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;
ADDITION REACTION;
ARTICLE;
CYCLOADDITION;
DIELS ALDER REACTION;
DRUG SYNTHESIS;
PHOTOCHEMISTRY;
PHYSICAL CHEMISTRY;
PRIORITY JOURNAL;
ALNUS;
3
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25
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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
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{A figure is presented}
{A figure is presented}
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