University of Florida , Department of Chemistry, P.O. Box 117200, Gainesville, Florida 32611, United States.
Org Lett. 2017 Aug 4;19(15):4130-4133. doi: 10.1021/acs.orglett.7b01951. Epub 2017 Jul 19.
Cope and co-workers reported the [3,3] rearrangement of 3,3-dicyano-1,5-dienes in the early 1940s ("The Cope rearrangement"). However, these original substrates have remained largely unstudied until recently. Herein we explore styrene-deconjugating Cope rearrangements, a diastereoselective Cope rearrangement/deconjugative α-allylation sequence, and factors governing α- vs γ-allylation regioselectivity of Knoevenagel adduct allyl anions. Ultimately, these studies result in the synthesis of diverse and functionally dense polycycloalkane frameworks from abundant reagents using simple chemistry.
科普及其同事在 20 世纪 40 年代早期报道了[3,3]重排 3,3-二氰基-1,5-二烯(“科普重排”)。然而,直到最近,这些原始底物才得到广泛研究。在此,我们探讨了去共轭 Cope 重排、非对映选择性 Cope 重排/去共轭α-烯丙基化序列以及影响 Knoevenagel 加成物烯丙基阴离子α-与γ-烯丙基化区域选择性的因素。最终,这些研究利用简单的化学方法从丰富的试剂中合成了具有多种功能的稠环烷烃骨架。