Abstract
The absolute stereochemistry of the recovered nitroallylic acetates 1 and double bond geometry in the products 3-5 in our original paper were misassigned.[1] The correct chemical structures and stereochemistry for reactions in the presence of either catalyst 2b or 14c are shown in Scheme 1 and Figure 2. Subsequently, corrections of the chemical structure and stereochemistry should be made in the paper accordingly and new Supporting Information is provided. The authors apologize for any inconvenience caused.
Original language | English |
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Pages (from-to) | 655 |
Number of pages | 1 |
Journal | European Journal of Organic Chemistry |
Volume | 2015 |
Issue number | 3 |
DOIs |
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Publication status | Published - 2015 Jan |
Keywords
- Aldehydes
- Diastereoselectivity
- Enantioselectivity
- Ketones
- Kinetic resolution
- Organocatalysis
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry