메뉴 건너뛰기




Volumn , Issue , 2008, Pages 185-205

Direct Catalytic Asymmetric Mannich Reactions and Surroundings

Author keywords

Amino group chemistry; Direct catalytic asymmetric mannich reactions; Metal free organocatalysis; Organometallic Catalysts; Surroundings

Indexed keywords


EID: 69249191119     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527621262.ch5     Document Type: Chapter
Times cited : (7)

References (117)
  • 1
    • 37049166036 scopus 로고
    • The first example of the application of the Mannich reaction to natural product synthesis is attributed to Robinson in his synthesis of tropinone;
    • The first example of the application of the Mannich reaction to natural product synthesis is attributed to Robinson in his synthesis of tropinone; R. Robinson, J. Chem. Soc. 1917, 762.
    • (1917) J. Chem. Soc. , pp. 762
    • Robinson, R.1
  • 2
    • 0000733768 scopus 로고
    • Comprehensive Organic Synthesis;
    • For excellent reviews, see:, in, B. M. Trost, I. Flemming, Eds.; Pergamon Press: New York, , Chapter 4.1.
    • For excellent reviews, see: E. F. Kleinmann, in Comprehensive Organic Synthesis; B. M. Trost, I. Flemming, Eds.; Pergamon Press: New York, 1991; Vol. 2, Chapter 4.1.
    • (1991) , vol.2
    • Kleinmann, E.F.1
  • 5
    • 0002927738 scopus 로고    scopus 로고
    • Comprehensive Asymmetric Catalysis;
    • in, E. N. Jacobsen, A. Pfaltz, H. Yamomoto, Eds.; Springer: Berlin
    • S. Denmark, O. J.-C. Nicaise, in Comprehensive Asymmetric Catalysis; E. N. Jacobsen, A. Pfaltz, H. Yamomoto, Eds.; Springer: Berlin, 1999, Vol. 2, 93.
    • (1999) , vol.2 , pp. 93
    • Denmark, S.1    Nicaise, O.J.-C.2
  • 6
    • 0003693460 scopus 로고    scopus 로고
    • Enantioselective Synthesis of ß-Amino Acids
    • For examples, see:, E. Juaristi, Ed., Wiley-VCH, Weinheim
    • For examples, see: Enantioselective Synthesis of ß-Amino Acids, E. Juaristi, Ed., Wiley-VCH, Weinheim, 1997.
    • (1997)
  • 9
    • 0002846446 scopus 로고
    • Topics in Current Chemistry
    • in, F. L. Boschke, Ed., Springer Verlag, Berlin
    • U. Schöllkopf, in Topics in Current Chemistry, F. L. Boschke, Ed., Springer Verlag, Berlin, 1983, Vol. 109, pp 45-85
    • (1983) , vol.109 , pp. 45-85
    • Schöllkopf, U.1
  • 23
  • 42
    • 0033936085 scopus 로고    scopus 로고
    • 2-bisoxazoline-Lewis acid complexes see:
    • 2-bisoxazoline-Lewis acid complexes see: J. S. Johnson, D. A. Evans, Acc. Chem. Res. 2000, 33, 325.
    • (2000) Acc. Chem. Res. , vol.33 , pp. 325
    • Johnson, J.S.1    Evans, D.A.2
  • 51
    • 33845519609 scopus 로고
    • Asymmetric Synthesis of Optically Active Polycyclic Organic Compounds
    • German Patent. D. E. 2102623, Jul 29
    • Z. G. Hajos, D. R. Parrish, Asymmetric Synthesis of Optically Active Polycyclic Organic Compounds. German Patent. D. E. 2102623, Jul 29, 1971.
    • (1971)
    • Hajos, Z.G.1    Parrish, D.R.2
  • 53
    • 52149116641 scopus 로고
    • Optically Active 1, 5-Indanone and 1, 6-Naphthalenedionene
    • German Patent DE 2014757, Oct 7
    • U. Eder, G. Sauer, R. Wiechert, Optically Active 1, 5-Indanone and 1, 6-Naphthalenedionene. German Patent DE 2014757, Oct 7, 1971.
    • (1971)
    • Eder, U.1    Sauer, G.2    Wiechert, R.3
  • 56
    • 11044223276 scopus 로고    scopus 로고
    • For example, the total synthesis of taxol:
    • For example, the total synthesis of taxol: S. J. Danishefsky, et al. J. Am. Chem. Soc. 1996, 118, 2843.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 2843
    • Danishefsky, S.J.1
  • 61
    • 0001549125 scopus 로고    scopus 로고
    • and references therein.
    • K. Manabe, S. Kobayashi, Org. Lett. 1999, I, 1965. and references therein.
    • (1999) Org. Lett. , vol.I , pp. 1965
    • Manabe, K.1    Kobayashi, S.2
  • 82
    • 84891322432 scopus 로고    scopus 로고
    • 225th ACS National Meeting, New Orleans, LA. Amine-Catalyzed Direct Asymmetric Mannichtype Reactions: Enantioselective Synthesis of Amino Acid and Amino Alcohol Derivatives
    • A. Córdova, 225th ACS National Meeting, New Orleans, LA. Amine-Catalyzed Direct Asymmetric Mannichtype Reactions: Enantioselective Synthesis of Amino Acid and Amino Alcohol Derivatives.
    • Córdova, A.1
  • 86
    • 84891283528 scopus 로고    scopus 로고
    • The Mannich adducts are reduced to the more stabile γ-amino alcohols prior to isolation and ee determination, due to their lower risk of decomposition, epimerization and racemization.
    • The Mannich adducts are reduced to the more stabile γ-amino alcohols prior to isolation and ee determination, due to their lower risk of decomposition, epimerization and racemization.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.