KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR

The chiral iron acetyl complexes [Fe(CO)(η5-C 5H5)(L)COCH3] [L = PPh3, P(p-tolyl)3] have been kinetically resolved via aldol reactions involving their derived lithium enolates and camphor in the presence of lithium chloride. With (1R)-(+)-camphor the faster reacting iron acetyl enantiomer had the (S...

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Main Authors: Casegreen, S, Costello, J, Davies, S, Heaton, N, Hedgecock, C, Humphreys, V, Metzler, M, Prime, J
格式: Journal article
语言:English
出版: 1994
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author Casegreen, S
Costello, J
Davies, S
Heaton, N
Hedgecock, C
Humphreys, V
Metzler, M
Prime, J
author_facet Casegreen, S
Costello, J
Davies, S
Heaton, N
Hedgecock, C
Humphreys, V
Metzler, M
Prime, J
author_sort Casegreen, S
collection OXFORD
description The chiral iron acetyl complexes [Fe(CO)(η5-C 5H5)(L)COCH3] [L = PPh3, P(p-tolyl)3] have been kinetically resolved via aldol reactions involving their derived lithium enolates and camphor in the presence of lithium chloride. With (1R)-(+)-camphor the faster reacting iron acetyl enantiomer had the (S)-configuration allowing the (R)-iron acetyls to be obtained after recovery of starting material and crystallisation. The corresponding (S)-iron acetyls can be obtained by a base-promoted reverse aldol reaction of the isolated products. A mechanistic rationale for the high enantiomeric discrimination is proposed which involves a chelation-controlled chair transition state with a disfavourable 1 -methyl to cyclopentadienyl interaction in the mismatched pairing.
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spelling oxford-uuid:732a80c4-5205-4382-9a1f-7bc297dba2412022-03-26T19:54:40ZKINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHORJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:732a80c4-5205-4382-9a1f-7bc297dba241EnglishSymplectic Elements at Oxford1994Casegreen, SCostello, JDavies, SHeaton, NHedgecock, CHumphreys, VMetzler, MPrime, JThe chiral iron acetyl complexes [Fe(CO)(η5-C 5H5)(L)COCH3] [L = PPh3, P(p-tolyl)3] have been kinetically resolved via aldol reactions involving their derived lithium enolates and camphor in the presence of lithium chloride. With (1R)-(+)-camphor the faster reacting iron acetyl enantiomer had the (S)-configuration allowing the (R)-iron acetyls to be obtained after recovery of starting material and crystallisation. The corresponding (S)-iron acetyls can be obtained by a base-promoted reverse aldol reaction of the isolated products. A mechanistic rationale for the high enantiomeric discrimination is proposed which involves a chelation-controlled chair transition state with a disfavourable 1 -methyl to cyclopentadienyl interaction in the mismatched pairing.
spellingShingle Casegreen, S
Costello, J
Davies, S
Heaton, N
Hedgecock, C
Humphreys, V
Metzler, M
Prime, J
KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title_full KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title_fullStr KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title_full_unstemmed KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title_short KINETIC RESOLUTION OF THE CHIRAL IRON ACETYL COMPLEXES [FE(CO)(ETA(5)-C5H5)-(L)COCH3] [L=PPH(3), P(P-TOLYL)(3)] VIA ALDOL REACTIONS WITH CAMPHOR
title_sort kinetic resolution of the chiral iron acetyl complexes fe co eta 5 c5h5 l coch3 l pph 3 p p tolyl 3 via aldol reactions with camphor
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