TY  - DATA
AU  - Husinec, Suren
AU  - Savić, Vladimir
AU  - Simić, Milena R.
AU  - Tešević, Vele
AU  - Vidović, Dragoslav
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3572
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Supplementary data for article: Husinec, S.; Savić, V.; Simić, M. R.; Tešević, V.; Vidovic, D. Annulations of Isoquinoline and Beta-Carboline Ring Systems: Synthesis of 8-Oxoprotoberberine Derivatives. Tetrahedron Letters 2011, 52 (21), 2733–2736. https://doi.org/10.1016/j.tetlet.2011.03.085
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3572
ER  - 

@misc{
author = "Husinec, Suren and Savić, Vladimir and Simić, Milena R. and Tešević, Vele and Vidović, Dragoslav",
year = "2011",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Supplementary data for article: Husinec, S.; Savić, V.; Simić, M. R.; Tešević, V.; Vidovic, D. Annulations of Isoquinoline and Beta-Carboline Ring Systems: Synthesis of 8-Oxoprotoberberine Derivatives. Tetrahedron Letters 2011, 52 (21), 2733–2736. https://doi.org/10.1016/j.tetlet.2011.03.085",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3572"
}

Husinec, S., Savić, V., Simić, M. R., Tešević, V.,& Vidović, D.. (2011). Supplementary data for article: Husinec, S.; Savić, V.; Simić, M. R.; Tešević, V.; Vidovic, D. Annulations of Isoquinoline and Beta-Carboline Ring Systems: Synthesis of 8-Oxoprotoberberine Derivatives. Tetrahedron Letters 2011, 52 (21), 2733–2736. https://doi.org/10.1016/j.tetlet.2011.03.085. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford..
https://hdl.handle.net/21.15107/rcub_cherry_3572

Husinec S, Savić V, Simić MR, Tešević V, Vidović D. Supplementary data for article: Husinec, S.; Savić, V.; Simić, M. R.; Tešević, V.; Vidovic, D. Annulations of Isoquinoline and Beta-Carboline Ring Systems: Synthesis of 8-Oxoprotoberberine Derivatives. Tetrahedron Letters 2011, 52 (21), 2733–2736. https://doi.org/10.1016/j.tetlet.2011.03.085. in Tetrahedron Letters. 2011;.
https://hdl.handle.net/21.15107/rcub_cherry_3572 .

Husinec, Suren, Savić, Vladimir, Simić, Milena R., Tešević, Vele, Vidović, Dragoslav, "Supplementary data for article: Husinec, S.; Savić, V.; Simić, M. R.; Tešević, V.; Vidovic, D. Annulations of Isoquinoline and Beta-Carboline Ring Systems: Synthesis of 8-Oxoprotoberberine Derivatives. Tetrahedron Letters 2011, 52 (21), 2733–2736. https://doi.org/10.1016/j.tetlet.2011.03.085" in Tetrahedron Letters (2011),
https://hdl.handle.net/21.15107/rcub_cherry_3572 .

TY  - JOUR
AU  - Husinec, Suren
AU  - Savić, Vladimir
AU  - Simić, Milena R.
AU  - Tešević, Vele
AU  - Vidović, Dragoslav
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1342
AB  - Annulation processes of isoquinoline and p-carboline compounds have been investigated leading to synthetic routes for the preparation of 8-oxoprotoberberine derivatives. The key steps combined a diene formation/Diels-Alder cycloaddition reaction to afford the targeted polycyclic skeletons. Further oxidative transformations of the cycloadducts produced the 8-oxoprotoberberine type products. The alkaloids of this class are important natural products with a wide range of biological activity and the synthethic methodology described in this paper could prove to be useful for the preparation of the D-ring functionalised derivatives.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - Annulations of isoquinoline and beta-carboline ring systems: synthesis of 8-oxoprotoberberine derivatives
VL  - 52
IS  - 21
SP  - 2733
EP  - 2736
DO  - 10.1016/j.tetlet.2011.03.085
ER  - 

@article{
author = "Husinec, Suren and Savić, Vladimir and Simić, Milena R. and Tešević, Vele and Vidović, Dragoslav",
year = "2011",
abstract = "Annulation processes of isoquinoline and p-carboline compounds have been investigated leading to synthetic routes for the preparation of 8-oxoprotoberberine derivatives. The key steps combined a diene formation/Diels-Alder cycloaddition reaction to afford the targeted polycyclic skeletons. Further oxidative transformations of the cycloadducts produced the 8-oxoprotoberberine type products. The alkaloids of this class are important natural products with a wide range of biological activity and the synthethic methodology described in this paper could prove to be useful for the preparation of the D-ring functionalised derivatives.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "Annulations of isoquinoline and beta-carboline ring systems: synthesis of 8-oxoprotoberberine derivatives",
volume = "52",
number = "21",
pages = "2733-2736",
doi = "10.1016/j.tetlet.2011.03.085"
}

Husinec, S., Savić, V., Simić, M. R., Tešević, V.,& Vidović, D.. (2011). Annulations of isoquinoline and beta-carboline ring systems: synthesis of 8-oxoprotoberberine derivatives. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 52(21), 2733-2736.
https://doi.org/10.1016/j.tetlet.2011.03.085

Husinec S, Savić V, Simić MR, Tešević V, Vidović D. Annulations of isoquinoline and beta-carboline ring systems: synthesis of 8-oxoprotoberberine derivatives. in Tetrahedron Letters. 2011;52(21):2733-2736.
doi:10.1016/j.tetlet.2011.03.085 .

Husinec, Suren, Savić, Vladimir, Simić, Milena R., Tešević, Vele, Vidović, Dragoslav, "Annulations of isoquinoline and beta-carboline ring systems: synthesis of 8-oxoprotoberberine derivatives" in Tetrahedron Letters, 52, no. 21 (2011):2733-2736,
https://doi.org/10.1016/j.tetlet.2011.03.085 . .