Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate
Само за регистроване кориснике
2013
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
Cyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate.
Кључне речи:
Organic synthesis / Indium / Heck reaction / Allylation / Aldol reactionИзвор:
Tetrahedron Letters, 2013, 54, 48, 6624-6626Издавач:
- Pergamon-Elsevier Science Ltd, Oxford
DOI: 10.1016/j.tetlet.2013.09.115
ISSN: 0040-4039
WoS: 000326613600054
Scopus: 2-s2.0-84886791811
Институција/група
Institut za molekularnu genetiku i genetičko inženjerstvoTY - JOUR AU - Bigović, Miljan AU - Škaro Bogojević, Sanja AU - Maslak, Veselin AU - Saicić, Radomir N. PY - 2013 UR - https://imagine.imgge.bg.ac.rs/handle/123456789/668 AB - Cyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate. PB - Pergamon-Elsevier Science Ltd, Oxford T2 - Tetrahedron Letters T1 - Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate EP - 6626 IS - 48 SP - 6624 VL - 54 DO - 10.1016/j.tetlet.2013.09.115 ER -
@article{ author = "Bigović, Miljan and Škaro Bogojević, Sanja and Maslak, Veselin and Saicić, Radomir N.", year = "2013", abstract = "Cyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate.", publisher = "Pergamon-Elsevier Science Ltd, Oxford", journal = "Tetrahedron Letters", title = "Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate", pages = "6626-6624", number = "48", volume = "54", doi = "10.1016/j.tetlet.2013.09.115" }
Bigović, M., Škaro Bogojević, S., Maslak, V.,& Saicić, R. N.. (2013). Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters Pergamon-Elsevier Science Ltd, Oxford., 54(48), 6624-6626. https://doi.org/10.1016/j.tetlet.2013.09.115
Bigović M, Škaro Bogojević S, Maslak V, Saicić RN. Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate. in Tetrahedron Letters. 2013;54(48):6624-6626. doi:10.1016/j.tetlet.2013.09.115 .
Bigović, Miljan, Škaro Bogojević, Sanja, Maslak, Veselin, Saicić, Radomir N., "Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate" in Tetrahedron Letters, 54, no. 48 (2013):6624-6626, https://doi.org/10.1016/j.tetlet.2013.09.115 . .