The Heck reaction as a sharpening stone of palladium catalysis

IP Beletskaya, AV Cheprakov - Chemical Reviews, 2000 - ACS Publications
Palladium catalysis has achieved the status of an indispensable tool for both common and
state-of-theart organic synthesis. Among basic types of palladium-catalyzed transformations …

Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions

FX Felpin, S Sengupta - Chemical Society Reviews, 2019 - pubs.rsc.org
The rich legacy of arenediazonium salts in the synthesis of unsymmetrical biaryls, built
around the seminal works of Pschorr, Gomberg and Bachmann more than a century ago …

Triazenes: a versatile tool in organic synthesis

DB Kimball, MM Haley - Angewandte Chemie International …, 2002 - Wiley Online Library
Abstract Triazenes (RN N NR′ R ″) are a class of compounds that hold much promise
in preparative chemistry as they are reactive groups which are both stable and adaptable to …

Recent advances in the Heck–Matsuda reaction in heterocyclic chemistry

FX Felpin, L Nassar-Hardy, F Le Callonnec, E Fouquet - Tetrahedron, 2011 - Elsevier
This review summarizes the recent advances made in the last ten years on Heck–Matsuda
couplings, involving aryl diazonium salts, in heterocyclic chemistry including natural …

Using aryl diazonium salts in palladium-catalyzed reactions under safer conditions

N Oger, M d'Halluin, E Le Grognec… - … Process Research & …, 2014 - ACS Publications
In this review, we give a concise but complete overview of methods describing the use of
aryl diazonium salts in palladium-catalyzed reactions under safe conditions from a …

Comparison of the thermal stabilities of diazonium salts and their corresponding triazenes

C Schotten, SK Leprevost, LM Yong… - … Process Research & …, 2020 - ACS Publications
A range of diazonium salts and their corresponding triazenes have been prepared in order
to directly compare their relative thermal stabilities (via initial decomposition temperature) …

Recent advances in the chemistry of aryltriazene

T Liu, H Wu, Q Zhang, C Wang - Organic & Biomolecular Chemistry, 2023 - pubs.rsc.org
Triazene is one of the most versatile building blocks in organic synthesis. Generally, it is
viewed as a safe equivalent of diazonium salt, thus immediately finding numerous …

Boron trifluoride induced palladium-catalyzed cross-coupling reaction of 1-aryltriazenes with areneboronic acids

T Saeki, EC Son, K Tamao - Organic Letters, 2004 - ACS Publications
Aryltriazenes are directly coupled with areneboronic acids in the presence of a catalytic
amount of Pd2 (dba) 3 and P (t Bu) 3 together with 1 equiv of BF3⊙ OEt2 in DME to afford …

Cyclization of 1-(2-alkynylphenyl)-3, 3-dialkyltriazenes: a convenient, high-yield synthesis of substituted cinnolines and isoindazoles

DB Kimball, TJR Weakley… - The Journal of Organic …, 2002 - ACS Publications
A new route to isoindazoles and cinnolines through the cyclization of (2-alkynylphenyl)
triazenes under neutral conditions is presented. The products that result from heating the …

1‐Aryltriazenes in the Suzuki, Heck, and Sonogashira Reactions in Imidazolium‐ILs, with [BMIM(SO3H)][OTf] or Sc(OTf)3 as Promoter, and Pd(OAc)2 or NiCl2 …

SM Sutar, HM Savanur, SS Malunavar… - European Journal of …, 2019 - Wiley Online Library
1‐Aryltriazenes, the protected and more stable form of aryl‐diazonium species, can be
conveniently unmasked with Brønsted acidic‐IL or Sc (OTf) 3 and coupled with a host of …