Multicomponent one-pot synthesis of highly-functionalized pyrrole-3-carbonitriles in aqueous medium and their computational study

2015 ◽  
Vol 13 (6) ◽  
pp. 1800-1806 ◽  
Author(s):  
Ramakanth Pagadala ◽  
Devendar Reddy Kommidi ◽  
Shravankumar Kankala ◽  
Suresh Maddila ◽  
Parvesh Singh ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Computational Study ◽  
One Pot ◽  
One Pot Synthesis

A one-pot protocol involving four-components in water is developed to synthesize functionalized pyrroles.

ChemInform Abstract: Multicomponent One-Pot Synthesis of Highly-Functionalized Pyrrole-3-carbonitriles in Aqueous Medium and Their Computational Study.

ChemInform ◽  
2015 ◽  
Vol 46 (25) ◽  
pp. no-no
Author(s):  
Ramakanth Pagadala ◽  
Devendar Reddy Kommidi ◽  
Shravankumar Kankala ◽  
Suresh Maddila ◽  
Parvesh Singh ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Computational Study ◽  
One Pot ◽  
One Pot Synthesis

ChemInform Abstract: Nanodomain Cubic Cuprous Oxide as Reusable Catalyst in One-Pot Synthesis of 3-Alkyl/Aryl-3- (pyrrole-2-yl/indole-3-yl)-2-phenyl-2,3-dihydro-isoindolinones in Aqueous Medium.

ChemInform ◽  
2014 ◽  
Vol 45 (41) ◽  
pp. no-no
Author(s):  
Swarbhanu Sarkar ◽  
Nivedita Chatterjee ◽  
Manas Roy ◽  
Rammyani Pal ◽  
Sabyasachi Sarkar ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Cuprous Oxide ◽  
Reusable Catalyst ◽  
One Pot ◽  
Alkyl Aryl ◽  
One Pot Synthesis

scholarly journals A rare γ-pyranopyrazole skeleton: design, one-pot synthesis and computational study

2016 ◽  
Vol 14 (31) ◽  
pp. 7490-7494 ◽  
Author(s):  
Muhammed Üçüncü ◽  
Ceren Cantürk ◽  
Erman Karakuş ◽  
Hüseyin Zeybek ◽  
Uğur Bozkaya ◽  
...  
Keyword(s):  
Computational Study ◽  
Synthetic Method ◽  
One Pot ◽  
One Pot Synthesis

A base mediated one-pot, two-step synthetic method for constructing γ-pyranopyrazoles.

Hydrophilic Pd-phosphines catalyzed one-pot synthesis of substituted isoquinolines, furopyridines and thienopyridines in aqueous medium

2019 ◽  
Vol 60 (3) ◽  
pp. 297-299 ◽  
Author(s):  
Veeranna Guguloth ◽  
Narasimha Swamy Thirukovela ◽  
Ramesh Balaboina ◽  
Suresh Paidakula ◽  
Ravinder Vadde
Keyword(s):  
Aqueous Medium ◽  
One Pot ◽  
One Pot Synthesis

One-Pot Synthesis of Nucleotides and Conjugates in Aqueous Medium

2016 ◽  
Vol 2017 (2) ◽  
pp. 241-245 ◽  
Author(s):  
Anaïs Depaix ◽  
Suzanne Peyrottes ◽  
Béatrice Roy
Keyword(s):  
Aqueous Medium ◽  
One Pot ◽  
One Pot Synthesis

Using a traceless directing group for the silver-mediated synthesis of 3-trifluoromethylpyrazoles: a computational study on the mechanism and origins of regioselectivity

2018 ◽  
Vol 5 (23) ◽  
pp. 3374-3381 ◽  
Author(s):  
Feiyun Jia ◽  
Jiewei Luo ◽  
Bo Zhang
Keyword(s):  
Density Functional Theory ◽  
Dft Calculations ◽  
Density Functional ◽  
Computational Study ◽  
One Pot ◽  
Functional Theory ◽  
One Pot Synthesis ◽  
Directing Group

The silver-mediated one-pot synthesis of 3-trifluoromethylpyrazoles using a traceless directing group was investigated by density functional theory (DFT) calculations.

Alum (KAl(SO4)2·12H2O)-Catalyzed, Eco-Friendly, and Efficient One-Pot Synthesis of 2-Arylbenzothiazoles and 2-Arylbenzoxazole in Aqueous Medium

2008 ◽  
Vol 61 (11) ◽  
pp. 905 ◽  
Author(s):  
Shivaji S. Pawar ◽  
Deepak V. Dekhane ◽  
Murlidhar S. Shingare ◽  
Shivaji N. Thore
Keyword(s):  
Ambient Temperature ◽  
Aqueous Medium ◽  
Simple Procedure ◽  
Reaction Yield ◽  
One Pot ◽  
Mild Conditions ◽  
One Pot Synthesis ◽  
Novel Catalyst

Alum (KAl(SO4)2·12H2O) performs as a novel catalyst for the synthesis of 2-arylbenzothiazoles and 2-arylbenzoxazole from o-aminothiophenol and o-aminophenol with various substituted aldehydes in good to excellent isolated yields (85–95%) using water as a solvent at ambient temperature. Several solvents were examined for this reaction; however, in terms of reaction yield and time, water was found to be the optimum solvent. The remarkable advantages offered by this method are an inexpensive and easily available catalyst, a simple procedure, mild conditions, much faster (60–90 min) reactions, and good to excellent yields of products.

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