A new one-pot synthetic method for selenium-containing medium-sized α,β-unsaturated cyclic ketones

Synthesis

Volumn , Issue 20, 2008, Pages 3229-3236

  Sashida, Haruki ^a   Nakayama, Akemi ^a   Kaname, Mamoru ^a  

^a HOKURIKU UNIVERSITY   (Japan)

Author keywords

Ethynyllithium; Ring expansion; Selenium; Selenoketone; Selenolactone

Indexed keywords

ORGANIC COMPOUNDS; SELENIUM;

CARBON RINGS; CYCLIC KETONES; ETHYNYLLITHIUM; ONE POTS; RING EXPANSION; SELENOKETONE; SELENOLACTONE; SYNTHETIC METHODS;

KETONES;

2 (4 METHOXYPHENYL) 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 (4 METHOXYPHENYL) 6,7 DIHYDRO 5H SELENEPIN 4 ONE; 2 (4 TRIFLUOROMETHYLPHENYL) 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 4 TOLYL 5,6,7,8 TETAHYDROSELENOCIN 4 ONE; 2 4 TOLYL 6,7 DIHYDRO 5H SELENEPIN 4 ONE; 2 BUTYL 5 METHYL 5,6,7,8 TETRAGHYDROSELENOCIN 4 ONE; 2 BUTYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 BUTYL 8 METHYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 CYCLOHEX 1 ENYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 PHENYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 PHENYL 6,7 DIHYDRO 5H SELENEPIN 4 ONE; 2 TERT BUTYL 5 METHYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 TERT BUTYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 TERT BUTYL 6,7 DIHYDRO 5H SELENEPIN 4 ONE; 2 TERT BUTYL 8 METHYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 2 TRIMETHYLSILYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 3 METHYLDIHYDROSELENOPHEN 2 ONE; 3 METHYLTETRAHYDROSELENOPYRAN 2 ONE; 5 METHYL 2 PHENYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 5 METHYL 2 PHENYL 6,7 DIHYDRO 5H SELENEPIN 4 ONE; 5 METHYL 2 TRIMETHYLSILYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 6 METHYLTETRAHYDROSELENOPYRAN 2 ONE; 8 METHYL 2 PHENYL 5,6,7,8 TETRAHYDROSELENOCIN 4 ONE; 8 METHYL 2 TRIMETHYLSILYL 5,6,7,8 TETAHYDROSELENOCIN 4 ONE; DIHYDROSELENOPHEN 2 ONE; LACTONE DERIVATIVE; SELENEPAN 2 ONE; SELENIUM; TETRAHYDROSELENOPYRAN 2 ONE; TETRAHYDROTELLUROPYRAN 2 ONE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 55349135917     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1083153     Document Type: Article

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