Enantioselective synthesis of the strigolactone mimic (+)-GR24

Liam J. Bromhead; Johan Visser; Christopher S.P. McErlean

doi:10.1021/jo402722p

Enantioselective synthesis of the strigolactone mimic (+)-GR24

Liam J. Bromhead, Johan Visser, Christopher S.P. McErlean

The University of Sydney, School of Chemistry

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

Abstract

A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A-C ring system.

Original language	English
Pages (from-to)	1516 - 1520
Number of pages	5
Journal	The Journal of Organic Chemistry
Volume	79
Issue number	3
DOIs	https://doi.org/10.1021/jo402722p
Publication status	Published - 17 Jan 2014
Externally published	Yes

Keywords

enantioselective synthesis
strigolactone

Access to Document

10.1021/jo402722p

7 Article

Third-Generation Light-Driven Symmetric Molecular Motors
Kistemaker, J. C. M., Štacko, P., Roke, D., Wolters, A. T., Heideman, H., Chang, M.-C., Van der Meulen, P., Visser, J., Otten, E. & Feringa, B. L., 19 Jul 2017, In: Journal of the American Chemical Society. 139, 28, p. 9650 - 9661 12 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
From chaos to order: Chain-length dependence of the free energy of formation of meso-tetraalkylporphyrin self-assembled monolayer polymorphs
Reimers, J. R., Panduwinata, D., Visser, J., Chin, Y., Tang, C., Goerigk, L., Ford, M. J., Baker, M., Sum, T.-J., Coenen, M. J. J., Hendriksen, B. L. M., Elemans, J. A. A. W., Hush, N. S. & Crossley, M. J., 5 Jan 2016, In: Journal of Physical Chemistry C. 120, 3, p. 1739 - 1748 10 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access
A priori calculations of the free energy of formation from solution of polymorphic self-Assembled monolayers
Reimers, J. R., Panduwinata, D., Visser, J., Tang, C., Goerigk, L., Ford, M. J., Sintic, M., Sum, T.-J., Coenen, M. J. J., Hendriksen, B. L. M., Elemans, J. A. A. W., Hush, N. S. & Crossley, M. J., 28 Oct 2015, In: Proceedings of the National Academy of Sciences. 112, 45, p. E6101 - E6110 10 p.
Research output: Contribution to journal › Article › Academic › peer-review

Open Access

Cite this

@article{3d503196648e4be2b7638342085e2e87,

title = "Enantioselective synthesis of the strigolactone mimic (+)-GR24",

abstract = "A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A-C ring system.",

keywords = "enantioselective synthesis, strigolactone, asymmetrische synthese, strigolactonen",

author = "Bromhead, {Liam J.} and Johan Visser and McErlean, {Christopher S.P.}",

year = "2014",

month = jan,

day = "17",

doi = "10.1021/jo402722p",

language = "English",

volume = "79",

pages = "1516 -- 1520",

journal = "The Journal of Organic Chemistry",

issn = "1520-6904",

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AU - Bromhead, Liam J.

AU - Visser, Johan

AU - McErlean, Christopher S.P.

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Y1 - 2014/1/17

N2 - A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A-C ring system.

AB - A short and cost-effective synthesis of the important strigolactone analogue (+)-GR24 is described. Central to this new approach is the concise, enantioselective synthesis of the A-C ring system.

KW - enantioselective synthesis

KW - strigolactone

KW - asymmetrische synthese

KW - strigolactonen

U2 - 10.1021/jo402722p

DO - 10.1021/jo402722p

M3 - Article

SN - 1520-6904

VL - 79

SP - 1516

EP - 1520

JO - The Journal of Organic Chemistry

JF - The Journal of Organic Chemistry

IS - 3

ER -

Enantioselective synthesis of the strigolactone mimic (+)-GR24

Abstract

Keywords

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Research output

Third-Generation Light-Driven Symmetric Molecular Motors

From chaos to order: Chain-length dependence of the free energy of formation of meso-tetraalkylporphyrin self-assembled monolayer polymorphs

A priori calculations of the free energy of formation from solution of polymorphic self-Assembled monolayers

Cite this