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An intramolecular cycloaddition approach to the kauranoid family of diterpene metabolites

Brenda Callebaut (UGent) , Jan Hullaert (UGent) , Kristof Van Hecke (UGent) and Johan Winne (UGent)
(2019) ORGANIC LETTERS. 21(1). p.310-314
Author
Organization
Abstract
Synthetic studies toward the ent-kauranoid family of diterpene natural products are reported. An intramolecular (4 + 3) cycloaddition allows the direct elaboration of diverse natural product frameworks, encompassing a challenging bicyclo[3.2.1]octane core. The established routes comprise only a few synthetic operations (3-5 steps), transforming a range of simple starting materials into the tetracyclic scaffolds that are commonly found in many ent-kaurene metabolites.
Keywords
GIBBERELLINS, ROUTE

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Citation

Please use this url to cite or link to this publication:

MLA
Callebaut, Brenda et al. “An Intramolecular Cycloaddition Approach to the Kauranoid Family of Diterpene Metabolites.” ORGANIC LETTERS 21.1 (2019): 310–314. Print.
APA
Callebaut, B., Hullaert, J., Van Hecke, K., & Winne, J. (2019). An intramolecular cycloaddition approach to the kauranoid family of diterpene metabolites. ORGANIC LETTERS, 21(1), 310–314.
Chicago author-date
Callebaut, Brenda, Jan Hullaert, Kristof Van Hecke, and Johan Winne. 2019. “An Intramolecular Cycloaddition Approach to the Kauranoid Family of Diterpene Metabolites.” Organic Letters 21 (1): 310–314.
Chicago author-date (all authors)
Callebaut, Brenda, Jan Hullaert, Kristof Van Hecke, and Johan Winne. 2019. “An Intramolecular Cycloaddition Approach to the Kauranoid Family of Diterpene Metabolites.” Organic Letters 21 (1): 310–314.
Vancouver
1.
Callebaut B, Hullaert J, Van Hecke K, Winne J. An intramolecular cycloaddition approach to the kauranoid family of diterpene metabolites. ORGANIC LETTERS. 2019;21(1):310–4.
IEEE
[1]
B. Callebaut, J. Hullaert, K. Van Hecke, and J. Winne, “An intramolecular cycloaddition approach to the kauranoid family of diterpene metabolites,” ORGANIC LETTERS, vol. 21, no. 1, pp. 310–314, 2019.
@article{8586631,
  abstract     = {Synthetic studies toward the ent-kauranoid family of diterpene natural products are reported. An intramolecular (4 + 3) cycloaddition allows the direct elaboration of diverse natural product frameworks, encompassing a challenging bicyclo[3.2.1]octane core. The established routes comprise only a few synthetic operations (3-5 steps), transforming a range of simple starting materials into the tetracyclic scaffolds that are commonly found in many ent-kaurene metabolites.},
  author       = {Callebaut, Brenda and Hullaert, Jan and Van Hecke, Kristof and Winne, Johan},
  issn         = {1523-7060},
  journal      = {ORGANIC LETTERS},
  keywords     = {GIBBERELLINS,ROUTE},
  language     = {eng},
  number       = {1},
  pages        = {310--314},
  title        = {An intramolecular cycloaddition approach to the kauranoid family of diterpene metabolites},
  url          = {http://dx.doi.org/10.1021/acs.orglett.8b03810},
  volume       = {21},
  year         = {2019},
}

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