161040-07-9Relevant articles and documents
δ-Unsaturated γ-amino acids: Enantiodivergent synthesis and cell imaging studies
Kand, Dnyaneshwar,Chauhan, Dinesh Pratapsinh,Lahiri, Mayurika,Talukdar, Pinaki
supporting information, p. 3591 - 3593 (2013/05/09)
Synthesis of both enantiomers of δ-unsaturated γ-amino acids via the enantiodivergent [3,3]-sigmatropic rearrangement strategy is reported. Excellent enantiomeric excess > 94% are observed in the strategy. Cell permeability of a fluorescent amino acid derivative is evaluated by live-cell imaging.
Remote allylic silyloxy groups as stereocontrol elements in intramolecular oxymercurations of γ-hydroxyalkenes
Bratt, Katharina,Garavelas, Agatha,Perlmutter, Patrick,Westman, Gunnar
, p. 2109 - 2117 (2007/10/03)
The diastereoselectivity in intramolecular oxymercurations of γ-hydroxyalkenes bearing a remote allylic oxy substituent has been investigated. It was found that the best selectivity was obtained by employing a combination of (Z)-alkene geometry and a tert-butyldiphenylsilyl protecting group attached to the remote allylic oxygen as in 4a-g. Cyclization, using mercuric acetate in dichloromethane, of all the (Z)-alkenols gave the syn diastereomer, 5a-g, as the major product. For example, cyclization of 4b gave syn diastereomer 5b and anti diastereomer 6b in a ratio of 7:1. It was found that this ratio could be improved by replacing dichloromethane with acetonitrile. Under these conditions the ratio of 5b to 6b increased to 19:1. Cyclization of (E)-alkene 9 gave very poor diastereoselection. These syn-selective intramolecular oxymercurations were exploited in enantioselective syntheses of two diastereomers of methyl nonactate.
