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Volumn 54, Issue 25, 1998, Pages 6987-6998

Synthesis of oxazines and thiazines by cyclodehydration of hydroxy amides and thioamides

Author keywords

[No Author keywords available]

Indexed keywords

OXAZINE DERIVATIVE; THIAZINE DERIVATIVE;

EID: 0032543530     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(98)00341-X     Document Type: Article
Times cited : (68)

References (63)
  • 2
    • 84943425073 scopus 로고
    • A. R. Katritzky and C. W. Rees, Eds.; Pergamon Press: Oxford
    • (b) Sainsbury, M. In Comprehensive Heterocyclic Chemistry, A. R. Katritzky and C. W. Rees, Eds.; Pergamon Press: Oxford, 1984; Vol. 3; pp 995.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 995
    • Sainsbury, M.1
  • 21
    • 0030199693 scopus 로고    scopus 로고
    • Burgess reagent = methyl(carboxysulfamoyl)triethylammonium hydroxide, inner salt
    • (b) Wipf, P.; Venkatraman, S. Tetrahedron Lett. 1996, 37, 4659. Burgess reagent = methyl(carboxysulfamoyl)triethylammonium hydroxide, inner salt.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4659
    • Wipf, P.1    Venkatraman, S.2
  • 26
    • 0027054354 scopus 로고
    • 20. For some applications in total synthesis, see: (a) Wipf, P.; Miller, C. P. J. Am. Chem. Soc. 1992, 114, 10975.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10975
    • Wipf, P.1    Miller, C.P.2
  • 49
    • 0010420933 scopus 로고
    • (b) Elliott, D. F. J. Chem. Soc. 1949, 589; ibid. 1950, 62.
    • (1950) J. Chem. Soc. , pp. 62
  • 53
    • 0010421072 scopus 로고    scopus 로고
    • note
    • 25. For a discussion of steric and electronic effects in the thiolysis of oxazolines, see ref. 16a.
  • 55
    • 0010500797 scopus 로고    scopus 로고
    • note
    • 27. For a discussion of the effects of leaving groups and substrate stereochemistry as well as reaction conditions on the formation of five-membered oxazolines vs three-membered aziridines in β-hydroxy-α-amino acid cyclodehydrations, see ref. 21h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.