Asymmetric synthesis of a highly functionalized beta-amino acid: the key amino acid of sperabillins B and D
The asymmetric synthesis of the highly functionalized (3R,5R,6R)-3,6-diamino-5-hydroxyheptanoic acid, the key amino acid fragment of sperabillins B and D, was achieved by an asymmetric Michael addition of lithium (R)-(α-methylbenzyl)allylamide 10 to (E,E)-2,5-heptadienoate establishing the C-3 stere...
Prif Awduron: | Davies, S, Ichihara, O |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
1999
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Eitemau Tebyg
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Total asymmetric synthesis of sperabillins B and D.
gan: Davies, S, et al.
Cyhoeddwyd: (2003) -
ASYMMETRIC-SYNTHESIS OF SYN-ALPHA-ALKYL-BETA-AMINO ACIDS
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Cyhoeddwyd: (1994) -
Asymmetric total synthesis of sperabillins B and D via lithium amide conjugate addition.
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Cyhoeddwyd: (2004) -
Asymmetric synthesis of beta-amino acids via the Michael addition of chiral metal amides
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Cyhoeddwyd: (1997) -
Asymmetric synthesis of beta-amino acid scaffolds
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Cyhoeddwyd: (2001)