ChemInform Abstract: One-Pot Synthesis of Functionalized Isoxazole-Thiolane Hybrids via Knoevenagel Condensation and Domino Sulfa-1,6-Michael/Intramolecular Vinylogous Henry Reactions.

ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Sakkani Nagaraju ◽  
Neeli Satyanarayana ◽  
Banoth Paplal ◽  
Anuji K. Vasu ◽  
Sriram Kanvah ◽  
...  
Keyword(s):  
Knoevenagel Condensation ◽  
One Pot ◽  
One Pot Synthesis

scholarly journals ZnO nanoparticle as catalyst for efficient green one-pot synthesis of coumarins through Knoevenagel condensation

2011 ◽  
Vol 123 (5) ◽  
pp. 615-621 ◽  
Author(s):  
B VINAY KUMAR ◽  
HALEHATTY S BHOJYA NAIK ◽  
D GIRIJA ◽  
B VIJAYA KUMAR
Keyword(s):  
Knoevenagel Condensation ◽  
Zno Nanoparticle ◽  
One Pot ◽  
One Pot Synthesis

New Syntheses of 3-Aroylflavone Derivatives; Knoevenagel Condensation and Oxidation versus One-Pot Synthesis

Synlett ◽  
2012 ◽  
Vol 23 (16) ◽  
pp. 2353-2356 ◽  
Author(s):  
Diana Pinto ◽  
Artur Silva ◽  
Patrícia Vaz ◽  
Djenisa Rocha ◽  
José Cavaleiro
Keyword(s):  
Knoevenagel Condensation ◽  
One Pot ◽  
One Pot Synthesis

One-pot synthesis of functionalized isoxazole–thiolane hybrids via Knoevenagel condensation and domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactions

RSC Advances ◽  
2015 ◽  
Vol 5 (114) ◽  
pp. 94474-94478 ◽  
Author(s):  
Sakkani Nagaraju ◽  
Neeli Satyanarayana ◽  
Banoth Paplal ◽  
Anuji K. Vasu ◽  
Sriram Kanvah ◽  
...  
Keyword(s):  
Reaction Time ◽  
Knoevenagel Condensation ◽  
One Pot ◽  
One Pot Synthesis

One-pot synthesis of isoxazole–thiolane hybrids are reported via the Knoevenagel condensation, domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactions using piperidine (30 mol%) with >95% yields in 2–2.5 h overall reaction time.

scholarly journals Microwave-Assisted Three-Component “Catalyst and Solvent-Free” Green Protocol: A Highly Efficient and Clean One-Pot Synthesis of Tetrahydrobenzo[b]pyrans

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Sougata Santra ◽  
Matiur Rahman ◽  
Anupam Roy ◽  
Adinath Majee ◽  
Alakananda Hajra
Keyword(s):  
Knoevenagel Condensation ◽  
One Pot ◽  
Green Protocol ◽  
Microwave Assisted ◽  
Highly Efficient ◽  
One Pot Synthesis ◽  
Purification Technique ◽  
The One ◽  
High Yields ◽  
Operational Simplicity

A green and highly efficient method has been developed for the one-pot synthesis of tetrahydrobenzo[b]pyrans via a three-component condensation of aldehydes, 1,3-cyclic diketones, and malononitrile under MW irradiation without using any catalyst and solvent. This transformation presumably occurs by a sequential Knoevenagel condensation, Michael addition, and intramolecular cyclization. Operational simplicity, solvent and catalyst-free conditions, the compatibility with various functional groups, nonchromatographic purification technique, and high yields are the notable advantages of this procedure.

Tandem one-pot synthesis of flavans by recyclable silica–HClO4 catalyzed Knoevenagel condensation and [4 + 2]-Diels–Alder cycloaddition

2012 ◽  
Vol 10 (26) ◽  
pp. 5143 ◽  
Author(s):  
Sandip B. Bharate ◽  
Ramesh Mudududdla ◽  
Jaideep B. Bharate ◽  
Narsaiah Battini ◽  
Satyanarayana Battula ◽  
...  
Keyword(s):  
Knoevenagel Condensation ◽  
Diels Alder ◽  
One Pot ◽  
One Pot Synthesis
Sign in / Sign up

Export Citation Format

Share Document