Double Mirozoki-Heck arylation of terminal alkenes using “ligand-free” pd catalytic systems
- Авторлар: Kurokhtina A.A1, Larina E.V1, Lagoda N.A1, Grigoryeva T.A1, Schmidt A.F1
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Мекемелер:
- Irkutsk State University
- Шығарылым: Том 59, № 10 (2023)
- Беттер: 1351-1356
- Бөлім: Articles
- URL: https://archivog.com/0514-7492/article/view/666175
- DOI: https://doi.org/10.31857/S0514749223100051
- EDN: https://elibrary.ru/OMIATP
- ID: 666175
Дәйексөз келтіру
Аннотация
The results of one-pot consecutive double arylation of terminal alkenes with aryl halides leading to three-substituted alkenes are presented. The advantages of the method when comparing with existing analogues are the combination of low reactive but available aryl bromides and aryl chlorides and «ligand-free» catalytic systems based on Pd(II) salt.
Негізгі сөздер
Авторлар туралы
A. Kurokhtina
Irkutsk State University
E. Larina
Irkutsk State University
N. Lagoda
Irkutsk State University
T. Grigoryeva
Irkutsk State University
A. Schmidt
Irkutsk State University
Email: aschmidt@chem.isu.ru
Әдебиет тізімі
- Zhao Y., Wang S., Shao H., Tan X., Chen R., Loh T.-P., Zhou J.S., Wu X. Org. Lett. 2023, 25, 4258-4263. doi: 10.1021/acs.orglett.3c01214
- Chen Y.-C., Wu C.-C., Liao W.-T., Liu L.-J., Tsai F.-Y. Catalysts. 2017, 7, 177. doi: 10.3390/catal7060177
- Xu D., Lu C., Chen W. Tetrahedron. 2012, 68, 1466-1474. doi: 10.1016/j.tet.2011.12.017
- Kim Y.-H., Jeong H.-C., Kim S.-H., Yang K., Kwon S.-K. Adv. Funct. Mater. 2005, 15, 1799-1805. doi: 10.1002/adfm.200500051
- Heck R.F. Synlett. 2006, 18, 2855-2860. doi: 10.1055/s-2006-951536
- Beletskaya I.P., Cheprakov A.V. Chem. Rev. 2000, 100, 3009-3066. doi: 10.1021/cr9903048
- Bangar P.G., Jawalkar P.R., Dumbre S.R., Raut P.K., Patil D.J., Tv N., Sudhakaran S., Iyer S. Synth. Commun. 2020, 50, 3796-3803. doi: 10.1080/00397911.2020.1811986
- Botella L., N�jera C. J. Org. Chem. 2005, 70, 4360-4369. doi: 10.1021/jo0502551
- Yan H., Sun P., Qu X., Lu L., Zhu Y., Yang H., Mao J. Synth. Commun. 2013, 43, 2773-2783. doi: 10.1080/00397911.2012.741743
- Ho S.V., McLaughlin J.M., Cue B.W., Dunn P.J. Green Chem. 2010, 12, 755. doi: 10.1039/b927443j
- Lucks S., Brunner H. Org. Proc. Res. Dev. 2017, 21, 1835-1842. doi: 10.1021/acs.oprd.7b00279
- Taylor J.G., Da Silva Ribeiro R., Correia C.R.D. Tetrahedron Lett. 2011, 52, 3861-3864. doi: 10.1016/j.tetlet.2011.05.039
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