Selective deprotection strategies to N-(alpha-methylbenzyl)-beta-amino esters and derived beta lactams
A variety of N,N-diprotected β-amino esters, prepared by highly diastereoselective conjugate addition of chiral lithium amides, were selectively mono-deprotected under either reductive (hydrogenolysis) or oxidative (DDQ or CAN) conditions. Combined with these deprotection methods, lithium (α-methylb...
المؤلفون الرئيسيون: | Davies, S, Ichihara, O |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1998
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مواد مشابهة
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Orthogonal N,N-deprotection strategies of beta-amino esters
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The use of lithium (alpha-methylbenzyl)allylamide for the asymmetric synthesis of unsaturated beta-amino acid derivatives
حسب: Davies, S, وآخرون
منشور في: (1997) -
LITHIUM (ALPHA-METHYLBENZYL)ALLYLAMIDE - A DIFFERENTIALLY PROTECTED CHIRAL AMMONIA EQUIVALENT FOR THE ASYMMETRIC-SYNTHESIS OF BETA-AMINO ACIDS AND BETA-LACTAMS
حسب: Davies, S, وآخرون
منشور في: (1995) -
Asymmetric synthesis of beta-lactams and pseudopeptides via stereoselective conjugate additions of lithium (alpha-methylbenzyl)-allylamide to alpha,beta-unsaturated iron acyl complexes
حسب: Davies, S, وآخرون
منشور في: (1999) -
Conjugate addition to (alpha,beta)(alpha ',beta ')-diendioate esters by lithium (alpha-methylbenzyl)benzylamide: tandem addition-cyclisation versus double addition
حسب: Urones, J, وآخرون
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