Periselective, Lewis acid-induced intramolecular Diels–Alder reaction of conjugated carbodiimides: efficient synthesis of nitrogen heterocycles, indolo[2,3-b]quinolines and pyrido[2,3-b]indole

1993 ◽  
pp. 1802-1803 ◽  
Author(s):  
Takao Saito ◽  
Hiromasa Ohmori ◽  
Takahiro Ohkubo ◽  
Shinichi Motoki
Keyword(s):  
Lewis Acid ◽  
Nitrogen Heterocycles ◽  
Alder Reaction ◽  
Diels Alder ◽  
Efficient Synthesis ◽  
Diels Alder Reaction

scholarly journals An efficient synthesis of chiral isoquinuclidines by Diels–Alder reaction using Lewis acid catalyst

Tetrahedron ◽  
2010 ◽  
Vol 66 (38) ◽  
pp. 7618-7624 ◽  
Author(s):  
Masafumi Hirama ◽  
Yuji Kato ◽  
Chigusa Seki ◽  
Hiroto Nakano ◽  
Mitsuhiro Takeshita ◽  
...  
Keyword(s):  
Lewis Acid ◽  
Acid Catalyst ◽  
Alder Reaction ◽  
Diels Alder ◽  
Efficient Synthesis ◽  
Diels Alder Reaction ◽  
Lewis Acid Catalyst

Enantioselective Syntheses of Flavonoid Diels-Alder Natural Products: A Review

2018 ◽  
Vol 15 (2) ◽  
pp. 221-229 ◽  
Author(s):  
Shah Bakhtiar Nasir ◽  
Noorsaadah Abd Rahman ◽  
Chin Fei Chee
Keyword(s):  
Natural Products ◽  
Organic Synthesis ◽  
Lewis Acid ◽  
Alder Reaction ◽  
Diels Alder ◽  
Enantioselective Synthesis ◽  
Chiral Ligand ◽  
Asymmetric Syntheses ◽  
Diels Alder Reaction ◽  
Enantioselective Syntheses

Background: The Diels-Alder reaction has been widely utilised in the syntheses of biologically important natural products over the years and continues to greatly impact modern synthetic methodology. Recent discovery of chiral organocatalysts, auxiliaries and ligands in organic synthesis has paved the way for their application in Diels-Alder chemistry with the goal to improve efficiency as well as stereochemistry. Objective: The review focuses on asymmetric syntheses of flavonoid Diels-Alder natural products that utilize chiral ligand-Lewis acid complexes through various illustrative examples. Conclusion: It is clear from the review that a significant amount of research has been done investigating various types of catalysts and chiral ligand-Lewis acid complexes for the enantioselective synthesis of flavonoid Diels-Alder natural products. The results have demonstrated improved yield and enantioselectivity. Much emphasis has been placed on the synthesis but important mechanistic work aimed at understanding the enantioselectivity has also been discussed.

Asymmetric synthesis of N-phenylethyl-2-phenyldecahydroquinolin-4-ones via Lewis acid catalyzed imino-Diels–Alder reaction

2000 ◽  
Vol 11 (12) ◽  
pp. 2509-2523 ◽  
Author(s):  
Renée Paugam ◽  
Emmanuelle Valenciennes ◽  
Linda Le Coz-Bardol ◽  
Jean-Christophe Garde ◽  
Lya Wartski ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Lewis Acid ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Acid Catalyzed

Asymmetric synthesis of isoquinuclidines by Diels–Alder reaction of 1,2-dihydropyridine utilizing a chiral Lewis acid catalyst

Tetrahedron ◽  
2012 ◽  
Vol 68 (6) ◽  
pp. 1774-1781 ◽  
Author(s):  
Chigusa Seki ◽  
Masafumi Hirama ◽  
N.D.M. Romauli Hutabarat ◽  
Junko Takada ◽  
Chonticha Suttibut ◽  
...  
Keyword(s):  
Asymmetric Synthesis ◽  
Lewis Acid ◽  
Acid Catalyst ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Chiral Lewis Acid ◽  
Lewis Acid Catalyst

An Efficient Synthesis of New C-2 Aryl-Substituted Quinolines Based on Three-Component Imino Diels—Alder Reaction.

ChemInform ◽  
2006 ◽  
Vol 37 (24) ◽  
Author(s):  
Vladimir Kouznetsov ◽  
Arnold R. Romero Bohorquez ◽  
Luis Astudillo Saavedra ◽  
Ricardo Fierro Medina
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Efficient Synthesis ◽  
Diels Alder Reaction ◽  
Substituted Quinolines
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