The IntramolecularMichael Reaction - Wikidata - awgldk - TriplyDB

The IntramolecularMichael Reaction

The IntramolecularMichael Reaction

http://www.wikidata.org/entity/Q56455937

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Total synthesis of the Galbulimima alkaloid (-)-GB17 Highly Functionalized Cyclopentane Derivatives by Tandem Michael Addition/Radical Cyclization/Oxygenation Reactions.

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The IntramolecularMichael Reaction

http://www.wikidata.org/entity/Q56455937

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wetenschappelijk artikel

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наукова стаття, опублікована у квітні 1995

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name

The IntramolecularMichael Reaction

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The IntramolecularMichael Reaction

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type

label

The IntramolecularMichael Reaction

@en

The IntramolecularMichael Reaction

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prefLabel

The IntramolecularMichael Reaction

@en

The IntramolecularMichael Reaction

@nl

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0471264180.OR047.02

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The IntramolecularMichael Reaction

@en

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Jim I. Mcloughlin

http://www.w3.org/2001/XMLSchema#string

Mohammad R. Masjedizadeh

http://www.w3.org/2001/XMLSchema#string

Olof Wallquist

http://www.w3.org/2001/XMLSchema#string

R. Daniel Little

http://www.w3.org/2001/XMLSchema#string

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Rules for ring closure

Rules for ring closure: ring formation by conjugate addition of oxygen nucleophiles

Azabicycloalkanes as analgetics. VI. 5-Phenyl-2-azabicyclo[3,2,1]octanes.

Stereopopulation control. 3. Facilitation of intramolecular conjugate addition of the carboxyl group.

Synthesis and biological properties of 5-aryl-4H-1,2,4-thiadiazine 1,1-dioxides.

Syntheses of 3,4-dihydro-2H-1,4-benzoxazine-2-acetates and related compounds.

Intramolecular michael addition reaction to chiral vinylic sulfoxides. An enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecane

Total Synthesis of Longifolene

Synthese des Colchicins

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315-552

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scholarly article

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10.1002/0471264180.OR047.02

http://www.w3.org/2001/XMLSchema#string

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1995-04-03T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime