Sequencing pericyclic reactions: The ester dienolate [2,3]-wittig/oxy-cope rearrangement/carbonyl ene reaction, a new access to substituted carbocycles

European Journal of Organic Chemistry

Volumn , Issue 3, 2001, Pages 483-491

  Hiersemann, Martin ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

Carbocycles; Domino reactions; Ene reactions; Ester dienolates; Pericyclic reactions; Rearrangements

Indexed keywords

CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CYCLOHEXANE DERIVATIVE; CYCLOPENTANE DERIVATIVE; ESTER DERIVATIVE; ISOPROPYL 1 HYDROXY 2 METHYL 5 METHYLENECYCLOHEXANECARBOXYLATE; ISOPROPYL 1 HYDROXY 3 METHYLENECYCLOHEXANECARBOXYLATE; ISOPROPYL 1 HYDROXY 5 METHYLENE 3 PHENYLCYCLOHEXANECARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; ENANTIOMER; STEREOCHEMISTRY;

EID: 0035144033     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200102)2001:3<483::AID-EJOC483>3.0.CO;2-F     Document Type: Article

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