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From 2000 to mid-2010: a fruitful decade for the synthesis of pyrazoles.

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This article is published in Chemical Reviews.The article was published on 2011-08-01. It has received 839 citations till now.

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Recyclable ZnIn2S4 Microspheres for Photocatalytic Azolation of N-Heterocycles

TL;DR: In this article , a series of zinc indium sulfide (ZnIn2S4) was synthesized by solvothermal methods in different solvents and showed the highest photocurrent density.
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Cascade and multicomponent synthesis of structurally diverse 2-(pyrazol-3-yl)pyridines and polysubstituted pyrazoles.

TL;DR: In these multicomponent reactions, complex molecules featuring three different heterocycles are assembled in a single step from commercial materials, enabling the fast generation of molecular diversity.
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Thermodynamic vs. Kinetic Control in Synthesis of O-Donor 2,5-Substituted Furan and 3,5-Substituted Pyrazole from Heteropropargyl Precursor

TL;DR: In this article , Sonogashira cross-coupling conditions of 4-tert-butylphenyl propargyl ether with benzoyl chloride followed by tandem Michael addition/cyclocondensation with hydrazine into 3,5-disubstituted pyrazole were established through a variation of the catalyst loading, solvent polarity, excess of triethylamine, and time of reaction.
References
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Journal ArticleDOI

Modern Synthetic Methods for Copper‐Mediated C(aryl) ? O, C(aryl) ? N, and C(aryl) ? S Bond Formation

TL;DR: In this article, the authors highlight the recent developments in the copper-mediated (both stoichiometric and catalytic) reactions of aryl boronic acids as reaction partners in both O- and N-arylation.
Journal ArticleDOI

Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis.

TL;DR: Using R-Hydroxy Stannanes as a Model for a Methylenation Reaction and Conclusions and Future Prospects are presented.
BookDOI

Synthetic applications of 1,3-dipolar cycloaddition chemistry toward heterocycles and natural products

TL;DR: In this paper, the authors present a list of the most important properties of Nitrones and Azomethine Ylides: Nitrones (Jason N. Martin and Raymond C. Jones), Nitronates (Scott E. Denmark and Jeromy J. Cottell), Azides (Chin-Kang Sha and A. K. Mohanakrishnan). Mesoionic Ring Systems (Gordon W. Gribble). Effect of External Reagents (Shuji Kanemasa). Asymmetric Reactions (Kurt Vesterager Gothe
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