Journal article
ASYMMETRIC-SYNTHESIS OF R-BETA-AMINO BUTANOIC ACID AND S-BETA-TYROSINE - HOMOCHIRAL LITHIUM AMIDE EQUIVALENTS FOR MICHAEL ADDITIONS TO ALPHA,BETA-UNSATURATED ESTERS
- Abstract:
- Michael addition of the lithium amide derived from R-N-(α-methylbenzyl)benzylamine to benzyl E-crotonate is highly stereoselective (95% d.e.) giving after debenzylation and crystallisation homochiral R-β-amino butanoic acid. A similar addition to methyl E-(p-benzyloxy)cinnamate is completely stereoselective giving after debenzylation and acid hydrolysis homochiral S-β-tyrosine as its HCl salt. © 1993.
- Publication status:
- Published
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- Publisher copy:
- 10.1016/S0957-4166(00)82354-X
Authors
- Journal:
- TETRAHEDRON-ASYMMETRY More from this journal
- Volume:
- 2
- Issue:
- 3
- Pages:
- 183-186
- Publication date:
- 1991-01-01
- DOI:
- EISSN:
-
1362-511X
- ISSN:
-
0957-4166
- Pubs id:
-
pubs:110747
- UUID:
-
uuid:346bcda7-4229-4f95-84e6-b21d1f3ce1c4
- Local pid:
-
pubs:110747
- Source identifiers:
-
110747
- Deposit date:
-
2012-12-19
- ARK identifier:
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- Copyright date:
- 1991
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