ChemInform Abstract: Stereoselective Synthesis of cis-Decalins via Diels-Alder and Double Michael Addition of Substituted Nazarov Reagents.

ChemInform ◽  
2010 ◽  
Vol 24 (5) ◽  
pp. no-no
Author(s):  
J.-F. LAVALLEE ◽  
C. SPINO ◽  
R. RUEL ◽  
K. T. HOGAN ◽  
P. DESLONGCHAMPS
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Diels Alder

Stereoselective synthesis of cis-decalins via Diels–Alder and double Michael addition of substituted Nazarov reagents

1992 ◽  
Vol 70 (5) ◽  
pp. 1406-1426 ◽  
Author(s):  
Jean-François Lavallée ◽  
Claude Spino ◽  
Réjean Ruel ◽  
Keith T. Hogan ◽  
Pierre Deslongchamps
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Diels Alder

The base-catalyzed cycloaddition and double Michael cyclization of substituted Nazarov reagents and of 1-phenylsulfinyl analogs, with 2-carbomethoxy-2-cyclohexen-1-one 1 yielding cis-decalins is reported. The reaction is highly stereoselective affording cis,cis- or cis, trans-decalins. Mechanistic aspects are briefly discussed.

A Combined Vinylogous Mannich/Diels-Alder Approach for the Stereoselective Synthesis of Highly Functionalized Hexahydroindoles

2011 ◽  
Vol 2011 (32) ◽  
pp. 6558-6566 ◽  
Author(s):  
Bettina M. Ruff ◽  
Sabilla Zhong ◽  
Martin Nieger ◽  
Marcel Sickert ◽  
Christoph Schneider ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Diels Alder

Uncatalyzed diastereoselective synthesis of alkyliminofurochromone-derived benzylmalononitriles via a three-component cascade reaction: competition between Diels–Alder cycloaddition and Michael addition

2021 ◽  
Author(s):  
Mohammad Bagher Teimouri ◽  
Zahra Mokhtare ◽  
Hamid Reza Khavasi
Keyword(s):  
Michael Addition ◽  
Heterocyclic Ring ◽  
Cascade Reaction ◽  
Diels Alder ◽  
Chemical Bonds ◽  
Diastereoselective Synthesis ◽  
Atom Economy ◽  
One Pot

Three new chemical bonds and three stereogenic centres and one heterocyclic ring were assembled stereoselectively in a convenient high atom-economy one-pot operation.

Domino Knoevenagel–hetero-Diels–Alder reactions: a stereoselective synthesis of sugar-annulated furo[3,2-b] pyrano[4,3-d]pyran derivatives

2010 ◽  
Vol 51 (17) ◽  
pp. 2305-2308 ◽  
Author(s):  
J.S. Yadav ◽  
B.V. Subba Reddy ◽  
A.V. Hara Gopal ◽  
R. Nageshwar Rao ◽  
R. Somaiah ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Diels Alder

ChemInform Abstract: 2-Azanorbornane - A Versatile Chiral aza-Diels-Alder Cycloadduct: Preparation, Applications in Stereoselective Synthesis and Biological Activity

ChemInform ◽  
2015 ◽  
Vol 46 (31) ◽  
pp. no-no
Author(s):  
Elzbieta Wojaczynska ◽  
Jacek Wojaczynski ◽  
Karolina Kleniewska ◽  
Mateusz Dorsz ◽  
Tomasz K. Olszewski
Keyword(s):  
Biological Activity ◽  
Stereoselective Synthesis ◽  
Diels Alder

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
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