Carbodiimide-based synthesis of N-heterocycles: moving from two classical reactive sites to chemical bond breaking/forming reaction

Y Wang, WX Zhang, Z Xi - Chemical Society Reviews, 2020 - pubs.rsc.org
Carbodiimides are a unique class of heterocumulene compounds that display distinctive
chemical properties. The rich chemistry of carbodiimides has drawn increasing attention …

Ketenes and other cumulenes as reactive intermediates

AD Allen, TT Tidwell - Chemical Reviews, 2013 - ACS Publications
Reactive intermediates as recognized chemical entities date back for over a century, and
among the earliest examples were simple free radicals, as identified in 1879, when it was …

The thriving chemistry of ketenimines

P Lu, Y Wang - Chemical Society Reviews, 2012 - pubs.rsc.org
Ketenimines are an important class of reactive species and useful synthetic intermediates.
During the last two decades several practical and versatile approaches to ketenimines have …

A general method to diverse cinnolines and cinnolinium salts.

D Zhao, Q Wu, X Huang, F Song… - Chemistry-A European …, 2013 - search.ebscohost.com
Rhodium catalysis: A highly efficient and general method has been established to prepare
cinnolines, cinnolinium salts, and polycyclic cinnolinium salts through the rhodium (III) …

Catalyst-Free Cascade Annulation of Enaminones and Aryl Diazonium Tetrafluoroboronates for Cinnoline Synthesis and the Anti-Inflammatory Activity Study

S Tian, Y Liu, C Wan, JP Wan… - The Journal of Organic …, 2023 - ACS Publications
A simple and concise method for the synthesis of cinnolines has been developed by the
reactions of readily available enaminones and aryl diazonium tetrafluoroboronates. The …

Metal-Free [5+ 1] Cycloaddition–Aromatization of Benzotriazoles and Sulfur Ylides to Construct 1, 2, 4-Benzotriazines

X Wang, J Yu, M Xu, H Mao, Y Shan, X Lv… - Organic Letters, 2022 - ACS Publications
Reported herein is a novel [5+ 1] cycloaddition–aromatization of benzotriazoles and sulfur
ylides to efficiently construct 1, 2, 4-benzotriazine derivates with good yield. This new …

Rh(III)- or Ru(II)-Catalyzed C–H Annulation with Vinylene Carbonate and an Unexpected Aerobic Oxidation/Deprotection Cascade to Yield Cinnolin-4(1H)-ones

Y Wang, Y Zeng, Y Xiao, J Wang… - The Journal of Organic …, 2024 - ACS Publications
Transition metal-catalyzed C–H annulation reactions have been extensively utilized for the
synthesis of cinnolines, especially the N-protected ones; however, none of them can yield …

Reactivity for the Diels–Alder reaction of cumulenes: a distortion-interaction analysis along the reaction pathway

S Liu, Y Lei, X Qi, Y Lan - The Journal of Physical Chemistry A, 2014 - ACS Publications
Cumulenes, including allene, ketenimine, and ketene, can be employed as dienophiles in
Diels–Alder type reactions. The activation energies of a Diels–Alder reaction between …

Substrate Directed C–H Activation for the Synthesis of Benzo[c]cinnolines through a Sequential C–C and C–N Bond Formation

BVS Reddy, CR Reddy, MR Reddy, S Yarlagadda… - Organic …, 2015 - ACS Publications
A wide range of benzo [c] cinnolines are prepared through a sequential C–C and C–N bond
formation by means of an oxidative C–H functionalization. The reaction proceeds via the C …

Dynamic Covalent Chemistry: A Facile Room‐Temperature, Reversible, Diels–Alder Reaction between Anthracene Derivatives and N‐Phenyltriazolinedione

N Roy, JM Lehn - Chemistry–An Asian Journal, 2011 - Wiley Online Library
A series of readily accessible, dynamic Diels–Alder reactions that are reversible at room
temperature have been developed between anthracene derivatives as dienes and N‐phenyl …