Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett
DOI: 10.1055/s-0043-1763636
DOI: 10.1055/s-0043-1763636
synpacts
Methods for the Synthesis of 1-Indanones Containing a β-Quaternary Carbon Center
Financial support from the National Natural Science Foundation of China (Grant No. 22071051) and Hunan Normal University is greatly appreciated.
![](https://www.thieme-connect.de/media/synlett/EFirst/lookinside/thumbnails/st-2023-p0455-sp_10-1055_s-0043-1763636-1.jpg)
Abstract
This article traces the development of synthetic routes toward 1-indanones containing a β-quaternary carbon center. The recent advancement in the regio- and chemoselective formal (4+1) carbocyclization of chalcones with internal alkynes via rhodium(III) catalysis for the synthesis of 1-indanones is highlighted.
Publication History
Received: 08 October 2023
Accepted after revision: 23 October 2023
Article published online:
30 November 2023
© 2023. Thieme. All rights reserved
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Patil SA, Patil R, Patil SA. Eur. J. Med. Chem. 2017; 138: 182
- 2 Marsais F, Levacher V, Papamicael C, Bohn P, Peauger L, Gembus V, Fur NL, Dumartin-Lepine M. WO2014114742A1, 2014
- 3 Leoni LM, Hamel E, Genini D, Shih H, Carrera CJ, Cottam HB, Carson DA. J. Natl. Cancer Inst. 2000; 92: 217
- 4 Hao X.-D, Chang J, Qin B.-Y, Zhong C, Chu Z.-B, Huang J, Zhou W.-J, Sun X. Eur. J. Med. Chem. 2015; 102: 26
- 5 Das S, Dutta A. New J. Chem. 2021; 45: 4545
- 6 Büschleb M, Dorich S, Hanessian S, Tao D, Schenthal KB, Overman LE. Angew. Chem. Int. Ed. 2016; 55: 4156
- 7 Quasdorf KW, Overman LE. Science 2014; 516: 181
- 8 Fuji K. Chem. Rev. 1993; 93: 2037
- 9 Shintani R, Hayashi T. Org. Lett. 2005; 7: 2071
- 10 Shintani R, Takatsu K, Hayashi T. Angew. Chem. Int. Ed. 2007; 46: 3735
- 11 Matsuda T, Shigeno M, Makino M, Murakami M. Org. Lett. 2006; 8: 3379
- 12 Seiser T, Cathomen G, Cramer N. Synlett 2010; 11: 1699
- 13 Sun Y.-L, Wang X.-B, Sun F.-N, Chen Q.-Q, Cao J, Xu Z, Xu L.-W. Angew. Chem. Int. Ed. 2019; 58: 6747
- 14 Sun F.-N, Yang W.-C, Chen X.-B, Sun Y.-L, Cao J, Xua Z, Xu L.-W. Chem. Sci. 2019; 10: 7579
- 15 Yang W.-C, Chen X.-B, Song K.-L, Wu B, Gan W.-E, Zheng Z.-J, Cao J, Xu L.-W. Org. Lett. 2021; 23: 1309
- 16 Xia Y, Lu G, Liu P, Dong G. Nature 2016; 539: 546
- 17 Xia Y, Wang J, Dong G. Angew. Chem. Int. Ed. 2017; 56: 2376
- 18 Yu S, Liu S, Lan Y, Wan B, Li X. J. Am. Chem. Soc. 2015; 137: 1623
- 19 Lou J, Han W, Liu Z, Xiao J. Org. Chem. Front. 2021; 8: 1447
- 20 Cai S.-L, Yan L, Yang C, Sheng J, Wang X.-S. ACS Catal. 2019; 9: 10299
- 21 Song S, Lai Y, Tuo Z, Zhong J, Zhou W. Angew. Chem. Int. Ed. 2023; 62: e202305983
- 22 Ye B, Cramer N. Acc. Chem. Res. 2015; 48: 1308