Pd(0)/lnl-mediated allylic additions to 4-acetoxy-2-azetidinone: New route to highly functionalized carbocyclic scaffolds

Organic Letters

Volumn 11, Issue 6, 2009, Pages 1293-1295

  Cesario, Cara ^a   Miller, Marvin J ^a  

^a UNIVERSITY OF NOTRE DAME   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 ACETOXY 2 AZETIDINONE; 4-ACETOXY-2-AZETIDINONE; AZETIDINE DERIVATIVE; CYCLOPENTANE DERIVATIVE; HYDROXAMIC ACID; INDIUM; PALLADIUM;

ARTICLE; CATALYSIS; CHEMISTRY; CONFORMATION; CYCLIZATION; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

AZETIDINES; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; CYCLOPENTANES; HYDROXAMIC ACIDS; INDIUM; MOLECULAR CONFORMATION; PALLADIUM; STEREOISOMERISM;

EID: 64049097700     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol9000685     Document Type: Article

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19. Hydroxamic acid 11 was purified on iron-free silica gel; refer to the Supporting Information for preparation of iron-free silica gel.
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