| 11. | The method then is an enantioselective asymmetric synthesis reaction.
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| 12. | This method of asymmetric synthesis is economically most desirable.
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| 13. | Asymmetric induction is a key element in asymmetric synthesis.
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| 14. | Homochirality may also result from spontaneous absolute asymmetric synthesis.
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| 15. | Enantiomeric excess is used as one of the indicators of the success of an asymmetric synthesis.
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| 16. | The reaction is also optimized for asymmetric synthesis.
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| 17. | In the Shiina esterification performed under basic conditions, asymmetric synthesis is realized using chiral nucleophilic catalysts.
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| 18. | Applications in asymmetric synthesis have been reported.
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| 19. | Related bidentate phosphine-containing ligands derived from other chiral diamines have also been developed for applications in asymmetric synthesis.
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| 20. | A similar reaction by asymmetric synthesis protected cysteine and potassium tert-butoxide afforded a cyclohexene with 95 % enantiomeric excess:
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