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Volumn 36, Issue 8, 1995, Pages 1197-1200

An unequivocal synthesis of the ring-A,B dihydropyrromethenone of phytochrome

Author keywords

[No Author keywords available]

Indexed keywords

DIHYDROPYRROMETHENONE; PHYTOCHROME; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0028860086     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)00032-8     Document Type: Article
Times cited : (20)

References (39)
  • 11
    • 0002551784 scopus 로고
    • For a review of linear tetrapyrrole chemistry see:
    • (1983) Tetrahedron , vol.39 , pp. 1839
  • 12
    • 84914022591 scopus 로고    scopus 로고
    • Symposia-In-Print, Bonnett, R., Ed.(j)
  • 18
    • 84982064214 scopus 로고
    • Synthesen von Gallenfarbstoffen, X. Synthese und Photoisomerisierung desracem. Phytochromobilin-dimethylesters
    • (1980) Chemische Berichte , vol.113 , pp. 1603
    • Gossauer1    Weller2
  • 29
    • 84914022590 scopus 로고    scopus 로고
    • 10 does not appear to be a general reaction, but this reagent works well with carboxylic acids where intramolecular participation is possible. The scope of this reaction is currently under investigation.
  • 38
    • 84914022588 scopus 로고    scopus 로고
    • 3): δ 1.25 (d, J = 7.20 Hz, 3H), 1.37 (d, J = 7.50 Hz, 3H), 1.82 (s, 3H), 2.09 (s, 3H), 2.52 (m, 1H), 2.58 (t, J = 8.10 Hz, 2H), 3.02 (t, J = 8.10 Hz, 2H), 3.61 (m, 1H), 3.67 (s, 3H), 3.79 (s, 3H), 4.49 (d, J = 15.00 Hz, 1H), 4.89 (d, J = 15.00 Hz, 1H), 5.55 (s, 1H), 6.85 (d, J = 8.70 Hz, 2H), 7.22 (d, J = 8.70 Hz, 2H), 9.13 (br, 1H), 9.56 (s, 1H). Copies of NMR spectra will be provided upon request.
  • 39
    • 84914022587 scopus 로고    scopus 로고
    • Financial support of this work by NIH, Grant No. GM38913, is gratefully acknowledged.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.