Piper-Betle-Shaped Nano-S-Catalyzed Synthesis of 1-Amidoalkyl-2-naphthols under Solvent-Free Reaction Condition: A Greener “Nanoparticle-Catalyzed Organic Synthesis Enhancement” Approach

2013 ◽  
Vol 78 (7) ◽  
pp. 3361-3366 ◽  
Author(s):  
Vijay K. Das ◽  
Madhurjya Borah ◽  
Ashim J. Thakur
Keyword(s):  
Organic Synthesis ◽  
Solvent Free ◽  
Piper Betle ◽  
Reaction Condition ◽  
Solvent Free Reaction

scholarly journals Nanorod-Shaped Basic Al2O3 Catalyzed N,N-Diformylation of Bisuracil Derivatives: A Greener “NOSE” Approach

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Vijay K. Das ◽  
Ashim J. Thakur
Keyword(s):  
Organic Synthesis ◽  
Recyclable Catalyst ◽  
Solvent Free ◽  
Reaction Condition ◽  
Solvent Free Reaction

A feasible “NOSE” (nanoparticles-catalyzed organic synthesis enhancement) protocol has been developed for N,N-diformylation of bisuracil derivatives using nano-Al2O3 rods as an efficient, inexpensive, and recyclable catalyst under solvent-free reaction condition at 40°C. The catalyst was reused up to the 4th cycle without affecting the rate and yield of the N,N-diformylation products appreciably.

scholarly journals Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions

Molecules ◽  
2020 ◽  
Vol 25 (16) ◽  
pp. 3579
Author(s):  
Claudia Gabriela Avila-Ortiz ◽  
Eusebio Juaristi
Keyword(s):  
Organic Synthesis ◽  
Additional Condition ◽  
Mechanochemical Activation ◽  
Chemical Activation ◽  
Point Of View ◽  
Solvent Free ◽  
Chemical Transformations ◽  
Atom Economy ◽  
Reaction Conditions ◽  
Solvent Free Reaction

One central challenge for XXI century chemists is the development of sustainable processes that do not represent a risk either to humanity or to the environment. In this regard, the search for more efficient and clean alternatives to achieve the chemical activation of molecules involved in chemical transformations has played a prominent role in recent years. The use of microwave or UV-Vis light irradiation, and mechanochemical activation is already widespread in many laboratories. Nevertheless, an additional condition to achieve “green” processes comes from the point of view of so-called atom economy. The removal of solvents from chemical reactions generally leads to cleaner, more efficient and more economical processes. This review presents several illustrative applications of the use of sustainable protocols in the synthesis of organic compounds under solvent-free reaction conditions.

One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions

2020 ◽  
Vol 17 (6) ◽  
pp. 438-442
Author(s):  
Xiaofang Ma ◽  
Shunxi Li ◽  
Samrat Devaramani ◽  
Guohu Zhao ◽  
Daqian Xu
Keyword(s):  
Reaction Time ◽  
Organic Synthesis ◽  
Carbonyl Compounds ◽  
Solvent Free ◽  
Propargyl Bromide ◽  
Important Goal ◽  
One Pot ◽  
Short Reaction Time ◽  
Solvent Free Conditions ◽  
Volatile Organic

The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.

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