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Volumn 6, Issue 24, 2004, Pages 4423-4426

CamTHP*OH: A camphor-derived δ-lactol auxiliary for the effective desymmetrization of attached glycinamide residues. Asymmetric synthesis of α-amino carbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; CAMPHOR DERIVATIVE; CARBONYL DERIVATIVE; GLYCINAMIDE; ORGANOLITHIUM COMPOUND; REAGENT;

EID: 10044248824     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol048569i     Document Type: Article
Times cited : (19)

References (34)
  • 22
    • 0028355337 scopus 로고
    • For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
    • (1994) Tetrahedron , vol.50 , pp. 1539
    • Duthaler, R.O.1
  • 23
    • 0001313865 scopus 로고
    • For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 299
    • Hegedus, L.1
  • 24
    • 0038106171 scopus 로고    scopus 로고
    • For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
    • (1998) Chem. Rev. , vol.98 , pp. 1407
    • Bloch, R.1
  • 25
    • 0033043246 scopus 로고    scopus 로고
    • For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
    • (1999) Amino Acids , vol.16 , pp. 215
    • Calmes, M.1    Daunis, J.2
  • 26
    • 0141869057 scopus 로고    scopus 로고
    • For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4290
    • Ma, J.-A.1
  • 31
    • 10044228995 scopus 로고    scopus 로고
    • note
    • 3).
  • 32
    • 0037844251 scopus 로고    scopus 로고
    • For related examples using other N-carbamate-protected α-amino amides, see: (a) Nájera, C.; Abellán, T.; Sansano, J. M. Eur. J. Org. Chem. 2000, 2809. (b) Sengupta, S.; Mondal, S.; Das, D. Tetrahedron Lett. 1999, 40, 4107.
    • (2000) Eur. J. Org. Chem. , pp. 2809
    • Nájera, C.1    Abellán, T.2    Sansano, J.M.3
  • 33
    • 0033591193 scopus 로고    scopus 로고
    • For related examples using other N-carbamate-protected α-amino amides, see: (a) Nájera, C.; Abellán, T.; Sansano, J. M. Eur. J. Org. Chem. 2000, 2809. (b) Sengupta, S.; Mondal, S.; Das, D. Tetrahedron Lett. 1999, 40, 4107.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 4107
    • Sengupta, S.1    Mondal, S.2    Das, D.3
  • 34
    • 10044244274 scopus 로고    scopus 로고
    • note
    • Compound 22 was available in one step from commercial N-Cbz-L-phenylalanine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.