메뉴 건너뛰기




Volumn 15, Issue 3, 2004, Pages 525-535

Synthesis of atropisomeric 2,8-dioxygenated N,N-diisopropyl-1-naphthamides via kinetic resolution under Sharpless asymmetric dihydroxylation conditions

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; N,N DIISOPROPYL 2 (2' BUTENOYLOXY) 8 METHOXY 1 NAPHTHAMIDE; UNCLASSIFIED DRUG;

EID: 0742306890     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.11.039     Document Type: Article
Times cited : (25)

References (65)
  • 13
    • 0033525694 scopus 로고    scopus 로고
    • (Corrigendum: Fujita, M., Kitagawa, O., Izawa, H., Dobashia, A., Fukaya, H., Taguchi, T. Tetrahedron Lett. 2000, 41, 4997)
    • Fujita M., Kitagawa O., Izawa H., Dobashia A., Fukaya H., Taguchi T. Tetrahedron Lett. 40:1999;1949-1952. (Corrigendum: Fujita, M., Kitagawa, O., Izawa, H., Dobashia, A., Fukaya, H., Taguchi, T. Tetrahedron Lett. 2000, 41, 4997).
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1949-1952
    • Fujita, M.1    Kitagawa, O.2    Izawa, H.3    Dobashia, A.4    Fukaya, H.5    Taguchi, T.6
  • 23
    • 0033617110 scopus 로고    scopus 로고
    • Selected examples of axially chiral N-arylimides, see:
    • Selected examples of axially chiral N-arylimides, see: Curran D.P., Geib S., DeMello N. Tetrahedron. 55:1999;5681-5704.
    • (1999) Tetrahedron , vol.55 , pp. 5681-5704
    • Curran, D.P.1    Geib, S.2    Demello, N.3
  • 26
    • 0032556515 scopus 로고    scopus 로고
    • Selected examples of axially chiral benzamides, see:
    • Selected examples of axially chiral benzamides, see: Koide H., Uemura M. Chem. Commun. 1998;2483-2484.
    • (1998) Chem. Commun. , pp. 2483-2484
    • Koide, H.1    Uemura, M.2
  • 31
    • 0029935516 scopus 로고    scopus 로고
    • Selected examples of axially chiral 1-naphthamides, see:
    • Selected examples of axially chiral 1-naphthamides, see: Thayumanavan S., Beak P., Curran D.P. Tetrahedron Lett. 37:1996;2899-2902.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2899-2902
    • Thayumanavan, S.1    Beak, P.2    Curran, D.P.3
  • 32
    • 0002046801 scopus 로고    scopus 로고
    • and references cited therein
    • Clayden J. Synlett. 5:1998;810-816. and references cited therein.
    • (1998) Synlett , vol.5 , pp. 810-816
    • Clayden, J.1
  • 41
    • 0345022255 scopus 로고
    • Atropisomeric naphthalene derivatives possessing a vinyl group at C1, see:
    • Atropisomeric naphthalene derivatives possessing a vinyl group at C1, see: Kawabata T., Yahiro K., Fuji K. J. Am. Chem. Soc. 113:1991;9694-9696.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9694-9696
    • Kawabata, T.1    Yahiro, K.2    Fuji, K.3
  • 43
    • 0032171318 scopus 로고    scopus 로고
    • Atropisomeric naphthalene derivatives possessing an arylsulfinyl group at C1, see:
    • Atropisomeric naphthalene derivatives possessing an arylsulfinyl group at C1, see: Hiroi K., Suzuki Y. Tetrahedron Lett. 39:1998;6499-6502.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6499-6502
    • Hiroi, K.1    Suzuki, Y.2
  • 55
    • 0037019649 scopus 로고    scopus 로고
    • A recent example of kinetic resolution on atropisomeric amides under Sharpless asymmetric dihydroxylation conditions, see:
    • A recent example of kinetic resolution on atropisomeric amides under Sharpless asymmetric dihydroxylation conditions, see: Rios R., Jimeno C., Carroll P.J., Walsh P.J. J. Am. Chem. Soc. 124:2002;10272-10273.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10272-10273
    • Rios, R.1    Jimeno, C.2    Carroll, P.J.3    Walsh, P.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.