Lewis Acid Catalyzed Procedure for Selective Conversion of the Carbocyclic Diels-Alder Adducts of Danishefsky's Diene to 2-Cyclohexenones and Its Extension to Their One-Pot Syntheses

Synlett ◽

10.1055/s-2000-7940 ◽

2000 ◽

Vol 2000 (11) ◽

pp. 1549-1552 ◽

Keyword(s):

Diels Alder ◽

One Pot ◽

Selective Conversion ◽

Acid Catalyzed ◽

Danishefsky's Diene

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ChemInform Abstract: Lewis Acid Catalyzed Procedure for Selective Conversion of the Carbocyclic Diels-Alder Adducts of Danishefsky′s Diene to 2-Cyclohexenones and Its Extension to Their One-Pot Syntheses.

10.1002/chin.200108108 ◽

2001 ◽

Vol 32 (8) ◽

pp. no-no

Author(s):

Tsutomu Inokuchi ◽

Masamitsu Okano ◽

Tomoko Miyamoto ◽

Hariyani Bte Madon ◽

Masaki Takagi

Keyword(s):

Diels Alder ◽

One Pot ◽

Selective Conversion ◽

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Lewis acid-catalyzed Diels-Alder reaction of 2-cyclopentenones with Danishefsky’s diene: double bond isomerization of tetrahydro-1H-indene-1,5(7aH)-diones, and attempts on an asymmetric catalysis

ARKIVOC ◽

10.3998/ark.5550190.0013.302 ◽

2011 ◽

Vol 2012 (3) ◽

pp. 5-19

Author(s):

Michael Krebs ◽

Sabine Laschat

Keyword(s):

Double Bond ◽

Asymmetric Catalysis ◽

Alder Reaction ◽

Diels Alder ◽

Double Bond Isomerization ◽

Diels Alder Reaction ◽

Acid Catalyzed ◽

Danishefsky's Diene

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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):

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):

Diels Alder ◽

Computational Investigation ◽

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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 ◽

Author(s):

Renée Paugam ◽

Emmanuelle Valenciennes ◽

Linda Le Coz-Bardol ◽

Jean-Christophe Garde ◽

Lya Wartski ◽

...

Keyword(s):

Asymmetric Synthesis ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

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

10.1002/chin.200211143 ◽

2010 ◽

Vol 33 (11) ◽

pp. no-no

Author(s):

Colin A. Ray ◽

Erik Risberg ◽

Peter Somfai

Keyword(s):

Diels Alder ◽

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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 ◽

Diels Alder ◽

Chiral Auxiliary ◽

Metal Coordination ◽

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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 ◽

Author(s):

Theodore Cohen ◽

Zenyk Kosarych

Keyword(s):

Sigmatropic Rearrangement ◽

Diels Alder ◽

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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.

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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A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction

Chemical Communications ◽

10.1039/c4cc01791a ◽

2014 ◽

Vol 50 (82) ◽

pp. 12270-12272 ◽

Author(s):

V. P. Alex Raja ◽

Giammarco Tenti ◽

Subbu Perumal ◽

J. Carlos Menéndez

Keyword(s):

Heavy Metal ◽

Multicomponent Reaction ◽

One Pot ◽

One Pot Synthesis ◽

Pyridines and fused pyridines are accessible by a combination of a Lewis acid-catalyzed multicomponent reaction and aromatization involving loss of a 2-furylmethyl chain.

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