A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM

Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subject to double stereodifferentiation, the mismatched pair reaction allowing access to an intermediate for 1β-methylcarbapenem synthesis. © 1995.

Bibliographic Details
Main Authors: Davies, S, Hedgecock, C, Mckenna, J
Format: Journal article
Language:English
Published: 1995
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author Davies, S
Hedgecock, C
Mckenna, J
author_facet Davies, S
Hedgecock, C
Mckenna, J
author_sort Davies, S
collection OXFORD
description Conjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subject to double stereodifferentiation, the mismatched pair reaction allowing access to an intermediate for 1β-methylcarbapenem synthesis. © 1995.
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spelling oxford-uuid:9e1d5438-aebc-40d5-b2e9-a3f7c2a0f4972022-03-27T00:47:44ZA STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEMJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9e1d5438-aebc-40d5-b2e9-a3f7c2a0f497EnglishSymplectic Elements at Oxford1995Davies, SHedgecock, CMckenna, JConjugate addition of lithium N-allyl-N-α-methylbenzylamide to chiral α,β-unsaturated esters is subject to double stereodifferentiation, the mismatched pair reaction allowing access to an intermediate for 1β-methylcarbapenem synthesis. © 1995.
spellingShingle Davies, S
Hedgecock, C
Mckenna, J
A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title_full A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title_fullStr A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title_full_unstemmed A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title_short A STEREOCONTROLLED APPROACH TO 1-BETA-METHYLCARBAPENEM
title_sort stereocontrolled approach to 1 beta methylcarbapenem
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