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.

গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক: Goodman, J, Paton, R
বিন্যাস: Journal article
ভাষা:English
প্রকাশিত: 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