New strategies for the synthesis of aliphatic azides
P Sivaguru, Y Ning, X Bi - Chemical Reviews, 2021 - ACS Publications
Aliphatic azides are a versatile class of compounds found in a variety of biologically active
pharmaceuticals. These compounds are also recognized as useful precursors for the …
pharmaceuticals. These compounds are also recognized as useful precursors for the …
Chemical versatility of azide radical: journey from a transient species to synthetic accessibility in organic transformations
M Shee, NDP Singh - Chemical Society Reviews, 2022 - pubs.rsc.org
The generation of azide radical (N3˙) occurs from its precursors primarily via a single
electron transfer (SET) process or homolytic cleavage by chemical methods or advanced …
electron transfer (SET) process or homolytic cleavage by chemical methods or advanced …
[HTML][HTML] Radical azidation as a means of constructing C (sp3)-N3 bonds
L Ge, MF Chiou, Y Li, H Bao - Green Synthesis and Catalysis, 2020 - Elsevier
The azido group is found in large numbers of natural products, drugs, biochemicals and
materials and to date, many elegant and useful methods for the synthesis of organic azides …
materials and to date, many elegant and useful methods for the synthesis of organic azides …
Direct synthesis of unprotected 2-azidoamines from alkenes via an iron-catalyzed difunctionalization reaction
S Makai, E Falk, B Morandi - Journal of the American Chemical …, 2020 - ACS Publications
Unprotected, primary 2-azidoamines are versatile precursors to vicinal diamines, which are
among the most common motifs in biologically active compounds. Herein, we report their …
among the most common motifs in biologically active compounds. Herein, we report their …
Tandem Electrochemical Oxidative Azidation/Heterocyclization of Tryptophan‐Containing Peptides under Buffer Conditions
Y Weng, X Xu, H Chen, Y Zhang… - Angewandte Chemie, 2022 - Wiley Online Library
As the aromatic tryptophan (Trp) side chain plays a pivotal role in influencing the structure
and function of peptides and proteins, it has become an attractive target for the late‐stage …
and function of peptides and proteins, it has become an attractive target for the late‐stage …
Photo-induced stereo-and regiospecific sulfonylation of C–C multiple bonds exploiting the dual reactivity of sulfonium iodate (i) species
Vinyl sulfones are privileged motifs for assembling prevalent biologically active molecules
and represent “gateway functional groups” in medicinal chemistry and drug discovery …
and represent “gateway functional groups” in medicinal chemistry and drug discovery …
Photoinduced Rapid Multicomponent Cascade Reaction of Aryldiazonium Salts with Unactivated Alkenes and TMSN3
J Shen, J Xu, L He, Y Ouyang, L Huang, W Li… - Organic …, 2021 - ACS Publications
The first example of a photoinduced rapid multicomponent cascade reaction of
aryldiazonium salts with unactivated alkenes and trimethylsilyl azide (TMSN3) under oxidant …
aryldiazonium salts with unactivated alkenes and trimethylsilyl azide (TMSN3) under oxidant …
Organocatalytic asymmetric azidation of sulfoxonium ylides: mild synthesis of enantioenriched α-azido ketones bearing a labile tertiary stereocenter
Disclosed here is a catalytic asymmetric azidation reaction for the efficient synthesis of α-
azido ketones bearing a labile tertiary stereocenter. With a superb chiral squaramide …
azido ketones bearing a labile tertiary stereocenter. With a superb chiral squaramide …
Visible light-driven azidation/difunctionalization of vinyl arenes with azidobenziodoxole under copper catalysis
D Wu, SS Cui, Y Lin, L Li, W Yu - The Journal of Organic …, 2019 - ACS Publications
Visible light-driven azidation of vinyl arenes with azidobenziodoxole as the azidating agent
was investigated in acetonitrile by using Cu (I)(phenanthroline) 2 complex [Cu (dap) 2] PF6 …
was investigated in acetonitrile by using Cu (I)(phenanthroline) 2 complex [Cu (dap) 2] PF6 …
Free Radicals in the Queue: Selective Successive Addition of Azide and N-Oxyl Radicals to Alkenes
ER Lopat'eva, IB Krylov, SA Paveliev… - The Journal of …, 2023 - ACS Publications
The selective successive addition of azide (• N3) and N-oxyl radicals to alkenes is
demonstrated, despite each of the two radicals being known to attack C═ C bonds and the …
demonstrated, despite each of the two radicals being known to attack C═ C bonds and the …