4
Tetrahedron Letters
(h) Farrell JR, Niconchuk J, Higham CS, Bergeron BW.
Tetrahedron Lett. 2007; 48: 8034;
paraformaldehyde and amines for the synthesis of Mannich
bases and benzoxazines in one pot. The present work making use
of the stable and wide commercial available arylboronic acids as
the starting materials provides a new route for the synthesis of
Mannich bases and benzoxazines.
(i) Omura Y, Taruno Y, Irisa Y, Morimoto M, Saimotoa H,
Shigemasa Y. Tetrahedron Lett. 2001; 42: 7273;
(j) Anwar HF, Skattebølb L, Hansen TV. Tetrahedron. 2007; 63:
9997;
(k) Szatmári I, Fülöp F. Tetrahedron. 2013; 69: 1255;
(l) Rivera A, Quevedo R. Tetrahedron Lett. 2013; 54: 1416;
(m) Habata Y, Akabori S. Ind Eng Chem Res. 2000; 39: 3465.
(n) Chi KW, Ahn YS, Shim KT, Park TH, Ahn JS. Bull Korean
Chem Soc. 1999; 20: 973;
Acknowledgments
This work was supported by the National Key Research and
Development Program of China (2016YFA0602900) and the
National Natural Science Foundation of China (21572070).
(o) Hellmann H, Opitz G. Angew Chem. 1956; 68: 265;
(p) Kuriakose AP. Indian J Chem. 1975; 13: 1149;
(q) Monti SA, Johnson WO. Tetrahedron. 1970; 26: 3685.
13. Takahashi H, Kashiwa N, Hashimoto Y, Nagasawa K.
Tetrahedron Lett. 2002; 43: 2935.
References and notes
1. Chadwick J, Amewu RK, Marti F, Garah FBE, Sharma R, Berry N
G, Stocks PA, Saward HB, Wittlin S, Rottmann M, Brun R,
Taramelli D, Parapini S, Ward SA, O’Neil PM. ChemMedChem.
2011; 6: 1357.
2. Aytemira MD, Çalış Ü, Özalp M. Arch Pharm Pharm Med Chem.
2004; 337: 281.
3. (a) Ooi T, Maruoka K. Angew Chem Int Ed. 2007; 46: 4222;
(b) Graaff CD, Ruijte E, Orru RVA. Chem Soc Rev. 2012; 41:
3969;
Supplementary Material
Supplementary material that may be helpful in the review
process should be prepared and provided as a separate electronic
file. That file can then be transformed into PDF format and
submitted along with the manuscript and graphic files to the
appropriate editorial office.
(c) Kobayashi S, Ishitani H. Chem Rev. 1999; 99: 1069;
(d) Hamada T, Manabe K, Kobayashi S. J Am Chem Soc. 2004;
126: 7768;
(e) Guo QX, Liu H, Guo C, Luo SW, Gu Y, Gong LZ. J Am Chem
Soc. 2007; 129: 3790.
4. Water RWVD, Pettus TRR. Tetrahedron. 2002; 58: 5367.
5. Oie H, Sudo A, Endo T. J Poly Sci: Part A: Poly Chem. 2010; 48:
5357.
6. (a) Tramontini M, Angiolini L. Tetrahedron. 1990; 46: 1791;
(b) Hwang DR, Uang BJ. Org Lett. 2002; 4: 463;
(c) Cheng LL, Han X, Huang HM, Wong MW, Lu YX. Chem
Commun. 2007; 39: 4143;
(d) Assimomytis N, Sariyannis Y, Stavropoulos G, Tsoungas PG,
Varvounis G, Cordopatis P. Synlett. 2009; 41: 2777;
(e) Takahashi H, Kashiwa N, Hashimoto Y, Nagasawa K.
Tetrahedron Lett. 2002; 43: 2935;
(f) Speckamp WN, Moolenaar MJ. Tetrahedron. 2000; 56: 3817;
(g) Bur SK, Martin SF, Tetrahedron. 2001; 57: 3221;
(h) Trost BM, Terrell LR. J Am Chem Soc. 2003; 125: 338;
(i) Rodríguez B, Bolm C. J Org Chem. 2006; 71: 2888.
7. Chang T, He LQ, Bian L, Han HY, Yuan MX, Gao XR. RSC Adv.
2014; 4: 727.
8. Chen WJ, Seidel D. Org Lett. 2014; 16: 3158.
9. Zhang YX, Han JW, Liu ZJ. RSC Adv. 2015; 5: 25485.
10. (a) Candeias NR, Montalbano F, Cal PMSD, Gois PMP. Chem
Rev. 2010; 110: 6169;
(b) Zhu C, Wang R, Falck JR. Org Lett. 2012; 14: 3494;
(c) Prakash GKS, Chacko S, Panja C, Thomas TE, Gurung L,
Rasul G, Mathew T, Olah GA. Adv Synth Catal 2009; 351: 1567;
(d) Hosoi K, Kuriyama Y, Inagi S, Fuchigami T. Chem Commun.
2010; 46: 1284;
(e) Gohain M, Plessis MD, Tonder JHV, Bezuidenhoudt BCB.
Tetrahedron Lett. 2014; 55: 2082.
11. (a) Zou YQ, Chen JR, Liu XP, Lu LQ, Davis RL, Jørgensen KA,
Xiao WJ. Angew Chem Int Ed. 2012; 51: 784;
(b) Gupta S, Chaudhary P, Seva L, Sabiahb S, Kandasamy J. RSC
Adv. 2015; 5: 89133;
(c) Gogoi P, Bezboruah P, Gogoi J, Boruah RC. Eur J Org Chem.
2013; 2013: 7291;
(d) Mulakayala N, Ismail, Kumar KM, Rapolu RK, Kandagatla B,
Rao P, Oruganti S, Pal M. Tetrahedron Lett. 2012; 53: 6004.
12. (a) Burke WJ. J Am Chem Soc. 1949; 71: 609;
(b) Zhang Q, Yang P, Deng YY, Zhang CX, Zhu RQ, Gu Y. RSC
Adv. 2015; 5: 103203;
(c) Burke WJ, Murdock KC, Ec G. J Am Chem Soc. 1954; 76:
1677;
(d) Imran M, Kiskan B, Yagci Y. Tetrahedron Lett. 2013; 54:
4966;
(e) Zhao LM, Zhang LM, Ma FY, Wang XS, Jin HS. Tetrahedron
Lett. 2013; 54: 2802;
(f) Mulla SAR, Salama TA, Pathan MY, Inamdar SM, Chavan SS.
Tetrahedron Lett. 2013; 54: 672;
(g) Karmakar B, Banerji J. Tetrahedron Lett. 2011; 52: 4957;