An Ireland-claisen rearrangement/lactonisation cascade as a key step in studies towards the synthesis of (-)-euonyminol

Synlett

Volumn , Issue 18, 2011, Pages 2693-2696

  Webber, Matthew J ^a   Weston, Matthew ^b   Grainger, Damian M ^a,b   Lloyd, Stacy ^a   Warren, Sarah A ^a   Powell, Lyn ^c   Alanine, Alexander ^d   Stonehouse, Jeffrey P ^c   Frampton, Christopher S ^e   White, Andrew J P ^a   Spivey, Alan C ^a,b  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF SHEFFIELD   (United Kingdom)

^c ASTRAZENECA   (United Kingdom)

^d F HOFFMANN LA ROCHE LTD   (Switzerland)

^e Sigma Aldrich Group   (United Kingdom)

Author keywords

bromination; Celastraceae; euonyminol; Ireland Claisen; sesquiterpene

Indexed keywords

ALCOHOL DERIVATIVE; ALLYLIC ESTER; ALPHA BROMOLACTONE; BENZOATE ESTER; BENZOYL ESTER; BETA DIHYDROAGAROFURAN; BROMOLACTONE; EPOXIDE; ESTER DERIVATIVE; EUONYMINOL; HYPOGLAUNINE B; LACTONE DERIVATIVE; SESQUITERPENE; SILYL ESTER EPOXIDE; TRIPTONINE B; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; BROMINATION; CLAISEN REARRANGEMENT; CONTROLLED STUDY; DIASTEREOISOMER; DRUG STRUCTURE; DRUG SYNTHESIS; IRELAND CLAISEN REARRANGEMENT; LACTONIZATION; OXYGENATION; PROCESS DEVELOPMENT;

EID: 80455122612     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1289543     Document Type: Article

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