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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1969 Mar;62(3):650–652. doi: 10.1073/pnas.62.3.650

FLEXIBILITY OF SUPPOSED “RIGID” MOLECULES: SUBSTITUTED 2,5-PIPERAZINEDIONES (DIKETOPIPERAZINES)

E Benedetti 1, P Corradini 1, M Goodman 1, C Pedone 1
PMCID: PMC223646  PMID: 16591734

Abstract

The relevant results of accurate X-ray analyses of both the trans-and the L-cis-3,6-dimethyl-2,5-piperazinediones (diketopiperazines) are reported. We note that a large variability of conformations for the ring system can be accomplished by coupling small bond-angle deformations with large variations of the internal rotation angles. The experimental molecular models are discussed in terms of these changes and in terms of nonbonded intramolecular interactions.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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