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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF FLUORINE ANALOGS OF PROTOPORPHYRIN POTENTLALLY USEFUL FOR DIAGNOSIS AND THERAPY OF CANCER PART 3.~1 SYNTHESIS OF (2,2-DIFLUOROVINYL)-TRIFLUOROVINYL- AND (1-CHLORO-2,2-DIFLUOROVINYL)-(2,2-DIFLUOROVINYL)DEUTEROPORPHYRIN
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SYNTHESIS OF FLUORINE ANALOGS OF PROTOPORPHYRIN POTENTLALLY USEFUL FOR DIAGNOSIS AND THERAPY OF CANCER PART 3.~1 SYNTHESIS OF (2,2-DIFLUOROVINYL)-TRIFLUOROVINYL- AND (1-CHLORO-2,2-DIFLUOROVINYL)-(2,2-DIFLUOROVINYL)DEUTEROPORPHYRIN

机译:可用于诊断和治疗癌症的原卟啉类似物的氟类似物的合成3.〜1合成(2,2-二氟乙烯基)-三氟乙烯基-和(1-氯-2,2-二氟乙烯基)-(2,2-二氟)氘卟啉

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摘要

Wittig reaction of 3-and 8-formyl deuteroporphyrin dimethyl esters (1 or 2) with triphenylphosphonium difluoromethylide,generated in situ from sodium chlordifluoroacetate an triphenylphosphine,gave 3-and 8-difluorovinyl cmpounds (3 or 4),which were iodinated to form corresponding 8-and 3-iodo compounds (5 or 6). Coupling reaction of these iodo compounds with our new bis(fluorovinyl)zinc reagents afforded the titled compounds (7 to 10)in moderate to good yields.
机译:由氯二氟乙酸钠原位生成的三苯基三氟膦酸三和3-甲氧基氘卟啉二甲酯(1或2)与三苯基膦的Wittig反应,制得3-和8-二氟乙烯基cmpounds(3或4),将其碘化成相应的8和3碘化合物(5或6)。这些碘代化合物与我们的新型双(氟乙烯基)锌试剂的偶联反应以中等至良好的产率提供了标题化合物(7至10)。

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