An expedient microwave-assisted, solvent-free, solid-supported synthesis of pyrrolo[2,3-d]pyrimidine-pyrano[5,6-c]coumarin/[6,5-c]chromone derivatives by intramolecular hetero Diels–Alder reaction

Tetrahedron Letters ◽

10.1016/j.tetlet.2008.01.059 ◽

2008 ◽

Vol 49 (11) ◽

pp. 1812-1817 ◽

Author(s):

Ekambaram Ramesh ◽

Raghavachary Raghunathan

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Chromone Derivatives ◽

Microwave Assisted ◽

Diels Alder Reaction

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ChemInform Abstract: An Expedient Microwave-Assisted, Solvent-Free, Solid-Supported Synthesis of Pyrrolo[2,3-d]pyrimidine-pyrano[5,6-c]coumarin/[6,5-c]chromone Derivatives by Intramolecular hetero Diels-Alder Reaction.

10.1002/chin.200826164 ◽

2008 ◽

Vol 39 (26) ◽

Author(s):

Ekambaram Ramesh ◽

Raghavachary Raghunathan

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Chromone Derivatives ◽

Microwave Assisted ◽

Diels Alder Reaction

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ChemInform Abstract: Microwave-Assisted Efficient Synthesis of Spiroquinoline Derivatives via a Catalyst- and Solvent-Free Aza-Diels-Alder Reaction.

10.1002/chin.201312142 ◽

2013 ◽

Vol 44 (12) ◽

pp. no-no

Author(s):

Debajyoti Bhuyan ◽

Rupam Sarma ◽

Dipak Prajapati

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Efficient Synthesis ◽

Microwave Assisted ◽

Diels Alder Reaction

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Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes

Synthesis ◽

10.1055/s-0031-1289610 ◽

2011 ◽

Vol 2011 (24) ◽

pp. 4077-4083 ◽

Author(s):

Radim Nencka ◽

Milan Dejmek ◽

Hubert Hřebabecký ◽

Michal Šála ◽

Martin Dračínský

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Simple Route ◽

Microwave Assisted ◽

Diels Alder Reaction

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Microwave-Assisted Solvent-Free Diels-Alder Reaction - A Fast and Simple Route to Various 5,6-Substituted Norbornenes and Polychlorinated Norbornenes

Synthesis ◽

10.1055/s-0031-1289624 ◽

2011 ◽

Vol 2011 (24) ◽

pp. e4-e4

Author(s):

Radim Nencka ◽

Milan Dejmek ◽

Hubert Hřebabecký ◽

Michal Šála ◽

Martin Dračínský

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Simple Route ◽

Microwave Assisted ◽

Diels Alder Reaction

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MICROWAVE ASSISTED CATALYST AND SOLVENT FREE EFFICIENT SYNTHESIS OF QUINOLINE DERIVATIVES BY THREE COMPONENT ONE POT AZA-DIELS-ALDER REACTION STRATEGY

RASAYAN Journal of Chemistry ◽

10.31788/rjc.2021.1426216 ◽

2021 ◽

Vol 14 (02) ◽

pp. 887-892

Author(s):

Debajyoti Bhuyan

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Quinoline Derivatives ◽

Efficient Synthesis ◽

One Pot ◽

Microwave Assisted ◽

Diels Alder Reaction

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Microwave-assisted efficient synthesis of spiroquinoline derivatives via a catalyst- and solvent-free aza-Diels–Alder reaction

Tetrahedron Letters ◽

10.1016/j.tetlet.2012.09.081 ◽

2012 ◽

Vol 53 (47) ◽

pp. 6460-6463 ◽

Author(s):

Debajyoti Bhuyan ◽

Rupam Sarma ◽

Dipak Prajapati

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Efficient Synthesis ◽

Microwave Assisted ◽

Diels Alder Reaction

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Naphthalenes by Microwave-Assisted Dehydrogenative Diels–Alder Reaction

Synfacts ◽

10.1055/s-0032-1317441 ◽

2012 ◽

Vol 8 (11) ◽

pp. 1199-1199

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Microwave Assisted ◽

Diels Alder Reaction

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ChemInform Abstract: Microwave-Promoted Efficient Synthesis of Spiroindenotetrahydropyridine Derivatives via a Catalyst- and Solvent-Free Pseudo One-Pot Five-Component Tandem Knoevenagel/Aza-Diels-Alder Reaction.

10.1002/chin.201508153 ◽

2015 ◽

Vol 46 (8) ◽

pp. no-no

Author(s):

Debajyoti Bhuyan ◽

Manas M. Sarmah ◽

Yuvaraj Dommaraju ◽

Dipak Prajapati

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Efficient Synthesis ◽

One Pot ◽

Diels Alder Reaction

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Diels—Alder Reaction of Thiophene: Dramatic Effects of High-Pressure/Solvent-Free Conditions.

10.1002/chin.200430037 ◽

2004 ◽

Vol 35 (30) ◽

Author(s):

Koji Kumamoto ◽

Isao Fukada ◽

Hiyoshizo Kotsuki

Keyword(s):

High Pressure ◽

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Diels Alder Reaction ◽

Solvent Free Conditions

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Mechanochemical milling promoted solvent-free imino Diels–Alder reaction catalyzed by FeCl3: diastereoselective synthesis of cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines

RSC Advances ◽

10.1039/c4ra05252h ◽

2014 ◽

Vol 4 (67) ◽

pp. 35635-35638 ◽

Author(s):

Ya-Jun Tan ◽

Ze Zhang ◽

Fang-Jian Wang ◽

Hao-Hao Wu ◽

Qing-Hai Li

Keyword(s):

Ball Milling ◽

Alder Reaction ◽

Diels Alder ◽

Solvent Free ◽

Diastereoselective Synthesis ◽

Diels Alder Reaction ◽

Mechanochemical Milling

Cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines were diastereoselectively synthesized by FeCl3-promoted solvent-free Diels–Alder reaction of in situ generated imine with styrene under ball milling.

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