Recent synthetic strategies to access seven-membered carbocycles in natural product synthesis

Synthesis (Germany)

Volumn 45, Issue 7, 2013, Pages 845-873

  Nguyen, Thanh Vinh ^a   Hartmann, Jan Marc ^a   Enders, Dieter ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

medium sized carbocycles; natural products; seven membered carbocycles; synthetic strategy; total synthesis

Indexed keywords

CARBOCYCLES; ISOMERIZATION REACTION; NATURAL PRODUCT SYNTHESIS; NATURAL PRODUCTS; RING CLOSING METATHESIS; RING-EXPANSION REACTION; SYNTHETIC STRATEGIES; TOTAL SYNTHESIS;

CYCLIZATION; CYCLOADDITION;

ISOMERIZATION;

13 OXYINGENOL DERIVATIVE; ALLOCOLCHICINE; APLYVIOLENE; CALYSTEGINE A3; CHINENSIOLIDE B; COLCHICINE; CORTISTATIN A; CORTISTATIN K; CORTISTATIN L; CYRNEINE A; DRAGMACIDIN E; ECHINOPINES A; ECHINOPINES B; ENGLERIN A; ENGLERIN B; FRONDOSIN B; GUANACASTEPENE A; GUANACASTEPENE N; GUANACASTEPENE O; HEPTEMERONE B; HEPTEMERONE G; INGENOL; LIPHAGAL; NATURAL PRODUCT; OMPHADIOL; ORIENTALOL F; PAREITROPONE; UNCLASSIFIED DRUG; WELWITINDOLINONE B; XANTHATIN;

CHEMICAL ANALYSIS; CYCLIZATION; CYCLOADDITION; DIELS ALDER REACTION; FRAGMENTATION REACTION; ISOMERIZATION; REVIEW; RING CLOSING METATHESIS; SYNTHESIS;

EID: 84875232965     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0032-1318152     Document Type: Review

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