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首页> 外文期刊>Tetrahedron >REGIOSELECTIVE SYNTHESIS OF SUBSTITUTED PTEROCARPANS AND PTEROCARPENES - LEWIS ACID TI(IV) PROMOTED FORMAL (3+2) CYCLOADDITION REACTIONS
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REGIOSELECTIVE SYNTHESIS OF SUBSTITUTED PTEROCARPANS AND PTEROCARPENES - LEWIS ACID TI(IV) PROMOTED FORMAL (3+2) CYCLOADDITION REACTIONS

机译:取代的五聚体和四碳的区域选择性合成-路易斯酸TI(IV)促进了正式的(3 + 2)循环负载反应

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摘要

A synthesis of novel pterocarpans (8a-e, 10a-e and 11a-e) and pterocarpenes (7a-d and 9a-c) has been carried out. This method involves the Lewis acid Ti (TV) promoted formal (3+2) cycloaddition reaction of 2-alkoxy-1,4-benzoquinones (6a-c) with appropriately substituted 2H-chromenes (1a-b, 2a-b and 5) at -78 degrees C. [References: 22]
机译:已经合成了新的角果皮(8a-e,10a-e和11a-e)和角皮烯(7a-d和9a-c)。该方法涉及路易斯酸Ti(TV)促进2-烷氧基-1,4-苯醌(6a-c)与适当取代的2H-色烯(1a-b,2a-b和5 )在-78摄氏度。[参考:22]

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