Straightforward Asymmetric Entry to Highly Functionalized 3-Substituted 3-Hydroxy-p-lactams via Baylis-Hillman or Bromoallylation Reactions

Journal of Organic Chemistry

Volumn 69, Issue 3, 2004, Pages 826-831

  Alcaide, Benito ^a   Almendros, Pedro ^b   Aragoncillo, Cristina ^a   Rodríguez Acebes, Raquel ^a  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b INSTITUTO DE QUÍMICA ORGÁNICA GENERAL   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL ANALYSIS; ISOMERS; SUBSTITUTION REACTIONS;

EPIMERIZATIONS;

ORGANIC COMPOUNDS;

2,3 AZETIDINEDIONE DERIVATIVE; 2,3 DIBROMOPROPENE; ALCOHOL; ALPHA KETO LACTAM; BETA LACTAM DERIVATIVE; CYCLOPENTENONE; INDIUM; METAL; PROPYLENE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; BAYLIS HILLMAN REACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; ENANTIOMER; EPIMERIZATION; SYNTHESIS;

ALLYL COMPOUNDS; ANTI-BACTERIAL AGENTS; AZETIDINES; BETA-LACTAMS; HYDROCARBONS, BROMINATED; STEREOISOMERISM;

EID: 0842328942     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo035472l     Document Type: Article

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