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Synthesis 2016; 48(16): 2645-2652
DOI: 10.1055/s-0035-1562486
DOI: 10.1055/s-0035-1562486
special topic
Asymmetric Synthesis of Methylphenidate and Quinolizidinones by Addition of Aldehydes to Piperidine-Based Conjugated N-Acyliminium Ions
Further Information
Publication History
Received: 13 April 2016
Accepted after revision: 18 May 2016
Publication Date:
24 June 2016 (online)
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Dedicated to Prof. Paolo Crotti on the occasion of his 70th birthday
Abstract
The synergistic effect of Lewis acids and MacMillan organocatalyst allows the α-regioselective and enantioselective α-amidoalkylation of piperidine derivatives with enolizable aldehydes. The potentiality of the synthetic method is illustrated by a short asymmetric synthesis of the eutomer of the blockbuster drug Ritalin and by a concise formal synthesis of 1-alkyl-4-substituted quinolizidine alkaloids.
Key words
conjugated acyliminium - organocatalysis - asymmetric synthesis - α-amidoalkylation - aldehydes - tetrahydropyridines - quinolizidine alkaloidsSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1562486.
- Supporting Information
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References
- 1a Laschat S, Dickner T. Synthesis 2000; 1781
- 1b Felpin F.-X, Lebreton J. Eur. J. Org. Chem. 2003; 3693
- 1c Escolano C, Amat M, Bosch J. Chem. Eur. J. 2006; 12: 8198
- 1d Bull JA, Mousseau JJ, Pelletier G, Charette AB. Chem. Rev. 2012; 112: 2642
- 2a Santos LS, Mirabal-Gallardo Y, Shankaraiah N, Simirgiotis MJ. Synthesis 2011; 51
- 2b Han P, Si C.-M, Mao Z.-Y, Li H.-T, Wei B.-G, Du Z.-T. Tetrahedron 2016; 72: 862 ; and pertinent references cited therein
- 3a Liu X, Meng Z, Li C, Lou H, Liu L. Angew. Chem. Int. Ed. 2015; 54: 6012
- 3b Ichikawa E, Suzuki M, Yabu K, Albert M, Kanai M, Shibasaki M. J. Am. Chem. Soc. 2004; 126: 11808
- 3c Myers EL, de Vries JG, Aggarwal VK. Angew. Chem. Int. Ed. 2007; 46: 1893
- 3d Sun Z, Yu S, Ding Z, Da M. J. Am. Chem. Soc. 2007; 129: 9300
- 3e Black DA, Beveridge RE, Arndtsen BA. J. Org. Chem. 2008; 73: 1906
- 3f Fernández-Ibáñez MA, Maciá B, Pizzuti MG, Minnaard AJ, Feringa BL. Angew. Chem. Int. Ed. 2009; 48: 9339
- 3g Nadeau C, Aly S, Belyk K. J. Am. Chem. Soc. 2011; 133: 2878
- 3h Chau ST, Lutz JP, Wu K, Doyle AG. Angew. Chem. Int. Ed. 2013; 52: 9153
- 3i Shi S.-L, Wei XF, Shimizu Y, Kanai M. J. Am. Chem. Soc. 2012; 134: 17019
- 4a Mengozzi L, Gualandi A, Cozzi PG. Chem. Sci. 2014; 5: 3915
- 4b Gualandi A, Mengozzi L, Manoni E, Cozzi PG. Catal. Lett. 2015; 145: 398
- 5a Sun S, Mao Y, Lou H, Liu L. Chem. Commun. 2015; 51: 10691
- 5b Berti F, Malossi F, Marchetti F, Pineschi M. Chem. Commun. 2015; 51: 13694
- 5c Volla CM. R, Fava E, Atodiresei I, Rueping M. Chem. Commun. 2015; 51: 15788
- 6 For an intramolecular version, see: Koley D, Krishna Y, Srinivas K, Khan AA, Kant R. Angew. Chem. Int. Ed. 2014; 53: 13196
- 7 Yazici A, Wille U, Pyne SG. J. Org. Chem. 2016; 81: 1434 ; and pertinent references cited therein
- 8a Matsumura Y, Kanda Y, Shirai K, Onomura O, Maki T. Tetrahedron 2000; 692: 654
- 8b Matsumura Y, Minato D, Onomura O. J. Organomet. Chem. 2007; 56: 7411
- 9a Kozikowski AP, Park P.-u. J. Org. Chem. 1984; 49: 1674
- 9b Torii S, Inokuchi T, Takagishi S, Akaoshi F, Uneyama K. Chem. Lett. 1987; 639
- 10a Davies HM. L, Hansen T, Hopper DW, Panaro SA. J. Am. Chem. Soc. 1999; 121: 6509
- 10b Axten JM, Ivy R, Krim L, Winkler JD. J. Am. Chem. Soc. 1999; 121: 6511
- 11 Sebesta R, Pizzuti MG, Boersma AJ, Minnaard AJ, Feringa BL. Chem. Commun. 2005; 1711
- 12 Prashad M, Kim H.-Y, Lu Y, Liu Y, Har D, Repic O, Blacklock TJ, Giannousis P. J. Org. Chem. 1999; 64: 1750
- 13 Ma S, Ni B. Chem. Eur. J. 2004; 10: 3286
- 14a Daly JW, Spande TF, Garraffo HM. J. Nat. Prod. 2005; 68: 1556
- 14b Michael JP In The Alkaloids . Vol. 75. Knölker H.-J. Elsevier Academic Press; London: 2016: 1
- 15a Moorthy NV. G, Dyapa R, Pansare SV. Org. Lett. 2015; 17: 5312
- 15b Kauloorkar SV, Jha V, Kumar P. RSC Adv. 2013; 3: 18288
- 15c Veerasamy N, Carlson EC, Collett ND, Saha M, Carter RG. J. Org. Chem. 2013; 78: 4779
- 15d Pham HT, Chataigner I, Renaud J.-L. Curr. Org. Chem. 2012; 16: 1754
- 15e Pansare SV, Dyapa R. Org. Biomol. Chem. 2012; 10: 6776
- 15f Fustero S, Moscardó J, Sánchez-Roselló M, Flores S, Guerola M, del Pozo C. Tetrahedron 2011; 67: 7412
- 15g Yang H, Carter RG. J. Org. Chem. 2010; 75: 4929
- 15h Zhang W, Franzen J. Adv. Synth. Catal. 2010; 352: 499
- 15i Verkade JM. M, van der Pijl F, Willems MM. J. H. P, Quaedflieg PJ. L. M, van Delft FL, Rutjes FP. J. T. J. Org. Chem. 2009; 74: 3207
- 15j Franzen J, Fisher A. Angew. Chem. Int. Ed. 2009; 48: 787
- 15k Nishikawa Y, Kitajima M, Kogure N, Takayama H. Tetrahedron 2009; 65: 1608
- 16a Amat M, Semak V, Escolano C, Molins E, Bosch J. Org. Biomol. Chem. 2012; 10: 6866
- 16b Kinderman SS, De Gelder R, Van Maarseveen JH, Schoemaker HE, Hiemstra H, Rutjes FP. J. T. J. Am. Chem. Soc. 2004; 126: 4100
- 17 Lindemann C, Schneider C. Synthesis 2016; 48: 828
- 18 Tsukano C, Oimura A, Enkhtaivan I, Takemoto Y. Org. Lett. 2012; 14: 1902
- 19 Fellah M, Santarem M, Lhommet G, Mouriès-Mansuy VJ. Org. Chem. 2010; 75: 7803
- 20 Hodgson DM, Miles TJ, Witherington J. Tetrahedron 2003; 59: 9729
- 21 Thai DL, Sapko MT, Reiter CT, Bierer DE, Perel JM. J. Med. Chem. 1998; 41: 591
For selected reviews, see:
For reviews, see: