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Conformational preferences of Ac-ΔAla-NMe2 and Ac-(Z)-ΔPhe-NMe2 were studied and compared with those of their monomethyl counterparts as well as with those of their saturated analogues. X-Ray data and energy calculations revealed a highly conservative conformation of the dehydro dimethylamides, which is located in a high-energy region of the Ramachandran map.
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Opis fizyczny
p.1179-1183,fig.
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autor
- University of Opole, 48 Oleska str., 45-052 Opole, Poland
autor
autor
autor
autor
Bibliografia
- 1.Palmer, D.E., Pattaroni, Ch., Nunami, K., Chadha, R.K., Goodman, M., Wakamiya, T., Fukase, K., Horimoto, S., Kitazawa, M., Fujita, H., Kubo, A. & Shiba, T .(1992). J. Am. Chem. Soc. 114, 5634-5642.
- 2.Souhassou, M., Lecomte, C., Ghermani, N.-E., Rohmer, M.M., Wiest, R., Benard, M. & Blessing, R.H. (1992) J. Am. Chem. Soc. 114, 2371-2382.
- 3.Zimmerman, S.S., Pottle, M.S., Nemethy, G. & Scheraga,H.A. (1977) Macromolecules 10, 1-9. MEDLINE
- 4.Dunitz, J.D. & Winkler, F.K. (1975) Acta Crystallogr. B31, 251-263.
Typ dokumentu
Bibliografia
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Identyfikator YADDA
bwmeta1.element.agro-article-92b2feff-0a62-4f64-ae26-b85f89a29793