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Volumn 63, Issue 19, 1998, Pages 6472-6475

N-alkoxy analogues of 3,4,5-trihydroxypiperidine

Author keywords

[No Author keywords available]

Indexed keywords

3,4,5 TRIHYDROXYPIPERIDINE; PIPERIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032544527     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971535m     Document Type: Article
Times cited : (16)

References (28)
  • 3
    • 7344228184 scopus 로고    scopus 로고
    • U.S. Pat. US 5,017,563, 1991
    • (b) Liu, P. S.; Rhinehart, B. L.; Daniel, J. K. U.S. Pat. US 5,017,563, 1991; Chem. Abstr. 1991, 115, 136471e.
    • Liu, P.S.1    Rhinehart, B.L.2    Daniel, J.K.3
  • 4
    • 4243764258 scopus 로고
    • (b) Liu, P. S.; Rhinehart, B. L.; Daniel, J. K. U.S. Pat. US 5,017,563, 1991; Chem. Abstr. 1991, 115, 136471e.
    • (1991) Chem. Abstr. , vol.115
  • 15
    • 0030969628 scopus 로고    scopus 로고
    • Primary tosylates and mesylates have been used successfully to react with hydroxylamine in triethylamine at reflux, see: Goti, A.; Cicchi, S.; Fedi, V.; Nannelli, L.; Brandi, A. J. Org. Chem. 1997, 62, 3119.
    • (1997) J. Org. Chem. , vol.62 , pp. 3119
    • Goti, A.1    Cicchi, S.2    Fedi, V.3    Nannelli, L.4    Brandi, A.5
  • 22
    • 0026018819 scopus 로고
    • The coupling of alcohol and amine derivatives by the intramolecular Mitsunobu reactions has been reported. (a) Bernotas, R. C.; Cube, R. V. Tetrahedron Lett. 1991, 32, 161.
    • (1991) Tetrahedron Lett , vol.32 , pp. 161
    • Bernotas, R.C.1    Cube, R.V.2
  • 26
    • 0001774234 scopus 로고
    • Compounds 25 and 26 were prepared from the corresponding carbohydrates bearing the unprotected 6-hydroxyl group. The Mitsunobu reaction of those derivatives with N-hydroxyphthalimide followed by the treatment with hydrazine in methanol produced the desired hydroxylamine products 25 and 26. Grochowski, E.; Jurczak, J. Carbohydr. Res. 1976, 50, C15.
    • (1976) Carbohydr. Res. , vol.50
    • Grochowski, E.1    Jurczak, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.