Enantioselectivity in the boron aldol reactions of methyl ketones.

DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.

Bibliographic Details
Main Authors: Goodman, J, Paton, R
Format: Journal article
Language:English
Published: Royal Society of Chemistry 2007
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author Goodman, J
Paton, R
author_facet Goodman, J
Paton, R
author_sort Goodman, J
collection OXFORD
description DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.
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spelling oxford-uuid:ee91ca8c-32e9-4384-b94c-d28b1e42c2532022-03-27T11:33:49ZEnantioselectivity in the boron aldol reactions of methyl ketones.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ee91ca8c-32e9-4384-b94c-d28b1e42c253EnglishSymplectic Elements at OxfordRoyal Society of Chemistry2007Goodman, JPaton, RDFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.
spellingShingle Goodman, J
Paton, R
Enantioselectivity in the boron aldol reactions of methyl ketones.
title Enantioselectivity in the boron aldol reactions of methyl ketones.
title_full Enantioselectivity in the boron aldol reactions of methyl ketones.
title_fullStr Enantioselectivity in the boron aldol reactions of methyl ketones.
title_full_unstemmed Enantioselectivity in the boron aldol reactions of methyl ketones.
title_short Enantioselectivity in the boron aldol reactions of methyl ketones.
title_sort enantioselectivity in the boron aldol reactions of methyl ketones
work_keys_str_mv AT goodmanj enantioselectivityintheboronaldolreactionsofmethylketones
AT patonr enantioselectivityintheboronaldolreactionsofmethylketones