首页> 外文期刊>Chemistry: A European journal >1,4-pentenyne as a five-carbon synthon for efficient and selective syntheses of natural products containing 2,4-dimethyl-1-penten-1,5-ylidene and related moieties by means of Zr-catalyzed carboalumination of alkynes and alkenes
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1,4-pentenyne as a five-carbon synthon for efficient and selective syntheses of natural products containing 2,4-dimethyl-1-penten-1,5-ylidene and related moieties by means of Zr-catalyzed carboalumination of alkynes and alkenes

机译:1,4-戊烯作为五碳合成子,用于通过Zr催化炔烃和烯烃的碳铝催化有效和选择性地合成包含2,4-二甲基-1-戊烯-1,5-亚烷基和相关部分的天然产物

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摘要

Two highly efficient protocols for enantioselective synthesis of 2,4-dimethyl-1-penten-1,5-ylidene derivatives involve the combined use of the Zr-catalyzed methylalumination of alkynes (ZMA) and the Zr-catalyzed asymmetric carboalumination of alkenes (ZACA). The ZMA/ZACA protocol has been applied to the synthesis of a nafuredin intermediate 14 and a potential intermediate 18 for milbemycin beta(3), while the ZACA/ZMA protocol has been applied to the synthesis of a (-)-bafilomycin A(1) intermediate 25.
机译:对映选择性合成2,4-二甲基-1-戊烯-1,5-亚烷基衍生物的两个高效方案涉及Zr催化的炔烃甲基铝化(ZMA)和Zr催化的烯烃不对称碳铝化(ZACA)的组合使用)。 ZMA / ZACA协议已被用于合成米尔布霉素beta(3)的那富瑞丁中间体14和潜在的中间体18,而ZACA / ZMA协议已被应用于合成(-)-bafilomycin A(1) )中级25。

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