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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF CHAETOMELLIC ANHYDRIDE A,A POTENT INHIBITOR OF RAS PROTEIN FARNESYL TRANSFERASE
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SYNTHESIS OF CHAETOMELLIC ANHYDRIDE A,A POTENT INHIBITOR OF RAS PROTEIN FARNESYL TRANSFERASE

机译:RAS蛋白法呢基转移酶的强效抑制剂-脂肪族酸酐A的合成

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摘要

Chaetomellic anhydride A,a potent inhibitor of Ras protein farnesyltransferase,was synthesized in 61% yield over four steps from methyl propionate.The synthesis features palladium-catalyzed carboxylation reaction under Cacchi conditions,efficiently incorporating carbon monoxide generated in situ from acetic formic anhydride into beta-carbomethoxyalkenyl triflate,and giving rise to the maleic anhydride motif of chaetomellic anhydride A.Noteworthy is the remarkable reactivity of the carboxylation reaction that takes place at room temperature despite the fact that common palladium-catalyzed carboxylations generally require rather harsh conditions.The scope of the method is also presented.
机译:Chaetomellic酐A是一种有效的Ras蛋白法呢基转移酶抑制剂,由丙酸甲酯经四个步骤合成,收率为61%。该合成的特征是在Cacchi条件下钯催化的羧化反应,有效地将乙酸酐中的一氧化碳有效地引入β中。 -甲氧基羰基烯基三氟甲磺酸酯,并产生Chaetomellic酸酐A的马来酸酐基序。值得注意的是,尽管通常的钯催化的羧化反应通常需要相当苛刻的条件,但室温下的羧化反应仍具有显着的反应性。还介绍了该方法。

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