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Volumn 53, Issue 5, 1997, Pages 1891-1908

Synthesis and stereochemistry of some heterocyclic saturated compounds based on l-p-nitrophenylserinol skeleton (II). 1-Aza-3,7-dioxabicyclo[3.3.0.]octanes

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[3.3.0]OCTANE DERIVATIVE; CHLORAMPHENICOL; HETEROCYCLIC COMPOUND; OXAZOLE DERIVATIVE; SCHIFF BASE;

EID: 0031550606     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)01105-2     Document Type: Article
Times cited : (23)

References (34)
  • 1
    • 0011322195 scopus 로고    scopus 로고
    • U. S.Pat. 2,777,854
    • 1. Edgerton, W., H.; Fisher, J., R., U. S.Pat. 2,777,854; Chem. Abstr. 1957, 51, P16541f-h
    • Edgerton, W.H.1    Fisher, J.R.2
  • 2
    • 4243559454 scopus 로고
    • 1. Edgerton, W., H.; Fisher, J., R., U. S.Pat. 2,777,854; Chem. Abstr. 1957, 51, P16541f-h
    • (1957) Chem. Abstr. , vol.51
  • 6
    • 4243769491 scopus 로고
    • 4. Nagawa, M., Takamine Kenkyujo Nempo, 1957, 9, 7-8; Chem. Abstr. 1958, 52, 307f
    • (1958) Chem. Abstr. , vol.52
  • 7
    • 0011377938 scopus 로고
    • 5. Nagawa, M., Yakugaku Zasshi, 1960, 80, 767-70; Chem. Abstr. 1960, 54, 24679b
    • (1960) Yakugaku Zasshi , vol.80 , pp. 767-770
    • Nagawa, M.1
  • 8
    • 85060508671 scopus 로고
    • 5. Nagawa, M., Yakugaku Zasshi, 1960, 80, 767-70; Chem. Abstr. 1960, 54, 24679b
    • (1960) Chem. Abstr. , vol.54
  • 12
    • 4243499541 scopus 로고
    • 8. Till, L.; Hischke, H.; Keilert, M.; Straetling, E., J., Ger.(East)DD 276,285 (C1.C07D498/04); Chem. Abstr. 1990, 113, P231361m
    • (1990) Chem. Abstr. , vol.113
  • 16
    • 0011284308 scopus 로고    scopus 로고
    • Preceeding paper (I)
    • 12. Preceeding paper (I)
  • 18
    • 0000312573 scopus 로고
    • 14 Compound 4b was previously mentioned (see Umezawa, S.; Suami, T., Bull. Chem. Soc. Japan, 1954, 27, 477-8 and Suami, T.; Uchide, J.; Umezawa, S., Bull. Chem. Soc. Japan, 1956, 29, 979) without any structural and pertinent description. CAUTION: the 1-naphthyl analogous of 4b was also identically prepared by us; it exhibits almost the same NMR features as 4b but the more overlapping observed make complete assignment uncertain.
    • (1954) Bull. Chem. Soc. Japan , vol.27 , pp. 477-478
    • Umezawa, S.1    Suami, T.2
  • 19
    • 0001666474 scopus 로고
    • without any structural and pertinent description. CAUTION: the 1-naphthyl analogous of 4b was also identically prepared by us; it exhibits almost the same NMR features as 4b but the more overlapping observed make complete assignment uncertain
    • 14 Compound 4b was previously mentioned (see Umezawa, S.; Suami, T., Bull. Chem. Soc. Japan, 1954, 27, 477-8 and Suami, T.; Uchide, J.; Umezawa, S., Bull. Chem. Soc. Japan, 1956, 29, 979) without any structural and pertinent description. CAUTION: the 1-naphthyl analogous of 4b was also identically prepared by us; it exhibits almost the same NMR features as 4b but the more overlapping observed make complete assignment uncertain.
    • (1956) Bull. Chem. Soc. Japan , vol.29 , pp. 979
    • Suami, T.1    Uchide, J.2    Umezawa, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.