Regio- and stereoselectivity in the Lewis acid- and NaH-induced reactions of thiocamphor with (R)-2-vinyloxirane

Helvetica Chimica Acta

Volumn 89, Issue 3, 2006, Pages 456-467

  Fedorov, Alexey ^a,b,c   Fu, Changchun ^a   Heimgartner, Heinz ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b ST PETERSBURG STATE UNIVERSITY   (Russian Federation)

^c ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; HEPTANE; ISOMERS; KETONES; REACTION KINETICS; SODIUM COMPOUNDS;

ISOMERIC ENESULFANYL ALCOHOL; NAH-INDUCED REACTIONS; THIOCAMPHORS;

HYDROCARBONS;

1,2 EPOXY 3 BUTENE; 1,3 OXATHIOLANE DERIVATIVE; 1,3,5 TRIMETHYLBENZENE; 1,7,7 TRIMETHYLBICYCLO[2.2.1]HEPTANE 2 THIONE; 2 VINYLORIXANE; 4 VINYL 1,3 OXATHIOLANE DERIVATIVE; ALCOHOL; CAMPHOR; CARBONIC ACID; DITHIOCARBONATE; HEPTANE DERIVATIVE; LEWIS ACID; THIOKETONE; UNCLASSIFIED DRUG; VINYL DERIVATIVE; XANTHIC ACID DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CLAISEN REARRANGEMENT; CYCLIZATION; DIASTEREOISOMER; EPIMER; PRIORITY JOURNAL; ROOM TEMPERATURE; STEREOCHEMISTRY;

EID: 33645571370     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200690046     Document Type: Article

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