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- W1991787162 abstract "The 3,4-stereochemistry of aldol adducts can now be controlled for the first time with the new, chiral, readily accessible enolate reagent (2); i.e. the chiral aldehyde (1) can be transformed both into 3,4-anti- and into the 3,4-syn-aldol adduct, (3) and (4), as major product. (2a) forms (3a) and (4a) in the ratio of 15:1, while (2b) leads to (3b) and (4b) in the ratio of 1:10." @default.
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- W1991787162 date "1980-07-01" @default.
- W1991787162 modified "2023-09-26" @default.
- W1991787162 title "Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral Enolate" @default.
- W1991787162 doi "https://doi.org/10.1002/anie.198005571" @default.
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