Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine
Само за регистроване кориснике
2015
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The intramolecular Heck reaction has been examined for the preparation of the core bicyclic structure of corialstonidine. Initial attempts to cyclise a vinyl iodide moiety onto a cyclic allyl alcohol were complicated by various side reactions. However, the corresponding process performed under reductive conditions on a conjugated ketone, obtained from the cyclic allyl alcohol, afforded the desired bicyclo[3.2.1] derivative. This compound possesses the skeletal features of the carbocyclic fragment of corialstonidine and is suitable for further transformations aimed towards the synthesis of the natural product or its derivatives.
Кључне речи:
Heck reaction / Corialstonidine / Bicyclic ketoneИзвор:
Tetrahedron Letters, 2015, 56, 19, 2529-2532Издавач:
- Oxford : Pergamon-Elsevier Science Ltd
Финансирање / пројекти:
DOI: 10.1016/j.tetlet.2015.03.129
ISSN: 0040-4039
WoS: 000353751000035
Scopus: 2-s2.0-84937762963
Институција/група
IHTMTY - JOUR AU - Tasic, Gordana AU - Maslak, Veselin AU - Husinec, Suren AU - Todorović, Nina AU - Savić, Vladimir PY - 2015 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/1740 AB - The intramolecular Heck reaction has been examined for the preparation of the core bicyclic structure of corialstonidine. Initial attempts to cyclise a vinyl iodide moiety onto a cyclic allyl alcohol were complicated by various side reactions. However, the corresponding process performed under reductive conditions on a conjugated ketone, obtained from the cyclic allyl alcohol, afforded the desired bicyclo[3.2.1] derivative. This compound possesses the skeletal features of the carbocyclic fragment of corialstonidine and is suitable for further transformations aimed towards the synthesis of the natural product or its derivatives. PB - Oxford : Pergamon-Elsevier Science Ltd T2 - Tetrahedron Letters T1 - Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine VL - 56 IS - 19 SP - 2529 EP - 2532 DO - 10.1016/j.tetlet.2015.03.129 ER -
@article{ author = "Tasic, Gordana and Maslak, Veselin and Husinec, Suren and Todorović, Nina and Savić, Vladimir", year = "2015", abstract = "The intramolecular Heck reaction has been examined for the preparation of the core bicyclic structure of corialstonidine. Initial attempts to cyclise a vinyl iodide moiety onto a cyclic allyl alcohol were complicated by various side reactions. However, the corresponding process performed under reductive conditions on a conjugated ketone, obtained from the cyclic allyl alcohol, afforded the desired bicyclo[3.2.1] derivative. This compound possesses the skeletal features of the carbocyclic fragment of corialstonidine and is suitable for further transformations aimed towards the synthesis of the natural product or its derivatives.", publisher = "Oxford : Pergamon-Elsevier Science Ltd", journal = "Tetrahedron Letters", title = "Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine", volume = "56", number = "19", pages = "2529-2532", doi = "10.1016/j.tetlet.2015.03.129" }
Tasic, G., Maslak, V., Husinec, S., Todorović, N.,& Savić, V.. (2015). Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine. in Tetrahedron Letters Oxford : Pergamon-Elsevier Science Ltd., 56(19), 2529-2532. https://doi.org/10.1016/j.tetlet.2015.03.129
Tasic G, Maslak V, Husinec S, Todorović N, Savić V. Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine. in Tetrahedron Letters. 2015;56(19):2529-2532. doi:10.1016/j.tetlet.2015.03.129 .
Tasic, Gordana, Maslak, Veselin, Husinec, Suren, Todorović, Nina, Savić, Vladimir, "Study of the intramolecular Heck reaction: synthesis of the bicyclic core of corialstonidine" in Tetrahedron Letters, 56, no. 19 (2015):2529-2532, https://doi.org/10.1016/j.tetlet.2015.03.129 . .