Journal article
Enantioselectivity in the boron aldol reactions of methyl ketones.
- Abstract:
- DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Authors
- Publisher:
- Royal Society of Chemistry
- Journal:
- Chemical Communications More from this journal
- Issue:
- 21
- Pages:
- 2124-2126
- Publication date:
- 2007-06-01
- DOI:
- EISSN:
-
1364-548X
- ISSN:
-
1359-7345
- Language:
-
English
- Pubs id:
-
pubs:117457
- UUID:
-
uuid:ee91ca8c-32e9-4384-b94c-d28b1e42c253
- Local pid:
-
pubs:117457
- Source identifiers:
-
117457
- Deposit date:
-
2012-12-19
Terms of use
- Copyright holder:
- Royal Society of Chemistry
- Copyright date:
- 2007
- Notes:
- This journal is © The Royal Society of Chemistry 2007. The full text of this article is not available in ORA. You may be able to access the article via the publisher copy link above.
If you are the owner of this record, you can report an update to it here: Report update to this record