Synthesis of BCP Benzylamines From 2-Azaallyl Anions and [1.1.1]Propellane

Exploring the Steric and Electronic Factors Governing the Regio- and Enantioselectivity of the Pd-Catalyzed Decarboxylative Generation and Allylation of 2-Azaallyl Anions

(2018) Shuaifei Wang et al.   JOURNAL OF ORGANIC CHEMISTRY

2-Azaallyl Anions, 2-Azaallyl Cations, 2-Azaallyl Radicals, and Azomethine Ylides

(2018) Shaojian Tang et al.   CHEMICAL REVIEWS

Transition-Metal-Free Radical C(sp3)–C(sp2) and C(sp3)–C(sp3) Coupling Enabled by 2-Azaallyls as Super-Electron-Donors and Coupling-Partners

(2017) Minyan Li et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Radical Multicomponent Carboamination of [1.1.1]Propellane

(2017) Junichiro Kanazawa et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Transition-metal-free chemo- and regioselective vinylation of azaallyls

(2017) Minyan Li et al.   Nature Chemistry

Toward Resolving the Resveratrol Conundrum: Synthesis and in Vivo Pharmacokinetic Evaluation of BCP–Resveratrol

(2017) Yi Ling Goh et al.   ACS Medicinal Chemistry Letters

Strain-release amination

(2016) R. Gianatassio et al.   SCIENCE

Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA2 Inhibitor

(2016) Nicholas D. Measom et al.   ACS Medicinal Chemistry Letters

Evaluation oftert-Butyl Isosteres: Case Studies of Physicochemical and Pharmacokinetic Properties, Efficacies, and Activities

(2015) Matthias V. Westphal et al.   ChemMedChem

Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor

(2012) Antonia F. Stepan et al.   JOURNAL OF MEDICINAL CHEMISTRY