Asymmetric synthesis of trans-4,5-dioxygenated cyclopentenone derivatives by organocatalyzed rearrangement of pyranones and enzymatic dynamic kinetic resolution

Tetrahedron

Volumn 67, Issue 15, 2011, Pages 2779-2787

  Nunes, João P M ^a   Veiros, Luís F ^a   Vaz, Pedro D ^b   Afonso, Carlos A M ^a,c   Caddick, Stephen ^d  

^a INSTITUTO SUPERIOR TÉCNICO   (Portugal)

^b UNIVERSITY OF LISBON   (Portugal)

^c RESEARCH INSTITUTE FOR MEDICINES IMED ULISBOA   (Portugal)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Dynamic kinetic resolution; Lipase catalyzed acylation; Organocatalysis; Pyranone rearrangement; trans Dioxygenated cyclopentenone

Indexed keywords

AMINE; CYCLOPENTENONE DERIVATIVE; LACTONE DERIVATIVE; SOLVENT;

ARTICLE; ASYMMETRIC SYNTHESIS; CATALYSIS; CYCLIZATION; ENERGY; ENZYME KINETICS; PRIORITY JOURNAL; REACTION ANALYSIS; REACTION OPTIMIZATION; RING OPENING; SOLVENT EFFECT; TEMPERATURE SENSITIVITY; TRANS ISOMER;

EID: 79952902085     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.02.018     Document Type: Article

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