o-Silylaryl Triflates: A Journey of Kobayashi Aryne Precursors
J Shi, L Li, Y Li - Chemical Reviews, 2021 - ACS Publications
Arynes are among the most active organic intermediates and have found numerous
applications in expeditious preparation of substituted arenes. In the past 20 years, chemists …
applications in expeditious preparation of substituted arenes. In the past 20 years, chemists …
Recent advances in molecular rearrangements involving aryne intermediates
This Feature Article is aimed at highlighting the recent developments in the transition-metal-
free molecular rearrangements involving arynes. The chemistry of arynes has shown …
free molecular rearrangements involving arynes. The chemistry of arynes has shown …
The role of aryne distortions, steric effects, and charges in regioselectivities of aryne reactions
JM Medina, JL Mackey, NK Garg… - Journal of the American …, 2014 - ACS Publications
The distortion/interaction model has been used to explain and predict reactivity in a variety
of reactions where more common explanations, such as steric and electronic factors, do not …
of reactions where more common explanations, such as steric and electronic factors, do not …
Halogenated metal–organic framework glasses and liquids
J Hou, ML Rios Gomez, A Krajnc… - Journal of the …, 2020 - ACS Publications
The synthesis of four novel crystalline zeolitic imidazolate framework (ZIF) structures using a
mixed-ligand approach is reported. The inclusion of both imidazolate and halogenated …
mixed-ligand approach is reported. The inclusion of both imidazolate and halogenated …
Recent applications of aryne chemistry to organic synthesis. A review
R Sanz - Organic Preparations and Procedures International, 2008 - Taylor & Francis
Arynes are neutral intermediates in which two adjacent atoms of an aromatic ring lack
substituents, thus leaving two atomic orbitals (perpendicular to the aromatic x system) to …
substituents, thus leaving two atomic orbitals (perpendicular to the aromatic x system) to …
Facile N-Arylation of Amines and Sulfonamides and O-Arylation of Phenols and Arenecarboxylic Acids
Z Liu, RC Larock - The Journal of organic chemistry, 2006 - ACS Publications
An efficient, transition-metal-free procedure for the N-arylation of amines, sulfonamides, and
carbamates and O-arylation of phenols and carboxylic acids has been achieved by allowing …
carbamates and O-arylation of phenols and carboxylic acids has been achieved by allowing …
Diaryl hypervalent bromines and chlorines: synthesis, structures and reactivities
M Lanzi, J Wencel-Delord - Chemical Science, 2024 - pubs.rsc.org
In the field of modern organic chemistry, hypervalent compounds have become
indispensable tools for synthetic chemists, finding widespread applications in both academic …
indispensable tools for synthetic chemists, finding widespread applications in both academic …
Benzyne click chemistry: synthesis of benzotriazoles from benzynes and azides
F Shi, JP Waldo, Y Chen, RC Larock - Organic letters, 2008 - ACS Publications
Benzyne Click Chemistry: Synthesis of Benzotriazoles from Benzynes and Azides | Organic
Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS …
Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS …
Cyclic Diaryl λ3‐Bromanes as Original Aryne Precursors
M Lanzi, Q Dherbassy… - Angewandte Chemie …, 2021 - Wiley Online Library
Despite the widespread application of hypervalent iodines, the corresponding λ3‐bromanes
are less explored. Herein we report a general, safe, and high‐yielding strategy to access …
are less explored. Herein we report a general, safe, and high‐yielding strategy to access …
Synthesis of Spiro[4.5]trienones by Intramolecular ipso-Halocyclization of 4-(p-Methoxyaryl)-1-alkynes
X Zhang, RC Larock - Journal of the American Chemical Society, 2005 - ACS Publications
A wide variety of 3-halospiro [4.5] trienones are readily prepared in good to excellent yields
by the intramolecular ipso-halocyclization of 4-(p-methoxyaryl)-1-alkynes under mild …
by the intramolecular ipso-halocyclization of 4-(p-methoxyaryl)-1-alkynes under mild …