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594306435

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用亚磷酸三乙酯代替三苯基膦所制得的磷Ylide与醛酮反应称为Wittig-Horner反应。该反应有两个优点：一是它容易和醛酮反应，有些有三苯基膦制备的磷叶立德，特别是当α碳上带有羰基时，比较稳定，不容易和酮带有，有时需加入苯甲酸作为催化剂。二是反应中的另一产物，O,O-二乙基磷酸钠溶于水，无需像三苯基膦的叶立德时，还需要分离三苯氧膦。三是磷酸酯的反应，立体选择性很强，产物主要是反式。

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1楼 2011-04-11 10:58:41

已阅回复此楼关注TA 给TA发消息送TA红花 TA的回帖

slz146

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594306435(金币+15, 翻译EPI+1): 谢谢 2011-04-16 18:58:17

Triethyl phosphate which was instead of Triphenylphosphine was prepared for P-ylide . Wittig-Horner reaction was Defined as the reaction of Keto-Aldehyde and above P-ylide . This reaction had two advantages: The first was that it could react with Keto-Aldehyde easily , some P-ylide which was prepared by Triphenylphosphine , especially as there was carbonyl on α-Cedrene , it was Relatively stable and it could not be with ketone easily , sometimes it might be needed benzoic acid as catalyst . The second was that Another product of the reaction: O, O - diethyl sodium was soluble in water , Triphenylphosphine oxide did not need to be separated when P-ylide was prepared by Triphenylphosphine . The third was that the reaction of phosphoric ester had very strong stereoselectivity , and the product of the reaction was mainly antiform .

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