Synlett 2014; 25(5): 608-614
DOI: 10.1055/s-0033-1340549
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© Georg Thieme Verlag Stuttgart · New York

Employing Arynes in Transition-Metal-Free, N-Heterocycle- Initiated Multicomponent Reactions

Anup Bhunia
Organic Chemistry Division, CSIR-National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune 411008, India   Fax: +91(20)25902629   Email: at.biju@ncl.res.in
,
Akkattu T. Biju*
Organic Chemistry Division, CSIR-National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune 411008, India   Fax: +91(20)25902629   Email: at.biju@ncl.res.in
› Author Affiliations
Further Information

Publication History

Received: 06 November 2013

Accepted after revision: 03 December 2013

Publication Date:
14 January 2014 (online)


Abstract

Transition-metal-free multicomponent reactions involving arynes, N-heterocycles, and various carbonyl compounds have been reported. With (iso)quinoline as the nucleophile and carbonyl compounds, such as aldehydes, ketones, and N-substituted isatins as electrophiles, the reaction afforded oxazino (iso)quinoline derivatives and the reaction proceeded via 1,4-dipolar intermediates. Interestingly, when the nucleophilic trigger used is pyridine, the reaction furnished indolin-2-one derivatives, and it is probable that the reaction proceeds via a pyridylidene intermediate.

 
  • References and Notes


    • For recent reviews on aryne chemistry, see:
    • 1a Bhunia A, Yetra SR, Biju AT. Chem. Soc. Rev. 2012; 41: 3140
    • 1b Tadross PM, Stoltz BM. Chem. Rev. 2012; 112: 3550
    • 1c Gampe CM, Carreira EM. Angew. Chem. Int. Ed. 2012; 51: 3766
    • 1d Wu C, Shi F. Asian J. Org. Chem. 2013; 2: 116
    • 1e Dubrovskiy AV, Markina NA, Larock RC. Org. Biomol. Chem. 2013; 11: 191
    • 1f Okuma K. Heterocycles 2012; 85: 515
    • 1g Yoshida H, Takaki K. Synlett 2012; 23: 1725
    • 1h Chen Y, Larock RC. Arylation Reactions Involving the Formation of Arynes. In Modern Arylation Methods. Ackermann L. Wiley-VCH; Weinheim: 2009: 401
    • 1i Sanz R. Org. Prep. Proced. Int. 2008; 40: 215
    • 1j Wenk HH, Winkler M, Sander W. Angew. Chem. Int. Ed. 2003; 42: 502
    • 1k Pellissier H, Santelli M. Tetrahedron 2003; 59: 701
    • 2a Himeshima Y, Sonoda T, Kobayashi H. Chem. Lett. 1983; 1211

    • See also:
    • 2b Peña D, Cobas A, Pérez D, Guitián E. Synthesis 2002; 1454

      For a recent review, see:
    • 3a Pérez D, Peña D, Guitián E. Eur. J. Org. Chem. 2013; 5981

    • For selected recent reports, see:
    • 3b Rodríguez-Lojo D, Pérez D, Peña D, Guitián E. Chem. Commun. 2013; 49: 6274
    • 3c Goetz AE, Garg NK. Nat. Chem. 2013; 5: 54
    • 3d Singh G, Kumar R, Swett J, Zajc B. Org. Lett. 2013; 15: 4086
    • 3e Kaicharla T, Bhojgude SS, Biju AT. Org. Lett. 2012; 14: 6238
    • 3f Bhojgude SS, Kaicharla T, Bhunia A, Biju AT. Org. Lett. 2012; 14: 4098
    • 3g Li J, Wang N, Li C, Jia X. Org. Lett. 2012; 14: 4994

      For selected recent reports, see:
    • 4a Bhojgude SS, Kaicharla T, Biju AT. Org. Lett. 2013; 15: 5452
    • 4b Hendrick CE, McDonald SL, Wang Q. Org. Lett. 2013; 15: 3444
    • 4c Yoshida H, Yoshida R, Takaki K. Angew. Chem. Int. Ed. 2013; 52: 8629
    • 4d Stephens D, Zhang Y, Cormier M, Chavez G, Arman H, Larionov OV. Chem. Commun. 2013; 49: 6558
    • 4e Vaidya SD, Argade NP. Org. Lett. 2013; 15: 4006
    • 4f Dhokale RA, Mhaske SB. Org. Lett. 2013; 15: 2218
    • 4g Kim J, Stoltz BM. Tetrahedron Lett. 2012; 53: 4994
    • 4h Fang Y, Rogness DC, Larock RC, Shi F. J. Org. Chem. 2012; 77: 6262
    • 4i Okuma K, Itoyama R, Sou A, Nagahora N, Shioj K. Chem. Commun. 2012; 48: 11145
    • 4j Rodríguez-Lojo D, Cobas A, Peña D, Pérez D, Guitián E. Org. Lett. 2012; 14: 1363
    • 4k Mohanan K, Coquerel Y, Rodriguez J. Org. Lett. 2012; 14: 4686
  • 5 For a highlight on transition-metal-free aryne MCR, see: Bhojgude SS, Biju AT. Angew. Chem. Int. Ed. 2012; 51: 1520
    • 6a Bhunia A, Roy T, Pachfule P, Rajamohanan PR, Biju AT. Angew. Chem. Int. Ed. 2013; 52: 10040
    • 6b Bhunia A, Porwal D, Gonnade RG, Biju AT. Org. Lett. 2013; 15: 4620
    • 7a Meyers AI, Pansegrau PD. Tetrahedron Lett. 1983; 24: 4935
    • 7b Meyers AI, Pansegrau PD. J. Chem. Soc., Chem. Commun. 1985; 690
    • 7c Tripathy S, LeBlanc R, Durst T. Org. Lett. 1999; 1: 1973
    • 8a Yoshida H, Fukushimda H, Ohshita J, Kunai A. Angew. Chem. Int. Ed. 2004; 43: 3935
    • 8b Yoshida H, Fukushimda H, Ohshita J, Kunai A. Tetrahedron Lett. 2004; 45: 8659
    • 8c Yoshida H, Fukushima H, Morishita T, Ohshita J, Kunai A. Tetrahedron 2007; 63: 4793
  • 9 Allan KM, Gilmore CD, Stoltz BM. Angew. Chem. Int. Ed. 2011; 50: 4488
  • 10 Yoshida H, Asatsu Y, Mimura Y, Ito Y, Ohshita J, Takaki K. Angew. Chem. Int. Ed. 2011; 50: 9676
    • 11a Yoshida H, Fukushima H, Ohshita J, Kunai A. J. Am. Chem. Soc. 2006; 128: 11040
    • 11b Yoshida H, Morishita T, Ohshita J. Org. Lett. 2008; 10: 3845
  • 12 Sha F, Huang X. Angew. Chem. Int. Ed. 2009; 48: 3458
    • 13a Yoshioka E, Kohtani S, Miyabe H. Angew. Chem. Int. Ed. 2011; 50: 6638
    • 13b Yoshida H, Ito Y, Ohshita J. Chem. Commun. 2011; 47: 8512
  • 14 Yoshioka E, Tanaka H, Kohtani S, Miyabe H. Org. Lett. 2013; 15: 3938
    • 15a Jeganmohan M, Cheng C.-H. Chem. Commun. 2006; 2454
    • 15b Jeganmohan M, Bhuvaneswari S, Cheng C.-H. Chem. Asian J. 2010; 5: 153
    • 16a Nair V, Menon RS, Sreekanth AR, Abhilash B, Biju AT. Acc. Chem. Res. 2006; 39: 520
    • 16b Nair V, Rajesh C, Vinod AU, Bindu S, Sreekanth AR, Mathew JS, Balagopal L. Acc. Chem. Res. 2003; 36: 899
    • 17a Nair V, Pillai AN, Menon RS, Suresh E. Org. Lett. 2005; 7: 1189
    • 17b Nair V, Pillai AN, Beneesh PB, Suresh E. Org. Lett. 2005; 7: 4625
    • 17c Nair V, Sreekanth AR, Vinod AU. Org. Lett. 2001; 3: 3495
    • 17d Nair V, Sreekanth AR, Abhilash N, Biju AT, Devi BR, Menon RS, Rath NP, Srinivas R. Synthesis 2003; 1895
  • 18 While this manuscript was under review, Rodriguez, Coquerel et al. reported the resembling results on generation of 2-pyridylidenes from pyridine and arynes, and interception of these intermediates with isatin derivatives. For details, see: Nawaz F, Mohanan K, Charles L, Rajzmann M, Bonne D, Chuzel O, Rodriguez J, Coquerel Y. Chem. Eur. J. 2013; 19: 17578