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Volumn 64, Issue 37, 2008, Pages 8709-8715

Synthesis of new amphiphilic chlorin derivatives from protoporphyrin-IX dimethyl ester

Author keywords

[No Author keywords available]

Indexed keywords

2 1 [(2 HYDROXYETHYL)CARBAMOYL] 13,17 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,12,18 TETRAMETHYL 8 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 [(2 HYDROXYETHYL)CARBAMOYL] 8,12 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,13,17 TETRAMETHYL 18 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 [[2 [2 (2 HYDROXYETHOXY)ETHOXY]ETHOXY]CARBONYL] 13,17 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,12,18 TETRAMETHYL 8 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 [[2 [2 (2 HYDROXYETHOXY)ETHOXY]ETHOXY]CARBONYL] 8,12 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,13,17 TETRAMETHYL 18 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 [[2 [2 (2 METHOXYETHOXY)ETHOXY]ETHOXY]CARBONYL] 13,17 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,12,18 TETRAMETHYL 8 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 [[2 [2 (2 METHOXYETHOXY)ETHOXY]ETHOXY]CARBONYL] 8,12 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,13,17 TETRAMETHYL 18 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 METHOXYCARBONYL 13,17 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,12,18 TETRAMETHYL 8 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; 2 1 METHOXYCARBONYL 8,12 BIS[2 (METHOXYCARBONYL)ETHYL] 2,7,13,17 TETRAMETHYL 18 VINYL 2,2 1,2 2,2 3 TETRAHYDROBENZO[B]PORPHYRIN 2 2 CARBOXYLIC ACID; MALEIC ANHYDRIDE; PROTOPORPHYRIN; PROTOPORPHYRIN DIMETHYL ESTER;

EID: 48049100962     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.06.103     Document Type: Article
Times cited : (32)

References (38)
  • 25
    • 84945050150 scopus 로고
    • To simplify the discussion of the reactivity and the NMR spectra, carbon atoms in structures 5-8 were numbered as in protoporphyrin-IX. However, for the systematic names the IUPAC recommendations are being used for fused porphyrins:
    • To simplify the discussion of the reactivity and the NMR spectra, carbon atoms in structures 5-8 were numbered as in protoporphyrin-IX. However, for the systematic names the IUPAC recommendations are being used for fused porphyrins:. Moss G.P. Pure Appl. Chem. 59 (1987) 779
    • (1987) Pure Appl. Chem. , vol.59 , pp. 779
    • Moss, G.P.1
  • 26
    • 48049125030 scopus 로고    scopus 로고
    • {A figure is presented}
    • {A figure is presented}


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.