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Synlett 2021; 32(11): 1049-1052
DOI: 10.1055/s-0040-1706029
DOI: 10.1055/s-0040-1706029
synpacts
Alkylcarbagermatranes Permit an Alkylation-Terminated Catellani Reaction
This work was supported by NSFC (21871239), Fundamental Research Funds for the Central Universities (WK2060190081), and the Youth Innovation Promotion Association of the Chinese Academy of Sciences (Y201987).
Abstract
We highlight our recent researches on an alkylation-terminated Catellani reaction using alkylcarbagermatranes. This strategy highlights the unique structure and property of alkylcarbagermatranes and also fills the gap in the Catellani reaction where alkylation termination was missing.
Publication History
Received: 28 January 2021
Accepted after revision: 17 February 2021
Article published online:
01 April 2021
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References
- 1a Ye J, Lautens M. Nat. Chem. 2015; 7: 863
- 1b Della Ca’ N, Fontana M, Motti E, Catellani M. Acc. Chem. Res. 2016; 49: 1389
- 1c Wang J, Dong G. Chem. Rev. 2019; 119: 7478
- 2 Catellani M, Frignani F, Rangoni A. Angew. Chem. Int. Ed. 1997; 36: 119
- 3 Catellani M, Motti E, Minari M. Chem. Commun. 2000; 157
- 4 Motti E, Rossetti M, Bocelli G, Catellani M. J. Organomet. Chem. 2004; 689: 3741
- 5 Wilhelm T, Lautens M. Org. Lett. 2005; 7: 4053
- 6a Motti E, Ippomei G, Deledda S, Catellani M. Synthesis 2003; 2671
- 6b Motti E, Mignozzi A, Catellani M. J. Mol. Catal. A: Chem. 2003; 204: 115
- 7 Dong Z, Dong G. J. Am. Chem. Soc. 2013; 135: 18350
- 8a Dong Z, Wang J, Ren Z, Dong G. Angew. Chem. Int. Ed. 2015; 54: 12664
- 8b Huang Y, Zhu R, Zhao K, Gu Z. Angew. Chem. Int. Ed. 2015; 54: 12669
- 8c Zhou P.-X, Ye Y.-Y, Liu C, Zhao L.-B, Hou J.-Y, Chen D.-Q, Tang Q, Wang A.-Q, Zhang J.-Y, Huang Q.-X. ACS Catal. 2015; 5: 4927
- 9a Zhang B.-S, Hua H.-L, Gao L.-Y, Liu C, Qiu Y.-F, Zhou P.-X, Zhou Z.-Z, Zhao J.-H, Liang Y.-M. Org. Chem. Front. 2017; 4: 1376
- 9b Zhang B.-S, Li Y, An Y, Zhang Z, Liu C, Wang X.-G, Liang Y.-M. ACS Catal. 2018; 8: 11827
- 10 Wilson JE. Tetrahedron Lett. 2016; 57: 5053
- 11 Wang J, Dong Z, Yang C, Dong G. Nat. Chem. 2019; 11: 1106
- 12 Jiang W.-T, Xu M.-Y, Yang S, Xie X.-Y, Xiao B. Angew. Chem. Int. Ed. 2020; 59: 20450
- 13a Jiang W.-T, Yang S, Xu M.-Y, Xie X.-Y, Xiao B. Chem. Sci. 2020; 11: 488
- 13b Xu M.-Y, Jiang W.-T, Li Y, Xu Q.-H, Zhou Q.-L, Yang S, Xiao B. J. Am. Chem. Soc. 2019; 141: 7582
- 14a Fricke C, Deckers K, Schoenebeck F. Angew. Chem. Int. Ed. 2020; 59: 18717
- 14b Sherborne GJ, Gevondian AG, Funes-Ardoiz I, Dahiya A, Fricke C, Schoenebeck F. Angew. Chem. Int. Ed. 2020; 59: 15543
- 14c Dahiya A, Fricke C, Schoenebeck F. J. Am. Chem. Soc. 2020; 142: 7754
- 14d Fricke C, Sherborne GJ, Funes-Ardoiz I, Senol E, Guven S, Schoenebeck F. Angew. Chem. Int. Ed. 2019; 58: 17788
- 14e Fricke C, Dahiya A, Reid WB, Schoenebeck F. ACS Catal. 2019; 9: 9231 corrigendum: ACS Catal. 2019, 9, 10232
- 15 Evans GB, Furneaux RH, Gravestock MB, Lynch GP, Scott GK. Bioorg. Med. Chem. 1999; 7: 1953
For recent research on carbagermatranes, see:
For recent research on other organogermanes, see: