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Number of results

Journal

2014 | 12 | 3 | 416-425

Article title

Enantioselective Michael additions of aldehydes to nitroalkenes catalyzed with ionically tagged organocatalyst

Content

Title variants

Languages of publication

EN

Abstracts

EN
Enantioselective organocatalytic Michael additions affords useful building blocks for many biologically and medicinally relevant compounds. Ionically-tagged diphenylprolinol silyl ether efficiently catalyzes several Michael additions of aldehydes to nitroalkenes in ionic liquids. The Michael additions work well in ionic liquids; yields up to 95% and enantioselectivities up to 95% ee were achieved. Furthermore, in some cases, the catalytic system was reusable.

Publisher

Journal

Year

Volume

12

Issue

3

Pages

416-425

Physical description

Dates

published
1 - 3 - 2014
online
21 - 12 - 2013

Contributors

  • Comenius University in Bratislava
author
  • Synkola

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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11532-013-0391-4
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