From Enantiopure Hydroxyaldehydes to Complex Heterocyclic Scaffolds: Development of Domino Petasis/Diels-Alder and Cross-Metathesis/Michael Addition Reactions

2014 ◽  
Vol 20 (38) ◽  
pp. 12133-12143 ◽  
Author(s):  
Alexandre Cannillo ◽  
Stéphanie Norsikian ◽  
Marie-Elise Tran Huu Dau ◽  
Pascal Retailleau ◽  
Bogdan I. Iorga ◽  
...  
Keyword(s):  
Michael Addition ◽  
Diels Alder ◽  
Addition Reactions ◽  
Cross Metathesis

ChemInform Abstract: From Enantiopure Hydroxyaldehydes to Complex Heterocyclic Scaffolds: Development of Domino Petasis/Diels-Alder and Cross-Metathesis/Michael Addition Reactions.

ChemInform ◽  
2015 ◽  
Vol 46 (11) ◽  
pp. no-no
Author(s):  
Alexandre Cannillo ◽  
Stephanie Norsikian ◽  
Marie-Elise Tran Huu Dau ◽  
Pascal Retailleau ◽  
Bogdan I. Iorga ◽  
...  
Keyword(s):  
Michael Addition ◽  
Diels Alder ◽  
Addition Reactions ◽  
Cross Metathesis

scholarly journals Enantioselective CuII-Catalyzed Diels-Alder and Michael Addition Reactions in Water Using Bio-Inspired Triazacyclophane-Based Ligands

2011 ◽  
Vol 2011 (9) ◽  
pp. 1714-1720 ◽  
Author(s):  
H. Bauke Albada ◽  
Fiora Rosati ◽  
David Coquière ◽  
Gerard Roelfes ◽  
Rob M. J. Liskamp
Keyword(s):  
Michael Addition ◽  
Diels Alder ◽  
Addition Reactions

Reversible Diels–Alder and Michael Addition Reactions Enable the Facile Postsynthetic Modification of Metal–Organic Frameworks

2021 ◽  
Vol 60 (7) ◽  
pp. 4397-4409
Author(s):  
Sana Nayab ◽  
Vanessa Trouillet ◽  
Hartmut Gliemann ◽  
Peter G. Weidler ◽  
Iqra Azeem ◽  
...  
Keyword(s):  
Michael Addition ◽  
Metal Organic Frameworks ◽  
Diels Alder ◽  
Addition Reactions ◽  
Postsynthetic Modification ◽  
Metal Organic

Struktur und Reaktivität von isoanellierten heterocyclischen Systemen mit 4nπ- und (4n+2)π-Elektronen, XVII [1] Diels-Aider- und Michael-Additionsreaktionen von 3-Alkoxy-2,4-dihydropyrrolo[3,4-b]indolen mit Ethindicarbonsäuredialkylestern / Structure and Reactivity of Isoannelated Heterocyclic Systems with 4nπ- and (4n+2)π-Electrons, XVII [1] Diels-Alder and Michael Addition Reactions of 3-Alkoxy-2,4-dihydropyrrolo[3,4-b]indoles with Dialkyl Acetylenedicarboxylates

1988 ◽  
Vol 43 (12) ◽  
pp. 1656-1661 ◽  
Author(s):  
Gerald Dyker ◽  
Richard P. Kreher
Keyword(s):  
Michael Addition ◽  
Isotopic Labeling ◽  
Alder Reaction ◽  
Diels Alder ◽  
Addition Reactions ◽  
Current Interest ◽  
Polar Solvents ◽  
Dialkyl Acetylenedicarboxylates ◽  
Diels Alder Reaction

Abstract The reactions of 2-rm-butyl-3-methoxy-4-methyl-2,4-dihydropyrrolo[3,4-b]indole (3) with dialkyl acetylenedicarboxylates are decisively influenced by the solvent. In the presence of alcohols as protic and polar solvents Michael addition is prefered, while in aprotic and less polar solvents like ether the Diels-Alder reaction is favoured. Based on stereospecific hydrolysis and isotopic labeling dipolar intermediates are discussed. The results are of current interest for mechanistic and theoretical reasons

Studies on new hybrid materials prepared by both Diels–Alder and Michael addition reactions

2012 ◽  
Vol 111 (2) ◽  
pp. 1561-1570 ◽  
Author(s):  
Cristian-Dragos Varganici ◽  
Oana Ursache ◽  
Constantin Gaina ◽  
Viorica Gaina ◽  
Bogdan C. Simionescu
Keyword(s):  
Hybrid Materials ◽  
Michael Addition ◽  
Diels Alder ◽  
Addition Reactions
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