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Volumn 34, Issue 18, 1993, Pages 2883-2886

A rational step-by-step preparation of a chlorin from linear tetrapyrroles

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIN DERIVATIVE; PORPHYRIN DERIVATIVE; PYRROLE DERIVATIVE; TETRAPYRROLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0027156784     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)60471-9     Document Type: Article
Times cited : (17)

References (24)
  • 6
    • 3142580582 scopus 로고
    • For a more thorough treatment of the chlorin synthesis in the preparation of chlorophyll a, see
    • (1990) Tetrahedron , vol.46 , pp. 7599-7659
    • Woodward1
  • 10
    • 33947658957 scopus 로고
    • Synthetic studies relevant to biosynthetic research on vitamin B12. Part 1. Syntheses of C-methylated chlorins based on 1-pyrrolines (3,4-dihydropyrroles)
    • A few preparations of chlorins with specific substitution pattern, e.g., those with a gem dimethyl β-substituted reduced ring, have utilized a non-oxidizable 3,4-dihydropyrrole in a synthesis where the macrocycles are formed in a step-by-step manner. See
    • (1984) Journal of the Chemical Society, Perkin Transactions 1 , pp. 2725-2732
    • Battersby1    Fookes2    Snow3
  • 13
    • 0001835870 scopus 로고
    • Metallkomplexe mit tetrapyrrol-liganden, V Zum einfluß des zentralmetalls auf die hydrierung des octaäthylporphin-systems
    • (1972) Tetrahedron Letters , vol.36 , pp. 3803-3806
    • Buchler1    Schneehage2
  • 15
    • 84918709609 scopus 로고    scopus 로고
    • All solvents were degassed either by bubbling argon overnight or by the freeze-thaw method. All MacDonald condensations and manipulations of phlorin and porphodimethenes were run under anaerobic conditions in Schlenk-ware.
  • 18
    • 84918765389 scopus 로고    scopus 로고
    • 3), 3.10, t, 2H, J=8.01 [[Truncated]]
  • 19
    • 84918724033 scopus 로고    scopus 로고
    • SYBYL and Alchemy 3 force field calculations were used.
  • 20
    • 37049088717 scopus 로고
    • Syntheses of chlorins from unsymmetrically substituted iron porphyrins
    • Sodium reduction of hemes show a preference for the reduction of β-hydrogen substituted rings over those rings that contain electron-releasing alkyl substituents.
    • (1988) Journal of the Chemical Society, Perkin Transactions 1 , pp. 3119-3131
    • Burns1    Lai2    Smith3
  • 22
    • 84918709286 scopus 로고    scopus 로고
    • 3 and warming to 55° C for one hour yielded 5b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.