Direct versatile route to conformationally constrained glutamate analogues
Novel conformationally constrained glutamate analogues are readily available from (S)-pyroglutamic acid; using a bicyclic lactam template, diastereocontrolled and sequential modification of the pyrrolidine ring is possible, allowing a versatile access to several glutamate and kainoid analogues; vari...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
1998
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