ChemInform Abstract: Microwave-Assisted Synthesis of Indole-Annulated Dihydropyrano[3,4-c]chromene Derivatives via Hetero-Diels-Alder Reaction.

ChemInform ◽  
2011 ◽  
Vol 42 (48) ◽  
pp. no-no
Author(s):  
Mukund Jha ◽  
Stephanie Guy ◽  
Ting-Yi Chou
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted Synthesis ◽  
Microwave Assisted ◽  
Diels Alder Reaction

Microwave-Assisted Synthesis of Camphor-Derived Chiral Imidazolium Ionic Liquids and Their Application in Diastereoselective Diels-Alder Reaction

Synthesis ◽  
2007 ◽  
Vol 2007 (9) ◽  
pp. 1333-1338 ◽  
Author(s):  
Peter Gaertner ◽  
Katharina Bica ◽  
Guenter Gmeiner ◽  
Christian Reichel ◽  
Bernhard Lendl
Keyword(s):  
Ionic Liquids ◽  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted Synthesis ◽  
Imidazolium Ionic Liquids ◽  
Microwave Assisted ◽  
Diels Alder Reaction

Extensive methodology screening of meso-tetrakys-(furan-2-yl)-porphyrin microwave-assisted synthesis

2016 ◽  
Vol 40 (3) ◽  
pp. 2574-2581 ◽  
Author(s):  
Federica Bosca ◽  
Silvia Tagliapietra ◽  
Claudio Garino ◽  
Giancarlo Cravotto ◽  
Alessandro Barge
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted Synthesis ◽  
Microwave Assisted ◽  
Diels Alder Reaction ◽  
One Step ◽  
Fast Procedure

meso-Tetrakys-(furan-2-yl)-porphyrin has been prepared by a one step, microwave assisted, fast procedure. The Diels–Alder reaction is proposed to further decorate the porphyrin scaffold.

ChemInform Abstract: Microwave-Assisted Diels-Alder Reaction Supported on Graphite.

ChemInform ◽  
2010 ◽  
Vol 27 (38) ◽  
pp. no-no
Author(s):  
B. GARRIGUES ◽  
C. LAPORTE ◽  
R. LAURENT ◽  
A. LAPORTERIE ◽  
J. DUBAC
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted ◽  
Diels Alder Reaction

Microwave-Assisted Intramolecular Diels-Alder Reaction towards the Total Synthesis of Symbioimine

Synlett ◽  
2008 ◽  
Vol 2008 (18) ◽  
pp. 2877-2881 ◽  
Author(s):  
Yoshihisa Kobayashi ◽  
Stephen Born ◽  
Genesis Bacani ◽  
Erin Olson
Keyword(s):  
Total Synthesis ◽  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted ◽  
Diels Alder Reaction

Microwave-assisted Diels-Alder synthesis

2001 ◽  
Vol 79 (12) ◽  
pp. 1906-1909 ◽  
Author(s):  
Christopher K Jankowski ◽  
Gaëtan LeClair ◽  
Jacqueline MR Bélanger ◽  
Jocelyn RJ Paré ◽  
Marie-Rose VanCalsteren
Keyword(s):  
High Resolution ◽  
Microwave Synthesis ◽  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Method ◽  
Diene Synthesis ◽  
Microwave Assisted ◽  
Diels Alder Reaction ◽  
Pyridine Carboxylate ◽  
Danishefsky's Diene

The synthesis of isoquinolinone carboxylates was performed using arecoline or its isomer N-methyl tetrahydro pyridine carboxylate with Danishefsky's diene via thermal or microwave assisted Diels-Alder reaction. The comparison of both condensation modes showed that the microwave method not only afforded higher yields of the adducts, but also lead to the formation of a new α,β-unsaturated pyridyl ketone. All structures were identified with the help of high resolution 2D NMR.Key words: Diels-Alder microwave assisted reaction, microwave synthesis, Michael, diene, isoquinoline carboxylate synthesis, Danishefsky diene synthesis, MAP Diels-Alder2.

Microwave-assisted Diels–Alder reaction of 1,3,3-trimethyl-2-vinyl-1-cyclohexene with chromones — An expeditious approach to analogues of the puupehenone group of marine diterpenoids and kampanols

2010 ◽  
Vol 88 (12) ◽  
pp. 1233-1239 ◽  
Author(s):  
Rajesh M. Kamble ◽  
M. M.V. Ramana
Keyword(s):  
Microwave Irradiation ◽  
Alder Reaction ◽  
Diels Alder ◽  
Microwave Assisted ◽  
Diels Alder Reaction ◽  
Tetracyclic Core

A rapid assembly of the tetracyclic core of marine diterpenoids related to puupehenone and kampanols by a Diels–Alder reaction of 1,3,3-trimethyl-2-vinyl-1-cyclohexene with chromones under microwave irradiation with or without TiCl4 is described.

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