ChemInform Abstract: Asymmetric Rearrangement of Racemic Epoxides Catalyzed by Chiral Broensted Acids
The chiral Broensted acid catalyzed asymmetric 1,2‐rearrangement of racemic epoxides (I) and (III) via a hydrogen‐shift process is described.
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| Veröffentlicht in: | ChemInform 2013-07, Vol.44 (28), p.no-no |
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| container_title | ChemInform |
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| creator | Zhuang, Minyang Du, Haifeng |
| description | The chiral Broensted acid catalyzed asymmetric 1,2‐rearrangement of racemic epoxides (I) and (III) via a hydrogen‐shift process is described. |
| doi_str_mv | 10.1002/chin.201328025 |
| format | Article |
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| ispartof | ChemInform, 2013-07, Vol.44 (28), p.no-no |
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| language | eng |
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| source | Wiley Online Library All Journals |
| subjects | Acids alcohols (benzene compounds) diastereoselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) enantioselective syntheses (incl. cis/trans-isomerism) rearrangements |
| title | ChemInform Abstract: Asymmetric Rearrangement of Racemic Epoxides Catalyzed by Chiral Broensted Acids |
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