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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

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Publisher copy:
10.1039/b704786j

Authors


Goodman, JM More by this author
Publisher:
Royal Society of Chemistry Publisher's website
Journal:
Chemical communications (Cambridge, England) More in this journal
Issue:
21
Pages:
2124-2126
Publication date:
2007-06-19
DOI:
EISSN:
1364-548X
ISSN:
1359-7345
URN:
uuid:ee91ca8c-32e9-4384-b94c-d28b1e42c253
Source identifiers:
117457
Local pid:
pubs:117457
Language:
English

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