Solventless Reactions (SLR)

2006 ◽  
pp. 53-87 ◽  
Author(s):  
Rajender S. Varma ◽  
Yuhong Ju
Keyword(s):  
Solventless Reactions

Solventless Reactions of 5(4H)-Oxazolones with Umbelliferones and Selected Enolcarbonyl Compounds.

ChemInform ◽  
2004 ◽  
Vol 35 (2) ◽  
Author(s):  
Massimiliano Cordaro ◽  
Leonardo Di Donna ◽  
Francesco Foti ◽  
Giovanni Grassi ◽  
Anna Napoli ◽  
...  
Keyword(s):  
Solventless Reactions

Solventless Reactions of 5(4H)-Oxazolones with Umbelliferones andSelected Enolcarbonyl Compounds

Synlett ◽  
2003 ◽  
pp. 1710-1712
Author(s):  
Giovanni Grassi ◽  
Massimiliano Cordaro ◽  
Leonardo Di Donna ◽  
Francesco Foti ◽  
Anna Napoli ◽  
...  
Keyword(s):  
Solventless Reactions

ChemInform Abstract: Solventless Reactions

ChemInform ◽  
2008 ◽  
Vol 39 (35) ◽  
Author(s):  
Rajender S. Varma ◽  
Yuhong Ju
Keyword(s):  
Solventless Reactions

Solventless Reactions for the Synthesis of Organotin Clusters and Cages§

2003 ◽  
Vol 22 (18) ◽  
pp. 3710-3716 ◽  
Author(s):  
Vadapalli Chandrasekhar ◽  
Viswanathan Baskar ◽  
Ramamoorthy Boomishankar ◽  
Kandasamy Gopal ◽  
Stefano Zacchini ◽  
...  
Keyword(s):  
Solventless Reactions

Behaviour of iprit carbonate analogues in solventless reactions

RSC Advances ◽  
2014 ◽  
Vol 4 (59) ◽  
pp. 31071-31078 ◽  
Author(s):  
F. Arico' ◽  
S. Evaristo ◽  
P. Tundo
Keyword(s):  
Nucleophilic Substitution ◽  
Atmospheric Pressure ◽  
Catalytic Amount ◽  
Solventless Reactions

Sulfur iprit carbonate analogues showed to undergo nucleophilic substitution with several substrates in neat conditions at atmospheric pressure, in the presence and in the absence of a catalytic amount of base.

Can Solventless Reactions Sometimes Succeed When Solvent-Mediated Reactions Fail? A Second Case Study for Cu(I) and Ag(I) Complexes of Divergently Bridging Diimines without or with Fluorinated Azolates

2020 ◽  
Vol 40 (6) ◽  
pp. 277-303
Author(s):  
Ruaa M. Almotawa ◽  
Christopher Hu ◽  
Alessandro Cimino ◽  
Vladimir N. Nesterov ◽  
Mohammad A. Omary ◽  
...  
Keyword(s):  
Solventless Reactions

scholarly journals Microwave Irradiation: Alternative Heating Process for the Synthesis of Biologically Applicable Chromones, Quinolones, and Their Precursors

Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6293
Author(s):  
Hélio M. T. Albuquerque ◽  
Diana C. G. A. Pinto ◽  
Artur M. S. Silva
Keyword(s):  
Energy Consumption ◽  
Microwave Irradiation ◽  
Organic Synthesis ◽  
Heterocyclic Compounds ◽  
Reaction Times ◽  
Heating Process ◽  
Research Groups ◽  
Heating Source ◽  
Microwave Assisted ◽  
Solventless Reactions

Microwave irradiation has become a popular heating technique in organic synthesis, mainly due to its short reaction times, solventless reactions, and, sometimes, higher yields. Additionally, microwave irradiation lowers energy consumption and, consequently, is ideal for optimization processes. Moreover, there is evidence that microwave irradiation can improve the regioselectivity and stereoselectivity aspects of vital importance in synthesizing bioactive compounds. These crucial features of microwave irradiation contribute to its inclusion in green chemistry procedures. Since 2003, the use of microwave-assisted organic synthesis has become common in our laboratory, making our group one of the first Portuguese research groups to implement this heating source in organic synthesis. Our achievements in the transformation of heterocyclic compounds, such as (E/Z)-3-styryl-4H-chromen-4-ones, (E)-3-(2-hydroxyphenyl)-4-styryl-1H-pyrazole, (E)-2-(4-arylbut-1-en-3-yn-1-yl)-4H-chromen-4-ones, or (E)-2-[2-(5-aryl-2-methyl-2H-1,2,3-triazol-4-yl)vinyl]-4H-chromen-4-ones, will be discussed in this review, highlighting the benefits of microwave irradiation use in organic synthesis.

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