Corrigendum to "Organocatalyzed direct aldol condensation using l-proline and BINAM-prolinamides: regio-, diastereo-, and enantioselective controlled synthesis of 1,2-diols". [Tetrahedron: Asymmetry 17 (2006) 1027] (DOI:10.1016/j.tetasy.2006.03.023);Organocatalyzed direct aldol condensation using l-proline and BINAM-prolinamides: regio-, diastereo-, and enantioselective controlled synthesis of 1,2-diols

Tetrahedron Asymmetry

Volumn 17, Issue 7, 2006, Pages 1027-1031

  Guillena, Gabriela ^a   Hita, María del Carmen ^a   Nájera, Carmen ^a  

^a UNIVERSITY OF ALICANTE   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ALCOHOL DERIVATIVE; ALDEHYDE; AMIDE; DIMETHYL SULFOXIDE; GLYCOLIC ACID DERIVATIVE; PROLINE;

ALDOL REACTION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; ENANTIOSELECTIVITY; ISOMER; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 33646494852     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.04.004     Document Type: Erratum

References (44)

1. Rychnovsky S.D. Chem. Rev. 95 (1995) 2021-2040
2. In: Wang P.G., and Bertozzi C. (Eds). Glycochemistry: Principles, Synthesis and Applications (2001), Marcel Dekker, New York
3. In: Omura S. (Ed). Macrolide Antibiotics: Chemistry, Biochemistry and Practice (2002), Academic Press, London
4. For general reviews on the catalytic enantioselective aldol reaction:. Gröger H., Vogl E.M., and Shibasaki M. Chem. Eur. J. 4 (1998) 1137-1141
5. Nelson S.G. Tetrahedron: Asymmetry 9 (1998) 357-389
6. Carreira E.M. In: Jacobsen E.N., Platz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis Vol. 3 (1999), Springer, Heidelberg Chapter 29-188
7. Mahrwald R. Chem. Rev. 96 (1999) 1095-1120
8. Machajewski T.D., and Wong C.-H. Angew. Chem., Int. Ed. 39 (2000) 1352-1374
9. Alcaide B., and Almendros P. Eur. J. Org. Chem. (2002) 1595-1601
10. In: Marhrwald R. (Ed). Modern Aldol Reactions Vols. 1-2 (2004), Wiley-VCH, Weinheim
11. Palomo C., Oiarbide M., and García J.M. Chem. Rev. Soc. 33 (2004) 65-75
12. Mestres R. Green Chem. 6 (2004) 583-603
13. Wong C.-H., and Whitesides G. Enzymes in Synthetic Organic Chemistry (1994), Pergamon Press, Oxford
14. Gijsen H.J.M., Qiao L., Fitz W., and Wong C.-H. Chem. Rev. 96 (1996) 443-474
15. Tanaka F., and Barbas III C.F. In: Marhrwald R. (Ed). Modern Aldol Reactions Vol. 1 (2004), Wiley-VCH, Weinheim Chapter 6
16. Yamada Y.M.A., Yoshikawa N., Sasai H., and Shibasaki M. Angew. Chem., Int. Ed. 36 (1997) 1871-1873
17. Yoshikawa N., Yamada Y.M.A., Das J., Sasai H., and Shibasaki M. J. Am. Chem. Soc. 121 (1999) 4168-4178
18. Trost B.M., and Ito H. J. Am. Chem. Soc. 122 (2000) 12003-12004
19. Yoshikawa N., Kumagai N., Matsunaga S., Moll G., Ohshima T., Suzuki T., and Shibasaki M. J. Am. Chem. Soc. 123 (2001) 2466-2467
20. Trost B.M., Ito H., and Silcoff E.R. J. Am. Chem. Soc. 123 (2001) 3367-3368
21. For recent reviews concerning the use of organocatalysts in asymmetric aldol reactions, see:. List B. Acc. Chem. Res. 37 (2004) 548-557
22. Saito S., and Yamamoto H. Acc. Chem. Res. 37 (2004) 570-579
23. Notz W., Tanaka F., and Barbas III C.F. Acc. Chem. Res. 37 (2004) 580-591
24. Allemann C., Gordillo R., Clemente F.R., Cheong P.H.-Y., and Houk K.N. Acc. Chem. Res. 37 (2004) 558-569
25. Pihko P.M. Angew. Chem., Int. Ed. 43 (2004) 2062-2064
26. Kazmaier U. Angew. Chem., Int. Ed. 44 (2005) 2186-2188
27. Limbach M. Chem. Biol. 2 (2005) 825-836
28. Berkessel A., and Groger H. Asymmetric Organocatalysts (2005), Wiley-VCH, Weinheim
29. Special Issue: Organocatalysis in Organic Synthesis. Tetrahedron 62 (2006) 243-502
30. For an excellent review about the use of α-hydroxyacetone derivatives in organic synthesis, see:. Enders D., Voith M., and Lenzen A. Angew. Chem., Int. Ed. 44 (2005) 1304-1325
31. List B., Shabat D., Barbas III C.F., and Lerner R.A. Chem. Eur. J. 4 (1998) 881-885
32. Shabat D., List B., Lerner R.A., and Barbas III C.F. Tetrahedron Lett. 40 (1999) 1437-1440
33. Maggiotti V., Resmini M., and Gouverneur V. Angew. Chem., Int. Ed. 41 (2002) 1012-1014
34. List B., Lerner R.A., and Barbas III C.F. J. Am. Chem. Soc. 122 (2000) 2395-2396
35. Notz W., and List B. J. Am. Chem. Soc. 122 (2000) 7386
36. Pan Q., Zou B., Wang Y., and Ma D. Org. Lett. 6 (2004) 1009-1012
37. Tang Z., Yang Z.-H., Cun L.-F., Gong L.-Z., Mi A.-Q., and Jiang Y.-Z. Org. Lett. 6 (2004) 2285-2287
38. Guillena G., Hita M.C., and Nájera C. Tetrahedron: Asymmetry 17 (2006) 729-733
39. Baker-Glenn C., Ancliff R., and Gouverneur V. Tetrahedron 60 (2004) 7607-7619
40. Zou W., Ibrahem I., Dziedzic P., Sundén H., and Cordóva A. Chem. Commun. (2002) 3024-3025
41. Cordóva A., Notz W., and Barbas III C.F. Chem. Commun. (2005) 4946-4948
42. Nyberg A.I., Usano A., and Pihko P.M. Synlett (2004) 1891-1896
43. Liu H., Peng L., and Li Y. New. J. Chem. 27 (2003) 1159-1160
44. 17 for the same reaction conditions being anti:syn:iso ratio of 90:7:3 with 90% and 15% ee for the anti and syn diastereomers, respectively.