Structurally selective electrophilic cyclization of α,ω- hydroxygeraniol derivatives by mercury(II) trifluoroacetate

Synthesis

Volumn , Issue 4, 2008, Pages 0622-0626

  Ungur, Nicon ^a,b   Garcia, Elena Zaballos ^a   Gil, Salvador ^a   Arques, José Sepulveda ^a  

^a UNIVERSITY OF VALENCIA   (Spain)

^b INSTITUTE OF CHEMISTRY   (Moldova)

Author keywords

Cyclizations; Esters; Heterocycles; Stereoselective synthesis; Terpenoids

Indexed keywords

ELECTROPHILIC CYCLIZATION; STEREOSELECTIVE SYNTHESIS;

CYCLIZATION; MERCURY (METAL); ORGANIC CARBON; SYNTHESIS (CHEMICAL);

DERIVATIVES;

ALPHA,OMEGA HYDROXYGERANIOL DERIVATIVE; GERANIOL; MERCURY DERIVATIVE; TRIFLUOROACETATE MERCURY; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CYCLIZATION; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS;

EID: 39749160412     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1032137     Document Type: Article

References (24)