메뉴 건너뛰기




Volumn 14, Issue 5, 2003, Pages 577-580

Alternative procedure for the synthesis of enantiopure 1-benzoyl-2(S)-tert-butyl-3-methylperhydropyrimidin-4-one, a useful starting material for the enantioselective synthesis of α-substituted β-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

1 BENZOYL 2 TERT BUTYL 3 METHYLPERHYDROPYRIMIDIN 4 ONE; AMINO ACID DERIVATIVE; ASPARAGINE; DIMETHYL SULFATE; HETEROCYCLIC COMPOUND; LEAD; PYRIMIDINE DERIVATIVE; TOXIC SUBSTANCE; UNCLASSIFIED DRUG;

EID: 0037424549     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(03)00048-X     Document Type: Article
Times cited : (19)

References (29)
  • 1
    • 0002497398 scopus 로고
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (1994) Aldrichim. Acta , vol.27 , pp. 3-11
    • Juaristi, E.1    Quintana, D.2    Escalante, J.3
  • 2
    • 0028130028 scopus 로고
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (1994) Tetrahedron , vol.50 , pp. 9517-9582
    • Cole, D.C.1
  • 3
    • 14844312173 scopus 로고    scopus 로고
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 117-128
    • Cardillo, G.1    Tomasini, C.2
  • 4
    • 0037201534 scopus 로고    scopus 로고
    • Wiley-VCH: New York
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (1997) Enantioselective Synthesis of β-Amino Acids
    • Juaristi, E.1
  • 5
    • 0345151817 scopus 로고    scopus 로고
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (1999) Curr. Med. Chem. , vol.6 , pp. 983-1004
    • Juaristi, E.1    López-Ruíz, H.2
  • 6
    • 0037201534 scopus 로고    scopus 로고
    • For reviews, see: (a) Juaristi, E.; Quintana, D.; Escalante, J. Aldrichim. Acta 1994, 27, 3-11; (b) Cole, D. C. Tetrahedron 1994, 50, 9517-9582; (c) Cardillo, G., Tomasini, C. Chem. Soc. Rev. 1996, 25, 117-128; (d) Enantioselective Synthesis of β-Amino Acids; Juaristi, E., Ed.; Wiley-VCH: New York, 1997; (e) Juaristi, E.; López-Ruíz, H. Curr. Med. Chem. 1999, 6, 983-1004; (f) Liu, M.; Sibi, M. P. Tetrahedron 2002, 58, 7991-8035.
    • (2002) Tetrahedron , vol.58 , pp. 7991-8035
    • Liu, M.1    Sibi, M.P.2
  • 25
    • 85026863964 scopus 로고
    • Decarboxylation can also be accomplished by electrolysis. See:
    • Decarboxylation can also be accomplished by electrolysis. See: Lakner F.J., Chu K.S., Negrete G.R., Konopelski J.P. Org. Synth. 73:1995;201-214.
    • (1995) Org. Synth. , vol.73 , pp. 201-214
    • Lakner, F.J.1    Chu, K.S.2    Negrete, G.R.3    Konopelski, J.P.4
  • 26
    • 33845605630 scopus 로고
    • For the hydrodehalogenation of α-haloketones with ITMS, see: (a) Olah, G. A.; Arvanaghi, M.; Dankar, Y. D. J. Org. Chem. 1980, 45, 3531-3532; (b) Ho, T.-L. Synth. Commun. 1981, 11, 101-103.
    • (1980) J. Org. Chem. , vol.45 , pp. 3531-3532
    • Olah, G.A.1    Arvanaghi, M.2    Dankar, Y.D.3
  • 27
    • 0001574284 scopus 로고
    • For the hydrodehalogenation of α-haloketones with ITMS, see: (a) Olah, G. A.; Arvanaghi, M.; Dankar, Y. D. J. Org. Chem. 1980, 45, 3531-3532; (b) Ho, T.-L. Synth. Commun. 1981, 11, 101-103.
    • (1981) Synth. Commun. , vol.11 , pp. 101-103
    • Ho, T.-L.1
  • 28
    • 37049146355 scopus 로고
    • Purchased from Aldrich or prepared according to:
    • Purchased from Aldrich or prepared according to: Pausacker K.H. J. Chem Soc. 1953;107-109.
    • (1953) J. Chem Soc. , pp. 107-109
    • Pausacker, K.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.