Strategies for spiroketal synthesis based on transition-metal catalysis

Synthesis (Germany)

Volumn 44, Issue 24, 2012, Pages 3699-3721

  Palmes, Jean A ^a   Aponick, Aaron ^a  

^a UNIVERSITY OF FLORIDA   (United States)

Author keywords

acetals; catalysis; natural products; spiroketals; transition metal catalysis

Indexed keywords

[2+2+2] CYCLOADDITION; ACETALS; ALLYLIC ALCOHOL; ARYL IODIDES; CONFORMATIONAL ASPECTS; CROSS COUPLING REACTIONS; DIENONES; DIFFERENT SUBSTRATES; EPOXY ALKYNES; HETERO-DIELS-ALDER REACTIONS; INTRAMOLECULAR REACTIONS; NATURAL PRODUCT SYNTHESIS; NATURAL PRODUCTS; PAUSON-KHAND REACTIONS; PROPARGYL; RING CLOSING METATHESIS; SPIROKETALS; SYNTHONS; TANDEM CYCLIZATION; VINYL ETHERS;

ACETYLENE; CARBOHYDRATES; CATALYSIS; CYCLOADDITION; ETHERS; SYNTHESIS (CHEMICAL); TRANSITION METALS;

CYCLIZATION;

ALKYNE DERIVATIVE; ALKYNEDIOL; ARYL IODIDE; BETA BROMOKETAL; DIENONE DERIVATIVE; EPOXY ALKYNE DERIVATIVE; HEMIACETAL; KETODIOL; MONOPROPARGYIC TRIOL; NATURAL PRODUCT; OKADAIC ACID; SPIROKETAL; SPONGISTATIN 1; SPONGISTATIN 2; TAUTOMYCIN; UNCLASSIFIED DRUG;

CARBONYLATION; CATALYSIS; CHEMICAL STRUCTURE; CONFORMATIONAL TRANSITION; CROSS COUPLING REACTION; CYCLIZATION; CYCLOADDITION; DIELS ALDER REACTION; ISOMERIZATION; PHARMACOPHORE; PROTEIN MOTIF; REVIEW; RING CLOSING METATHESIS; RING OPENING METATHESIS POLYMERIZATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 84870891522     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1317489     Document Type: Review

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