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Volumn 39, Issue 14, 1998, Pages 2001-2004

Heterolignanolides. Synthesis of a new family of Thienolignanolides

Author keywords

[No Author keywords available]

Indexed keywords

ETOPOSIDE; FURANONE DERIVATIVE; HETEROCYCLIC COMPOUND; LIGNAN DERIVATIVE; PODOPHYLLIN; PODOPHYLLOTOXIN; PODOPHYLLOTOXIN DERIVATIVE; TENIPOSIDE; TETRALIN DERIVATIVE;

EID: 0032473901     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00116-6     Document Type: Article
Times cited : (12)

References (38)
  • 8
    • 0010586403 scopus 로고    scopus 로고
    • Non systematic numbering is adopted for heterolignans to maintain the accepted numbering for lignans (see ref. 1a and references therein). In this situation, it is assumed that the heteroatom X replaces positions 2 and 3
    • 3. Non systematic numbering is adopted for heterolignans to maintain the accepted numbering for lignans (see ref. 1a and references therein). In this situation, it is assumed that the heteroatom X replaces positions 2 and 3.
  • 29
    • 33645171714 scopus 로고
    • 4 treatment. No aromatization products were observed for thiophene derivatives in any case
    • 4 treatment. No aromatization products were observed for thiophene derivatives in any case.
    • (1988) Tetrahedron Lett. , vol.29 , pp. 2429
    • Jung, M.E.1    Gervay, J.2
  • 31
    • 0010623105 scopus 로고    scopus 로고
    • See also 8 and references therein
    • b) See also 8 and references therein.
  • 32
    • 0010550187 scopus 로고    scopus 로고
    • 1H-NMR spectrum of 5 shows C-7′ and C-8′ as two broad singlets, in agreement with a trans relationship between this pair of protons and a cis relationship between C-8 and C-8′
    • 1H-NMR spectrum of 5 shows C-7′ and C-8′ as two broad singlets, in agreement with a trans relationship between this pair of protons and a cis relationship between C-8 and C-8′.
  • 35
    • 0010620705 scopus 로고    scopus 로고
    • ref. 6a
    • c) ref. 6a.
  • 36
    • 0010552861 scopus 로고    scopus 로고
    • note
    • 3, 20C MHz) δ 7.27 (d, J = 5.1, 1H); 6.67 (d, J = 5.1, 1H); 6.37 (s, 2H); 4.97 (d, J = 7.7, 1H); 4.60 (d J = 4.0, 1H); 4.50 (dd, J = 6.6, 8.4, 1H); 4.01 (dd, J = 6.8, 8.7, 1H); 3.02-2.86 (m, 2H); 0.94 (s, 9H); 0.27 (s, 3H); 0.11 (s, 3H)
  • 38
    • 0010585624 scopus 로고    scopus 로고
    • note
    • 3 in 2,3-disubstituted thiophene are 125.68° and 123.28° respectively, higher than those for benzene (120° each), further increasing the strain of the 7',8-cis-8,8'-trans cyclolignanolides.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.