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Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway

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Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway. / Murphy, P.J.; Evans, D.M.; Horton, P.N. et al.
In: RSC Advances, Vol. 4, No. 40, 28.04.2014, p. 20744-20751.

Research output: Contribution to journal › Article › peer-review

HarvardHarvard

Murphy, PJ, Evans, DM, Horton, PN & Hursthouse, MB 2014, 'Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway', RSC Advances, vol. 4, no. 40, pp. 20744-20751. https://doi.org/10.1039/C4RA03031A

APA

Murphy, P. J., Evans, D. M., Horton, P. N., & Hursthouse, M. B. (2014). Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway. RSC Advances, 4(40), 20744-20751. https://doi.org/10.1039/C4RA03031A

CBE

Murphy PJ, Evans DM, Horton PN, Hursthouse MB. 2014. Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway. RSC Advances. 4(40):20744-20751. https://doi.org/10.1039/C4RA03031A

MLA

Murphy, P.J. et al. "Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway". RSC Advances. 2014, 4(40). 20744-20751. https://doi.org/10.1039/C4RA03031A

VancouverVancouver

Murphy PJ, Evans DM, Horton PN, Hursthouse MB. Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway. RSC Advances. 2014 Apr 28;4(40):20744-20751. doi: 10.1039/C4RA03031A

Author

Murphy, P.J. ; Evans, D.M. ; Horton, P.N. et al. / Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway. In: RSC Advances. 2014 ; Vol. 4, No. 40. pp. 20744-20751.

RIS

TY - JOUR

T1 - Preparation of an ABC tricyclic model of the cylindrospermopsin alkaloids via a biomimetically inspired pathway

AU - Murphy, P.J.

AU - Evans, D.M.

AU - Horton, P.N.

AU - Hursthouse, M.B.

PY - 2014/4/28

Y1 - 2014/4/28

N2 - Two tricyclic guanidine model compounds 28 and 29 have been prepared in 12 steps from 1,5-pentanediol using a biomimetic synthetic approach. The pivotal reaction in the sequence is a tethered Biginelli condensation between 21/22 and β-keto esters 23 and 24.

AB - Two tricyclic guanidine model compounds 28 and 29 have been prepared in 12 steps from 1,5-pentanediol using a biomimetic synthetic approach. The pivotal reaction in the sequence is a tethered Biginelli condensation between 21/22 and β-keto esters 23 and 24.

U2 - 10.1039/C4RA03031A

DO - 10.1039/C4RA03031A

M3 - Article

VL - 4

SP - 20744

EP - 20751

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

IS - 40

ER -