6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755, United States.
Org Lett. 2012 Aug 17;14(16):4238-41. doi: 10.1021/ol301935q. Epub 2012 Aug 7.
Although the pyramidal inversion barriers in diphosphines (R(2)P-PR(2)) are similar to those in phosphines (PR(3)), P-stereogenic chiral diphosphines have rarely been exploited as building blocks in asymmetric synthesis. The synthesis, reactivity, and resolution of the benzodiphosphetane trans-1,2-(P(t-Bu))(2)C(6)H(4) are reported. Alkylation with MeOTf followed by addition of a nucleophile gave the useful C(2)-symmetric P-stereogenic ligand BenzP* and novel analogues.
尽管二膦(R(2)P-PR(2))中的三角锥形反转势垒与膦(PR(3))中的相似,但手性 P-二膦作为构建块在不对称合成中很少被利用。本文报道了苯并二磷杂环戊烷反式-1,2-(P(t-Bu))(2)C(6)H(4)的合成、反应性和拆分。用 MeOTf 进行烷基化,然后加入亲核试剂,得到了有用的 C(2)对称 P-手性配体 BenzP*和新型类似物。