Synthesis of strained tricyclic β-lactams by intramolecular [2+2] cycloaddition reactions of 2-azetidinone-tethered enallenols: Control of regioselectivity by selective alkene substitution

Chemistry - A European Journal

Volumn 12, Issue 5, 2006, Pages 1539-1546

  Alcaide, Benito ^a   Almendros, Pedro ^b   Aragoncillo, Cristina ^a   Redondo, María C ^a   Rosario Torres, M ^a  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b INSTITUTO DE QUÍMICA ORGÁNICA GENERAL   (Spain)

Author keywords

Allenes; Cyclization; Cycloaddition; Lactams; Radicals

Indexed keywords

ADDITION REACTIONS; INDIUM; OLEFINS; PYROLYSIS; SUBSTITUTION REACTIONS;

ALLENES; CYCLIZATION; CYCLOADDITION; LACTAMS; RADICALS;

NITROGEN COMPOUNDS;

2 AZETIDINONE; 2-AZETIDINONE; ALKENE; ALLENOLIC ACID; AZETIDINE DERIVATIVE; BETA LACTAM; CYCLOBUTANE DERIVATIVE; NAPHTHALENE DERIVATIVE;

ARTICLE; CHEMISTRY; SYNTHESIS;

ALKENES; AZETIDINES; BETA-LACTAMS; CYCLOBUTANES; NAPHTHALENES;

EID: 32044451039     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200500807     Document Type: Article

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