Application of Vinyl Azides in Chemical Synthesis: A Recent Update | The Journal of Organic Chemistry
Application of Vinyl Azides in Chemical Synthesis: A Recent Update | The Journal of Organic Chemistry
Scandium (III)‐Catalyzed Cycloaddition of in situ Generated ortho‐Quinone Methides with Vinyl Azides: An Efficient Access to Substituted 4H‐Chromenes - Thirupathi - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
vinyl azide | Organic Chemistry Periodically
Synthesis of <i>β</i>-Sulfonyl Enamines via Iodine-Catalyzed Reaction between Vinyl Azides and Sodium Arylsulfinates
Molecules | Free Full-Text | Electrochemically Induced Synthesis of Imidazoles from Vinyl Azides and Benzyl Amines
Recent Advances of <em>α</em>-Aryl Vinyl Azides in Nitrogen Heterocycle Synthesis
Metal‐Free Electrochemical Coupling of Vinyl Azides: Synthesis of Phenanthridines and β‐Ketosulfones - Li - 2020 - European Journal of Organic Chemistry - Wiley Online Library
Vinyl azide synthesis by azidonation, azidation or substitution
A hidden side of azides | amphoteros
Divergent synthesis of chiral cyclic azides via asymmetric cycloaddition reactions of vinyl azides | Nature Communications
α-Substituted vinyl azides: an emerging functionalized alkene - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00017K
Synthesis of 2,3,4-trisubstituted pyrroles via a facile reaction of vinyl azides and tosylmethyl isocyanide
BJOC - Multistep flow synthesis of vinyl azides and their use in the copper-catalyzed Huisgen-type cycloaddition under inductive-heating conditions
Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis. - Abstract - Europe PMC
Application of Vinyl Azides in Chemical Synthesis: A Recent Update | The Journal of Organic Chemistry
Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C5OB00099H
Vinyl azide | C2H3N3 - PubChem
![PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ad4e62b83576af821a221a0a20bd8ad9ee8a9ff9/2-Table1-1.png "PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar")
PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar
Scheme 74. Cycloaddition Reactions of Vinyl Azides for the Synthesis of... | Download Scientific Diagram
![PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/ad4e62b83576af821a221a0a20bd8ad9ee8a9ff9/1-Figure1-1.png "PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar")
PDF] Radical Enamination of Vinyl Azides: Direct Synthesis of N-Unprotected Enamines. | Semantic Scholar
Scheme 53. Isolation of the vinyl azide intermediate and further... | Download Scientific Diagram
Ni-Catalyzed asymmetric hetero-Diels–Alder reactions of conjugated vinyl azides: synthesis of chiral azido polycycles - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D0QO01597K
A bench-stable low-molecular-weight vinyl azide surrogate for a cascade reaction: facile access to novel N-vinyl-1,2,3-triazoles - ScienceDirect
Application of Vinyl Azides in Chemical Synthesis: A Recent Update | The Journal of Organic Chemistry
Reactivities of vinyl azides and their recent applications in nitrogen heterocycle synthesis - Organic & Biomolecular Chemistry (RSC Publishing)
![Formal [4+2]‐Annulation of Vinyl Azides with N‐Unsaturated Aldimines - Zhu - 2014 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/0aa426d1-2d8f-4238-9373-2604080ae4b5/msch001.jpg "Formal [4+2]‐Annulation of Vinyl Azides with N‐Unsaturated Aldimines - Zhu - 2014 - Chemistry – An Asian Journal - Wiley Online Library")
Formal [4+2]‐Annulation of Vinyl Azides with N‐Unsaturated Aldimines - Zhu - 2014 - Chemistry – An Asian Journal - Wiley Online Library
Synthesis of 2,3,4-trisubstituted pyrroles via a facile reaction of vinyl azides and tosylmethyl isocyanide
