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https://doi.org/10.1002/chin.198823335
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Cite Journal: ChemInform |  Publication Date: Jun 7, 1988 |
AbstractIn an effort to reduce the conformational flexibility of the κ‐receptor selective opioid peptide dynorphin A, the cyclic analogues (I) and (II) are synthesized in reasonable yield by the solid phase technique using a protection scheme which permits the cyclization of the peptide still attached to the solid support.
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