Enantioconvergent tactic for the synthesis of (+)-sporochnol A, the fish deterrent from the Caribbean marine alga Sporochnus bolleanus

Enantiomer

Volumn 2, Issue 3-4, 1997, Pages 297-301

  Kamikubo, Takashi ^a   Shimizu, Masahiro ^a   Ogasawara, Kunio ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Absolute configuration of (+) sporochnol A; Chiral 3 methyl 2,5 cyclohexadienone synthon; Enantioconvergent synthesis; Fish deterrent from Sporochnus bolleanus; Lipase mediated resolution; Palladium mediated elimination

Indexed keywords

NATURAL PRODUCT; PHENOL DERIVATIVE; TRIACYLGLYCEROL LIPASE;

ALGA; CHEMICAL REACTION; CHIRALITY; CONFERENCE PAPER; DRUG SYNTHESIS; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REACTION ANALYSIS;

ALGAE; SPOROCHNUS BOLLEANUS;

EID: 0030808158     PISSN: 10242430     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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