Lithiation and reactions of stilbene oxides: synthetic utility.

Lithiation and reactions of stilbene oxides: synthetic utility.
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二苯乙烯氧化物的锂化和反应:合成用途。

DOI:
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发表时间:
2004
期刊:
影响因子:
5.2
通讯作者:
A. Salomone
A. Salomone
中科院分区:
化学1区
文献类型:
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作者:
S. Florio;V. Aggarwal;A. Salomone

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被引文献

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研究了反式和顺式二苯乙烯氧化物(+/-)-1和8的锂化反应。而对于8,锂化仅发生在苄基位置,对于反式异构体(+/-)-1,邻位锂化与α-锂化竞争,这取决于实验条件。证明了α-锂化的顺式-和反式-二苯乙烯氧化物(+/-)-2和(+/-)-9的构型稳定性,以及标位二苯乙烯氧化物(R,R)-2的构型稳定性。
The lithiation of trans- and cis-stilbene oxides (+/-)-1 and 8 has been investigated. While with 8, lithiation occurred exclusively at the benzylic position, with the trans isomer (+/-)-1, ortho-lithiation competed with alpha-lithiation depending upon the experimental conditions. The configurational stability of the alpha-lithiated cis- and trans-stilbene oxides (+/-)-2 and (+/-)-9, respectively, was proved as well as that of scalemic stilbene oxide (R,R)-2.