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Volumn 47, Issue 42, 2006, Pages 7417-7421

Direct organocatalytic asymmetric reductive Mannich-type reactions

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CATALYSIS; CHIRALITY; DIASTEREOISOMER; ENANTIOSELECTIVITY; MANNICH REACTION; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY;

EID: 33748434728     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.08.063     Document Type: Article
Times cited : (97)

References (57)
  • 36
    • 27544485685 scopus 로고    scopus 로고
    • For selected examples of organocatalytic asymmetric domino and cascade reactions see:
    • For selected examples of organocatalytic asymmetric domino and cascade reactions see:. Huang Y., Walji A.M., Larsen C.H., and MacMillan D.W.C. J. Am. Chem. Soc. 127 (2005) 15051
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 15051
    • Huang, Y.1    Walji, A.M.2    Larsen, C.H.3    MacMillan, D.W.C.4
  • 43
    • 7044235263 scopus 로고    scopus 로고
    • For an excellent review on domino reactions see:
    • For an excellent review on domino reactions see:. Tietze L.F. Chem. Rev. 96 (1996) 115
    • (1996) Chem. Rev. , vol.96 , pp. 115
    • Tietze, L.F.1
  • 48
    • 33748433592 scopus 로고    scopus 로고
    • note
    • 2O/pentane mixtures) to give 4.
  • 49
    • 33646905493 scopus 로고    scopus 로고
    • Both enantiomers of α,α-diphenylprolinol and α,α-di(2-naphthyl)prolinol are commercially available and TMS protected in one step. For the use of protected diarylprolinols in anti-selective Mannich type reactions see:
    • Both enantiomers of α,α-diphenylprolinol and α,α-di(2-naphthyl)prolinol are commercially available and TMS protected in one step. For the use of protected diarylprolinols in anti-selective Mannich type reactions see:. Ibrahem I., and Córdova A. Chem. Commun. (2006) 1760
    • (2006) Chem. Commun. , pp. 1760
    • Ibrahem, I.1    Córdova, A.2
  • 56
    • 33748425810 scopus 로고    scopus 로고
    • note
    • 3).
  • 57
    • 33748432334 scopus 로고    scopus 로고
    • note
    • 4. The solvent was removed and the crude product was purified by silica gel column chromatography (toluene/EtOAc = 20/1) to give a mixture of 5e (5:1, 55 mg, yield 80%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.