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Volumn 19, Issue 1, 2011, Pages 52-57

Reduction of vinyl groups in naturally occurring chlorophylls-a

Author keywords

Biosynthesis; Hydrogenation; Regioisomer; Site selectivity; Substitution effect

Indexed keywords

ACETONE; ALUMINUM; CHLORINE; CHLOROPHYLL A; PORPHYRIN; RHODIUM; VINYL DERIVATIVE;

EID: 78650720803     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2010.11.056     Document Type: Article
Times cited : (13)

References (20)
  • 8
    • 84871806219 scopus 로고    scopus 로고
    • V.L. Kolossov, and C.A. Rebeiz C.A. Rebeiz, C. Benning, H.J. Bohnert, H. Daniell, J.K. Hoober, H.K. Lichtenthaler, A.R. Portis, B.C. Tripathy, The Chloroplast: Basic and Applications 2010 Springer Dordrecht, The Netherlands 25 38 Chapter 2
    • (2010) The Chloroplast: Basic and Applications , pp. 25-38
    • Kolossov, V.L.1    Rebeiz, C.A.2
  • 17
    • 78650724671 scopus 로고    scopus 로고
    • note
    • 2 with the C7C8. Therefore, the 3-vinyl group is more isolated from the adjacent π-system than the 8-vinyl group, and the former is a more reactive vinyl moiety than the latter. A porphyrin π-conjugated skeleton is more symmetric than the chlorin and two different 18π-conjugated systems are possible in the porphyrin. One of π-systems includes the C7C8 double bond. Both the 3- and 8-vinyl groups of 6 are connected with such largely delocalized 18π-systems, giving the same reactivity for the present hydrogenation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.