Nguyen Terrence-Thang H, Navarro Antonio, Ruble J Craig, Davies Huw M L
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, United States.
Org Lett. 2024 Apr 12;26(14):2832-2836. doi: 10.1021/acs.orglett.3c03652. Epub 2024 Jan 3.
Although cyclopropanation with donor/acceptor carbenes can be conducted under low catalyst loadings (<0.001 mol %), such low loading has not been generally effective for other classes of carbenes such as acceptor carbenes. In this current study, we demonstrate that ethyl diazoacetate can be effectively used in the cyclopropanation of -Boc-2,5-dihydropyrrole with dirhodium(II) catalyst loadings of 0.005 mol %. By appropriate choice of catalyst and hydrolysis conditions, either the - or -3-azabicyclo[3.1.0]hexanes can be formed cleanly with high levels of diastereoselectivity with no chromatographic purification.
尽管供体/受体卡宾的环丙烷化反应可以在低催化剂负载量(<0.001 mol%)下进行,但如此低的负载量对其他类型的卡宾(如受体卡宾)通常无效。在本研究中,我们证明重氮乙酸乙酯可以有效地用于在0.005 mol%的二铑(II)催化剂负载量下与 -Boc-2,5-二氢吡咯进行环丙烷化反应。通过适当选择催化剂和水解条件,可以以高非对映选择性清晰地形成 - 或 -3-氮杂双环[3.1.0]己烷,无需色谱纯化。