Erratum: A catalytic and enantioselective synthesis of trans-2-amino-1- aryltetralins (Advanced Synthesis and Catalysis (2009) 6 (859-864) DOI: 10.1002/adsc.200800603);A catalytic and enantioselective synthesis of trans-2-amino-1-aryltetralins

Advanced Synthesis and Catalysis

Volumn 351, Issue 6, 2009, Pages 859-864

  Hajra, Saumen ^a   Maji, Biswajit ^a   Mal, Dipakranjan ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

Author keywords

2 Amino 1 aryltetralins; Aziridination; Catalytic synthesis; Enantioselectivity; Friedel Crafts alkylation; 2 amino 1 aryltetralins; aziridination; catalytic synthesis; enantioselectivity

Indexed keywords

EID: 65349097522     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.201090036     Document Type: Erratum

References (30)

1. a) S. Peter, I. Ruben, K. Bjorn, CMS Drug Rev. 2004, 10, 230-242;
2. b) W. J. Giardina, M. Williams, CNS Drug Rev. 2001, 7, 305-316.
3. a) W.K. Brewster, D. E. Nichols, R. M. Riggs, D. M. Mottola, T. W. Lovenberg, M. H. Lewis, R. B. Mailman, J. Med. Chem. 1990, 33, 1756-1764;
4. b) J. R. Taylor, M. S. Lawrence, D. E. Redmont, J. D. Elsworth, R. H. Roth, D. E. Nochols, R. B. Mailman, Eur. J. Pharmacol. 1991, 199, 389-391;
5. c) M. P. Seiler, A. Hagenbach, H.-J. Wüthrich, R. Marksteun, J. Med. Chem. 1991, 34, 303-307;
6. d) T. A, Knoerzer, D. E. Nichols, W. K. Brewster, V. J. Watts, D. Mottola, R. B. Mailman, J. Med. Chem. 1994, 37, 2453-2460;
7. e) M. R. Michaelides, Y. Hong Jr., S. DiDomenico, K. E. Asin, D. R. Britton, C. W. Lin, M. Williams, K. Shiosaki, J. Med. Chem. 1995, 38, 3445-3447.
8. P. P. Ehrlich, J. W. Ralston, M. R. Michaelides, J. Org. Chem. 1997, 62, 2782-2785.
9. a) M. Yamashita, K.-I. Yamada, K. Tomioka, J. Am. Chem. Soc. 2004, 126, 1954-1955;
10. b) M. Yamashita, K.- I. Yamada, K. Tomioka, Tetrahedron 2004, 60, 4237-4242;
11. c) Y. Asano, M. Yamashita, K, Nagai, M. Kuriya-ma, K.-I. Yamada, K. Tomioka, Tetrahedron Lett. 2001, 42, 8493-8495.
12. a) W. H. Pearson, B. W. Lian, S. C. Bergmeier, in: Comprehensive Heterocyclic Chemistry II, 2nd edn., (Ed.; A. Padwa), Pergamon, Oxford, 1996, Vol. 1 A, pp 1-60;
13. b) K. M. Lokanatha Rai, A. Hassner, in: Comprehensive Heterocyclic Chemistry II, 2nd edn., (Ed.: A. Padwa), Pergamon, Oxford, 1996, Vol. 1A, pp 61-96; for recent reviews, see:
14. c) X. E. Hu, Tetrahedron 2004, 60, 2701-2743;
15. d) W. McCoull, F. A. Davis, Synthesis 2000, 1347-1365;
16. e) R. S. Atkinson, Tetrahedron 1999, 55, 1519-1559;
17. f) D. Tanner, Angew. Chem. 1994, 106, 625-646;
18. Angew. Chem. Int. Ed. Engl. 1994, 33, 599-619.
19. Intra- and intermolecular aziridne ring opening by π-nucleophiles for racemic mixtures: a) S. C. Bergmeier, S. Katz, J. Huang, H. McPherson, P. J. Donoghue, D. D. Reed, Tetrahedron Lett. 2004, 45, 5011-5014;
20. b) S. Roy, M. Bera, Tetrahedron Lett. 2007, 48, 7144-7146;
21. c) J. S. Yadav, B. V. S. Reddy, R. S. Rao, G. Veerendhar, K. Nagaiah, Tetrahedron Lett. 2001, 42, 8067-8070.
22. S. Hajra, B. Maji, D. Sinha, S. Bar, Tetrahedron Lett. 2008, 49, 4057-4059.
23. For recent reviews on asymmetric aziridination, see: a) P. Muller, C. Fruit, Chem. Rev. 2003, 103, 2905-2919;
24. b) H. M. I. Osborn, J. Sweeny, Tetrahedron: Asymmetry 1997, 8, 1693-1715.
25. D. A, Evans, M. M. Faul, M. T. Bilodeau, B. A. Anderson, D. M. Barnes, J. Am. Chem. Soc. 1993, 115, 5328-5329.
26. The formation of a mixture of cis- and trans-aziridines from pure cis-alkenes is known in literature: P. Brandt, M. J. Sdergren, P. G. Andesson, P.-O. Norrby J. Am. Chem, Soc. 2000, 122, 8013-8020.
27. M.K. Ghorai, K. Das, D. Shukla J. Org. Chem. 2007, 72, 5859-5862.
28. I. Ungureanu, P. Koltz, A. Mann Angew. Chem. 2000, 112, 4790-4792;
29. Angew. Chem. Int. Ed. 2000, 39, 4615-4617.
30. R. Narayan, M. VanNieuwenhze Org. Lett. 2005, 7, 2655-2658.