Novel synthetic methods for the preparation of optically active fluorine-containing building blocks on the basis of sigmatropic rearrangements

Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry

Volumn 63, Issue 1, 2005, Pages 26-39

  Konno, Tsutomu ^a  

^a KYOTO INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

1,3 allylic rearrangement; Amino acids; Difluorocarbene mediated reaction; Double rearrangements; Enzymatic resolution; Eshenmoser Claisen; Iodolactonization; Ireland Claisen; Johnson Claisen; Multifunctionalized compounds; Osmylation; 2,3 Wittig

Indexed keywords

ALKYLATION; AMINO ACIDS; ENZYME KINETICS; FLUORINE; LIGHT SENSITIVE MATERIALS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

1,3-ALLYLIC REARRANGEMENT; DIFLUOROCARBENE-MEDIATED REACTION; DOUBLE REARRANGEMENTS; ENZYMATIC RESOLUTION; ESHENMOSER-CLAISEN SHIFT; IODOLACTONIZATION; IRELAND-CLAISEN SHIFT; JOHNSON-CLAISEN SHIFT; OSMYLATION; [2,3]-WITTIG SHIFT;

ALCOHOLS;

EID: 15744372542     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.63.26     Document Type: Article

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