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- W1595146534 abstract "Abstract Stereochemistry of oxypalladation for e-hydroxy chiral allylic alcohol is described. anti- and syn-face selective syn-oxypalladation to a chiral allyl alcohol takes place and provides enantiomerically opposite 2-(Z)-alkenyl and 2-(E)-alkenyl substituted oxacyclic rings in a ratio of 2:3." @default.
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- W1595146534 date "2015-07-01" @default.
- W1595146534 modified "2023-10-09" @default.
- W1595146534 title "ChemInform Abstract: Hydroxy Group Directed Stereochemistry in Oxypalladation of Chiral Allylic Alcohol." @default.
- W1595146534 cites W2949403133 @default.
- W1595146534 doi "https://doi.org/10.1002/chin.201530145" @default.
- W1595146534 hasPublicationYear "2015" @default.
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