Formal [4 + 2] cycloaddition of donor-acceptor cyclobutanes and aldehydes: Stereoselective access to substituted tetrahydropyrans

Journal of the American Chemical Society

Volumn 131, Issue 40, 2009, Pages 14202-14203

  Parsons, Andrew T ^a   Johnson, Jeffrey S ^a  

^a University of North Carolina at Chapel Hill   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

[2+2+2] CYCLOADDITION; [4 + 2] CYCLOADDITION; ALIPHATIC ALDEHYDES; CHEMICAL EQUATIONS; CYCLOBUTANES; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE SYNTHESIS; DIPOLAROPHILES; DONOR-ACCEPTORS; LEWIS ACID; MALONATES; STEREO-SELECTIVE;

BUTANE; CHEMICAL REACTIONS; STEREOSELECTIVITY;

ALDEHYDES;

2 CHLOROBENZALDEHYDE; 2,2 METHYLIDENE MALONATE; 4 METHOXYSTYRENE; ALDEHYDE DERIVATIVE; ALKENE; CINNAMALDEHYDE; CYCLOBUTANE DERIVATIVE; LEWIS ACID; MALONIC ACID; NUCLEOPHILE; STYRENE; TETRAHYDROFURAN DERIVATIVE; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CYCLOADDITION; DIASTEREOISOMER; RING OPENING; STEREOCHEMISTRY; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

ALDEHYDES; ALKENES; CYCLIZATION; CYCLOBUTANES; MALONATES; PYRANS; STEREOISOMERISM;

EID: 70349910424     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja906755e     Document Type: Article

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