Synthesis 2020; 52(06): 834-846
DOI: 10.1055/s-0039-1690801
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© Georg Thieme Verlag Stuttgart · New York

Alkyl Tosylates as Alkylating Reagents in the Catellani Reaction

Qianwen Gao
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
,
Ze-Shui Liu
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
,
Yu Hua
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
,
Siwei Zhou
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
,
Hong-Gang Cheng
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
,
Qianghui Zhou
a   Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, P. R. of China   Email: hgcheng@whu.edu.cn   Email: qhzhou@whu.edu.cn
b   The Institute for Advanced Studies, Wuhan University, 430072 Wuhan, P. R. of China
› Author Affiliations
We are grateful to the National Natural Science Foundation of China (Grants 21602161, 21871213, and 21801193), for the startup funding from Wuhan University, and to the China Postdoctoral Science Foundation (No. 2018M642894, Z.-S. Liu) for financial support.
Further Information

Publication History

Received: 18 November 2019

Accepted after revision: 20 December 2019

Publication Date:
30 January 2020 (online)


Abstract

A cooperative catalytic system involving a Pd/XPhos complex and inexpensive 5-norbornene-2-carbonitrile that enables the use of alkyl tosylates as alkylating reagents in the Catellani reaction has been developed. This mild, scalable protocol is compatible with a range of readily available functionalized aryl iodides and alkyl tosylates, as well as terminating olefins (45 examples, up to 97% yield).

Supporting Information

 
  • References

    • 1a Trost BM. Science 1983; 219: 245
    • 1b Young IS, Baran PS. Nat. Chem. 2009; 1: 193
    • 1c Wender PA, Miller BL. Nature 2009; 460: 197

      For selected reviews, see:
    • 3a Catellani M. Top. Organomet. Chem. 2005; 14: 21
    • 3b Lautens M, Alberico D, Bressy C, Fang Y.-Q, Mariampillai B, Wilhelm T. Pure Appl. Chem. 2006; 78: 351
    • 3c Catellani M, Motti E, Della Ca’ N. Acc. Chem. Res. 2008; 41: 1512
    • 3d Martins A, Mariampillai B, Lautens M. Top. Curr. Chem. 2010; 292: 1
    • 3e Ferraccioli R. Synthesis 2013; 45: 581
    • 3f Ye J, Lautens M. Nat. Chem. 2015; 7: 863
    • 3g Zhu H, Ye C, Chen Z. Chin. J. Org. Chem. 2015; 35: 2291
    • 3h Della Ca’ N, Fontana M, Motti E, Catellani M. Acc. Chem. Res. 2016; 49: 1389
    • 3i Kim D.-S, Park W.-J, Jun C.-H. Chem. Rev. 2017; 117: 8977
    • 3j Liu Z.-S, Gao Q, Cheng H.-G, Zhou Q. Chem. Eur. J. 2018; 24: 15461
    • 3k Wegmann M, Henkel M, Bach T. Org. Biomol. Chem. 2018; 16: 5376
    • 3l Cheng H.-G, Chen S, Chen R, Zhou Q. Angew. Chem. Int. Ed. 2019; 58: 5832
    • 3m Wang J, Dong G. Chem. Rev. 2019; 119: 7478
  • 4 Catellani M, Frignani F, Rangoni A. Angew. Chem., Int. Ed. Engl. 1997; 36: 119
  • 5 Lautens M, Piguel S. Angew. Chem. Int. Ed. 2000; 39: 1045
  • 6 See ref. 3, and references cited therein.

    • For selected examples, see:
    • 7a Catellani M, Motti E, Baratta S. Org. Lett. 2001; 3: 3611
    • 7b Martins A, Candito DA, Lautens M. Org. Lett. 2010; 12: 5186
  • 8 Candito DA, Lautens M. Org. Lett. 2010; 12: 3312

    • For selected examples, see:
    • 9a Dong Z, Dong G. J. Am. Chem. Soc. 2013; 135: 18350
    • 9b Chen Z.-Y, Ye C.-Q, Zhu H, Zeng X.-P, Yuan J.-J. Chem. Eur. J. 2014; 20: 4237
    • 9c Ye C, Zhu H, Chen Z. J. Org. Chem. 2014; 79: 8900

      For selected examples, see:
    • 10a 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, Xu P.-F, Liang Y.-M. ACS Catal. 2015; 5: 4927
    • 10b Dong Z, Wang J, Ren Z, Dong G. Angew. Chem. Int. Ed. 2015; 54: 12664
    • 10c Huang Y, Zhu R, Zhao K, Gu Z. Angew. Chem. Int. Ed. 2015; 54: 12669
    • 10d Pan S, Wu F, Yu R, Chen W. J. Org. Chem. 2016; 81: 1558
    • 10e Sun F, Li M, He C, Wang B, Li B, Sui X, Gu Z. J. Am. Chem. Soc. 2016; 138: 7456
    • 10f Wang J, Zhang L, Dong Z, Dong G. Chem 2016; 1: 581
    • 10g Xu S, Jiang J, Ding L, Fu Y, Gu Z. Org. Lett. 2018; 20: 325
    • 10h Li R, Liu F, Dong G. Chem 2019; 5: 929
  • 11 Li R, Dong G. Angew. Chem. Int. Ed. 2018; 57: 1697
  • 12 Shen Y, Wu X.-X, Chen S, Xia Y, Liang Y.-M. Chem. Commun. 2018; 54: 2256
    • 13a Cheng H.-G, Wu C, Chen H, Chen R, Qian G, Geng Z, Wei Q, Xia Y, Zhang J, Zhang Y, Zhou Q. Angew. Chem. Int. Ed. 2018; 57: 3444
    • 13b Wu C, Cheng H.-G, Chen R, Chen H, Liu Z.-S, Zhang J, Zhang Y, Zhu Y, Geng Z, Zhou Q. Org. Chem. Front. 2018; 5: 2533
    • 13c Qian G, Bai M, Gao S, Chen H, Zhou S, Cheng H.-G, Yan W, Zhou Q. Angew. Chem. Int. Ed. 2018; 57: 10980
    • 13d Wu C, Yang X, Yan W, Shang Y, Cheng H.-G, Zhou Q. Org. Lett. 2019; 21: 8938
  • 14 Lv W, Wen S, Yu J, Cheng G. Org. Lett. 2018; 20: 4984
  • 16 Gao Q, Shang Y, Song F, Ye J, Liu Z.-S, Li L, Cheng H.-G, Zhou Q. J. Am. Chem. Soc. 2019; 141: 15986
  • 17 The iodide ion is gradually generated from the aryl iodide after its oxidative addition with Pd(0) catalyst: Maestri G, Motti E, Della Ca’ N, Malacria M, Derat E, Catellani M. J. Am. Chem. Soc. 2011; 133: 8574
  • 18 Aihara Y, Wuelbern J, Chatani N. Bull. Chem. Soc. Jpn. 2015; 88: 438
  • 19 Dong Z, Lu G, Wang J, Liu P, Dong G. J. Am. Chem. Soc. 2018; 140: 8551
  • 20 Wang J, Dong Z, Yang C, Dong G. Nat. Chem. 2019; 11: 1106
    • 21a Liu Z.-S, Qian G, Gao Q, Wang P, Cheng H.-G, Wei Q, Liu Q, Zhou Q. ACS Catal. 2018; 8: 4783
    • 21b Chen S, Liu Z.-S, Yang T, Hua Y, Zhou Z, Cheng H.-G, Zhou Q. Angew. Chem. Int. Ed. 2018; 57: 7161
    • 21c Gao Q, Liu Z.-S, Hua Y, Li L, Cheng H.-G, Cong H, Zhou Q. Chem. Commun. 2019; 55: 8816
    • 21d Wang P, Chen S, Zhou Z, Cheng H.-G, Zhou Q. Org. Lett. 2019; 21: 3323
    • 21e Chen S, Wang P, Cong H, Yang C, Zhou Q. Chem. Sci. 2019; 10: 8384
  • 22 See the Supporting Information for optimization details.
    • 23a Huang X, Anderson KW, Zim D, Jiang L, Klapars A, Buchwald SL. J. Am. Chem. Soc. 2003; 125: 6653
    • 23b Elsayed MS. A, Griggs B, Cushman M. Org. Lett. 2018; 20: 5228
  • 24 Aryl bromides survived this reaction, but are actually reactive under the conventional Pd/XPhos conditions; see ref. 21 and: Bruno NC, Niljianskul N, Buchwald SL. J. Org. Chem. 2014; 79: 4161
  • 25 For one example using methyl 4-nitrobenzenesulfonate as the electrophile, see ref. 19.