Home > Research > Publications & Outputs > Stereocontrolled synthesis of the aconitine D r...

Research

Links

Text available via DOI:

View graph of relations

Stereocontrolled synthesis of the aconitine D ring from d -glucose

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Published

Standard

Stereocontrolled synthesis of the aconitine D ring from d -glucose. / Pocock, Ian A.; Doulcet, Julien; Rice, Craig R. et al.
In: Organic and Biomolecular Chemistry , Vol. 22, No. 21, 03.05.2024, p. 4347-4352.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Pocock, IA, Doulcet, J, Rice, CR, Sweeney, JB & Gill, DM 2024, 'Stereocontrolled synthesis of the aconitine D ring from d -glucose', Organic and Biomolecular Chemistry , vol. 22, no. 21, pp. 4347-4352. https://doi.org/10.1039/d4ob00561a

APA

Pocock, I. A., Doulcet, J., Rice, C. R., Sweeney, J. B., & Gill, D. M. (2024). Stereocontrolled synthesis of the aconitine D ring from d -glucose. Organic and Biomolecular Chemistry , 22(21), 4347-4352. https://doi.org/10.1039/d4ob00561a

Vancouver

Pocock IA, Doulcet J, Rice CR, Sweeney JB, Gill DM. Stereocontrolled synthesis of the aconitine D ring from d -glucose. Organic and Biomolecular Chemistry . 2024 May 3;22(21):4347-4352. Epub 2024 May 3. doi: 10.1039/d4ob00561a

Author

Pocock, Ian A. ; Doulcet, Julien ; Rice, Craig R. et al. / Stereocontrolled synthesis of the aconitine D ring from d -glucose. In: Organic and Biomolecular Chemistry . 2024 ; Vol. 22, No. 21. pp. 4347-4352.

Bibtex

@article{a4c973e94e3840d382e214aba49a0c70,
title = "Stereocontrolled synthesis of the aconitine D ring from d -glucose",
abstract = "All five oxygen substituents and all six skeletal carbon atoms of the aconitine D ring are derived from d-glucose in a fully stereocontrolled synthesis featuring an enelactone to diketone rearrangement.",
author = "Pocock, {Ian A.} and Julien Doulcet and Rice, {Craig R.} and Sweeney, {Joseph B.} and Gill, {Duncan M.}",
year = "2024",
month = may,
day = "3",
doi = "10.1039/d4ob00561a",
language = "English",
volume = "22",
pages = "4347--4352",
journal = "Organic and Biomolecular Chemistry ",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "21",

}

RIS

TY - JOUR

T1 - Stereocontrolled synthesis of the aconitine D ring from d -glucose

AU - Pocock, Ian A.

AU - Doulcet, Julien

AU - Rice, Craig R.

AU - Sweeney, Joseph B.

AU - Gill, Duncan M.

PY - 2024/5/3

Y1 - 2024/5/3

N2 - All five oxygen substituents and all six skeletal carbon atoms of the aconitine D ring are derived from d-glucose in a fully stereocontrolled synthesis featuring an enelactone to diketone rearrangement.

AB - All five oxygen substituents and all six skeletal carbon atoms of the aconitine D ring are derived from d-glucose in a fully stereocontrolled synthesis featuring an enelactone to diketone rearrangement.

U2 - 10.1039/d4ob00561a

DO - 10.1039/d4ob00561a

M3 - Journal article

VL - 22

SP - 4347

EP - 4352

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

IS - 21

ER -