Enantioselective synthesis of the bisabolane sesquiterpene (+)-1-hydroxy-1,3,5-bisabolatrien-10-one and revision of its absolute configuration

Natural Product Communications

Volumn 7, Issue 4, 2012, Pages 455-458

  Serra, Stefano ^a  

^a CNR   (Italy)

Author keywords

Bisabolane sesquiterpenes; Enantioselective synthesis; Juniperus chinensis; Juniperus formosana

Indexed keywords

1 HYDROXY 1,3,5 BISABOLATRIEN 10 ONE; 3 (2 METHOXY 4 METHYLPHENYL)BUTANOL; BUTANOL; JUNIPERUS FORMOSANA EXTRACT; PLANT EXTRACT; SESQUITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOCATALYSIS; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; JUNIPERUS; JUNIPERUS CHINENSIS; JUNIPERUS FORMOSANA; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLANT LEAF; PROTON NUCLEAR MAGNETIC RESONANCE; RACEMIZATION; THIN LAYER CHROMATOGRAPHY;

JUNIPERUS CHINENSIS; JUNIPERUS FORMOSANA;

EID: 84860748468     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1200700409     Document Type: Article

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