6-carboalkoxycyclohex-2-enones and aqueous ammonia is described. Scope and limitation studies are reported for this tandem procedure and a range of bicyclic compounds have been prepared, two of which were characterised by X-ray crystallography.

AB - An efficient one-pot amination/lactamisation sequence for the preparation of 2-azabicyclo[2.2.2]octanones from 6-carboalkoxycyclohex-2-enones and aqueous ammonia is described. Scope and limitation studies are reported for this tandem procedure and a range of bicyclic compounds have been prepared, two of which were characterised by X-ray crystallography.

KW - amination

KW - lactamisation

KW - azabicyclo[2.2.2]octanones

KW - bicyclic compounds

KW - 6-carboalkoxycyclohex-2-enones

UR - http://www.scopus.com/inward/record.url?scp=78149285464&partnerID=8YFLogxK

U2 - 10.1055/s-0030-1258811

DO - 10.1055/s-0030-1258811

M3 - Article

SP - 2805

EP - 2807

JO - Synlett

JF - Synlett

SN - 1437-2096

IS - 18

ER -