Retro aza Diels-Alder reactions: acid catalyzed heterocycloreversion of 2-azanorbornenes in water at ambient temperature

Paul A. Grieco; David T. Parker; Michael Cornwell; Robert Ruckle

doi:10.1021/ja00253a053

Retro aza Diels-Alder reactions: acid catalyzed heterocycloreversion of 2-azanorbornenes in water at ambient temperature

Journal of the American Chemical Society ◽

10.1021/ja00253a053 ◽

1987 ◽

Vol 109 (19) ◽

pp. 5859-5861 ◽

Cited By ~ 48

Author(s):

Paul A. Grieco ◽

David T. Parker ◽

Michael Cornwell ◽

Robert Ruckle

Keyword(s):

Ambient Temperature ◽

Diels Alder ◽

Acid Catalyzed

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Green and Convenient One-Pot Access to Polyfunctionalized Piperidine Scaffolds via Glutamic Acid Catalyzed Knoevenagel- Intramolecular [4+2] aza-Diels-Alder Imin-Based Multi-Component Reaction Under Ambient Temperature

Polycyclic Aromatic Compounds ◽

10.1080/10406638.2018.1472111 ◽

2018 ◽

Vol 40 (3) ◽

pp. 681-692 ◽

Cited By ~ 4

Author(s):

Farzaneh Mohamadpour

Keyword(s):

Glutamic Acid ◽

Ambient Temperature ◽

Diels Alder ◽

One Pot ◽

Acid Catalyzed

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Synthesis of Medium-Sized Carbocycles via a Bidentate Lewis Acid-Catalyzed Inverse Electron-Demand Diels–Alder Reaction Followed by Photoinduced Ring-Opening

Organic Letters ◽

10.1021/acs.orglett.1c00249 ◽

2021 ◽

Author(s):

Julia Ruhl ◽

Sebastian Ahles ◽

Marcel A. Strauss ◽

Christopher M. Leonhardt ◽

Hermann A. Wegner

Keyword(s):

Lewis Acid ◽

Ring Opening ◽

Alder Reaction ◽

Diels Alder ◽

Inverse Electron Demand ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Electron Demand

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A computational investigation of the selectivity and mechanism of the Lewis acid catalyzed oxa‐Diels–Alder cycloaddition of substituted diene with benzaldehyde

Journal of Computational Chemistry ◽

10.1002/jcc.26547 ◽

2021 ◽

Author(s):

Abdelmalek Khorief Nacereddine ◽

Lynda Merzoud ◽

Christophe Morell ◽

Henry Chermette

Keyword(s):

Lewis Acid ◽

Diels Alder ◽

Computational Investigation ◽

Acid Catalyzed

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Heteropoly acid-catalyzed three-component aza-Diels–Alder reaction in a continuous micro-flow system

RSC Advances ◽

10.1039/c5ra08264a ◽

2015 ◽

Vol 5 (72) ◽

pp. 58798-58803 ◽

Cited By ~ 10

Author(s):

Wei He ◽

Zheng Fang ◽

Zhao Yang ◽

Dong Ji ◽

Kai Guo

Keyword(s):

Water Absorption ◽

Heteropoly Acid ◽

Phosphotungstic Acid ◽

Flow System ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

System P ◽

Micro Flow ◽

Acid Catalyzed

The first direct aza-Diels–Alder reaction catalyzed using phosphotungstic acid combined with a water absorption device in a micro-flow system was reported.

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

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)00201-9 ◽

2000 ◽

Vol 11 (12) ◽

pp. 2509-2523 ◽

Cited By ~ 3

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

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ChemInform Abstract: Lewis Acid Catalyzed Hetero Diels-Alder Cycloadditions of 3-Alkyl, 3-Phenyl and 3-Carboxylated 2H-Azirines.

ChemInform ◽

10.1002/chin.200211143 ◽

2010 ◽

Vol 33 (11) ◽

pp. no-no

Author(s):

Colin A. Ray ◽

Erik Risberg ◽

Peter Somfai

Keyword(s):

Lewis Acid ◽

Diels Alder ◽

Acid Catalyzed

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ChemInform Abstract: DIASTEROFACE-DISCRIMINATIVE METAL COORDINATION IN ASYMMETRIC SYNTHESIS: D-PANTOLACTONE AS PRACTICAL CHIRAL AUXILIARY FOR LEWIS ACID CATALYZED DIELS-ALDER REACTIONS

Chemischer Informationsdienst ◽

10.1002/chin.198541072 ◽

1985 ◽

Vol 16 (41) ◽

Author(s):

T. POLL ◽

A. SOBCZAK ◽

H. HARTMANN ◽

G. HELMCHEN

Keyword(s):

Asymmetric Synthesis ◽

Lewis Acid ◽

Diels Alder ◽

Chiral Auxiliary ◽

Metal Coordination ◽

Acid Catalyzed

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Complete regio- and stereospecificity in the Lewis acid catalyzed Diels-Alder reactions of (Z)-2-methoxy-1-(phenylthio)-1,3-butadienes. Conversion of the CS configuration of an adduct to the CC configuration at the allylic position by a [2,3] sigmatropic rearrangement

The Journal of Organic Chemistry ◽

10.1021/jo00141a047 ◽

1982 ◽

Vol 47 (20) ◽

pp. 4005-4008 ◽

Cited By ~ 35

Author(s):

Theodore Cohen ◽

Zenyk Kosarych

Keyword(s):

Lewis Acid ◽

Sigmatropic Rearrangement ◽

Diels Alder ◽

Acid Catalyzed

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Frontispiece: The Brønsted Acid-Catalyzed, Enantioselective Aza-Diels-Alder Reaction for the Direct Synthesis of Chiral Piperidones

Chemistry - A European Journal ◽

10.1002/chem.201780362 ◽

2017 ◽

Vol 23 (3) ◽

Author(s):

Claudia Weilbeer ◽

Marcel Sickert ◽

Sergei Naumov ◽

Christoph Schneider

Keyword(s):

Direct Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Bronsted Acid ◽

Brønsted Acid ◽

Diels Alder Reaction ◽

Brönsted Acid ◽

Acid Catalyzed

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ChemInform Abstract: Studies on Novel Synthetic Methodologies. Part 176. Tungstophosphoric Acid-Catalyzed Imino-Diels-Alder Reaction: An Efficient One-Pot Synthesis of Pyrano- and Furanoquinoline Derivatives.

ChemInform ◽

10.1002/chin.201014155 ◽

2010 ◽

Vol 41 (14) ◽

Author(s):

Biswanath Das ◽

P. Balasubramanyam ◽

Maddeboina Krishnaiah ◽

Boyapati Veeranjaneyulu

Keyword(s):

Alder Reaction ◽

Diels Alder ◽

Tungstophosphoric Acid ◽

One Pot ◽

One Pot Synthesis ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Synthetic Methodologies

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