Desymmetrisation of cyclic dienes. An efficient strategy for natural products synthesis

Current Organic Chemistry

Volumn 6, Issue 15, 2002, Pages 1369-1395

  Rahman, N Abd ^a   Landais, Y ^a  

^a Lab de Synthese Organi Organomet   (France)

Author keywords

[No Author keywords available]

Indexed keywords

OLEFINS; REACTION INTERMEDIATES;

BREAKINGS; CHIRAL CENTERS; CYCLIC DIENE; CYCLOHEXADIENES; DESYM-METRIZATION; DIASTEREOCONTROL; EFFICIENT STRATEGY; ENANTIOCONTROL; NATURAL PRODUCT SYNTHESIS; SYMMETRICS;

HYDROXYLATION;

1,3 CYCLOPENTADIENE DERIVATIVE; 1,4 CYCLOHEXADIENE DERIVATIVE; ALKALOID DERIVATIVE; AMINOCYCLITOL; ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; CAPNELLENE DERIVATIIVE; CARBA C DISACCHARIDE DERIVATIVE; CARBO C FURANOSIDE DERIVATIVE; CONDURAMINE E; CYCLITOL DERIVATIVE; CYCLOHEXADIENE DERIVATIVE; CYCLOPENTADIENE DERIVATIVE; DITERPENE; ELDANOLIDE; FORTAMINE; GLYCOSIDASE INHIBITOR; NATURAL PRODUCT; PALITANTIN DERIVATIVE; PEDUNCULARINE; PINNATERPENE B; PREPINNATERPENE; PSEUDO ALPHA DEXTRO GALACTOPYRANOSE; PSEUDO BETA LEVO ALTROPYRANOSE; PSEUDOSUGAR DERIVATIVE; SESQUITERPENE DERIVATIVE; SILICON DERIVATIVE; STREPTOMYCIN; UNCLASSIFIED DRUG; UNINDEXED DRUG; VERNOLEPIN DERIVATIVE;

AMINOHYDROXYLATION; ASYMMETRIC SYNTHESIS; CHEMICAL REACTION; CYCLOPROPANATION; DIASTEREOISOMER; DIHYDROXYLATION; DRUG ACTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENZYME INHIBITION; HECK REACTION; HYDROBORATION; METHODOLOGY; OXIDATION; RADICAL REACTION; RELIABILITY; REVIEW; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 0036889564     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/1385272023373347     Document Type: Review

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