Related references
Note: Only part of the references are listed.Visible-Light-Induced 1,3-Aminopyridylation of [1.1.1]Propellane with N-Aminopyridinium Salts
Sanghoon Shin et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2021)
Synthesis of an elusive, stable 2-azaallyl radical guided by electrochemical and reactivity studies of 2-azaallyl anions
Grace B. Panetti et al.
CHEMICAL SCIENCE (2021)
Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives
Masaki Kondo et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
1,3-Difunctionalizations of [1.1.1]Propellane via 1,2-Metallate Rearrangements of Boronate Complexes
Songjie Yu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
Divergent Strain-Release Amino-Functionalization of [1.1.1]Propellane with Electrophilic Nitrogen-Radicals
Ji Hye Kim et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
Copper-mediated synthesis of drug-like bicyclopentanes
Xiaheng Zhang et al.
NATURE (2020)
Continuous Flow-Enabled Synthesis of Bench-Stable Bicyclo[1.1.1]pentane Trifluoroborate Salts and Their Utilization in Metallaphotoredox Cross-Couplings
Michael D. VanHeyst et al.
ORGANIC LETTERS (2020)
A General C(sp3)-C(sp3) Cross-Coupling of Benzyl Sulfonylhydrazones with Alkyl Boronic Acids
Rohan R. Merchant et al.
ORGANIC LETTERS (2020)
Recent advances in the applications of [1.1.1]propellane in organic synthesis
Fu-Sheng He et al.
CHINESE CHEMICAL LETTERS (2020)
Diverse functionalization of strong alkyl C-H bonds by undirected borylation
Raphael Oeschger et al.
SCIENCE (2020)
Expanding the Medicinal Chemist Toolbox: Comparing Seven C(sp2)-C(sp3) Cross-Coupling Methods by Library Synthesis
Amanda W. Dombrowski et al.
ACS MEDICINAL CHEMISTRY LETTERS (2020)
Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate
Yukiya Sato et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to [1.1.1]Propellane
Kuno Schwaerzer et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)
Aminoalkylation of [1.1.1]Propellane Enables Direct Access to High-Value 3-Alkylbicyclo[1.1.1]pentan-1-amines
Jonathan M. E. Hughes et al.
ORGANIC LETTERS (2019)
A General Route to Bicyclo[1.1.1]pentanes through Photoredox Catalysis
Jeremy Nugent et al.
ACS CATALYSIS (2019)
Zn-Mediated Fragmentation of Tertiary Alkyl Oxalates Enabling Formation of Alkylated and Arylated Quaternary Carbon Centers
Yang Ye et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)
Organocopper cross-coupling reaction for C-C bond formation on highly sterically hindered structures
Miku Oi et al.
CHEMICAL SCIENCE (2019)
Saturated bioisosteres of benzene: where to go next?
Pavel K. Mykhailiuk
ORGANIC & BIOMOLECULAR CHEMISTRY (2019)
A Modular Approach to the Synthesis of gem-Disubstituted Cyclopropanes
Michael R. Harris et al.
ORGANIC LETTERS (2018)
Synthesis and applications of highly functionalized 1-halo-3-substituted bicyclo[1.1.1]pentanes
Dimitri F. J. Caputo et al.
CHEMICAL SCIENCE (2018)
Synthesis of BCP Benzylamines From 2-Azaallyl Anions and [1.1.1]Propellane
Russell A. Shelp et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2018)
2-Azaallyl Anions, 2-Azaallyl Cations, 2-Azaallyl Radicals, and Azomethine Ylides
Shaojian Tang et al.
CHEMICAL REVIEWS (2018)
Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer
David N. Primer et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)
Radical Multicomponent Carboamination of [1.1.1]Propellane
Junichiro Kanazawa et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)
Construction of 1-Heteroary1-3-azabicyclo[3.1.0]hexanes by sp3-sp2 Suzuki-Miyaura and Chan-Evans-Lam Coupling Reactions of Tertiary Trifluoroborates
Michael R. Harris et al.
ORGANIC LETTERS (2017)
Photoinduced decarboxylative borylation of carboxylic acids
Alexander Fawcett et al.
SCIENCE (2017)
Recent Developments in Organoboron Chemistry: Old Dogs, New Tricks
James W. B. Fyfe et al.
CHEM (2017)
Synthesis of Bicyclo[1.1.1]pentane Bioisosteres of Internal Alkynes and para-Disubstituted Benzenes from [1.1.1]Propellane
Ilya S. Makarov et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Stereospecific functionalizations and transformations of secondary and tertiary boronic esters
Christopher Sandford et al.
CHEMICAL COMMUNICATIONS (2017)
Propellanes-From a Chemical Curiosity to Explosive Materials and Natural Products
Alicia M. Dilmac et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Redox-Active Esters in Fe-Catalyzed C-C Coupling
Fumihiko Toriyama et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)
Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures
Cathleen M. Crudden et al.
NATURE COMMUNICATIONS (2016)
Nickel-Catalyzed Reductive Coupling of Aryl Bromides with Tertiary Alkyl Halides
Xuan Wang et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2015)
Enantiospecific sp2-sp3 coupling of secondary and tertiary boronic esters
Amadeu Bonet et al.
NATURE CHEMISTRY (2014)
Synthesis of diarylmethylamines via palladium-catalyzed regioselective arylation of 1,1,3-triaryl-2-azaallyl anions
Minyan Li et al.
CHEMICAL SCIENCE (2014)
Ate Complexes of Secondary Boronic Esters as Chiral Organometallic-Type Nucleophiles for Asymmetric Synthesis
Robin Larouche-Gauthier et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success
Frank Lovering et al.
JOURNAL OF MEDICINAL CHEMISTRY (2009)
Share Paper
