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0342348662
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The stereochemical assignments were corroborated by independent syntheses from enantiopure components
-
The stereochemical assignments were corroborated by independent syntheses from enantiopure components.
-
-
-
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24
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0002563284
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and references cited therein; see also ref, 8
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0342783725
-
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note
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3, at 25 °C, with a 600 MHz Bruker AMX-600 spectrometer.
-
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28
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84986437005
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Johnson W.C., Jr.1
-
30
-
-
0342348660
-
-
The CD spectrum of the natural tetrapeptide showed much diminished absorption at 220 nm
-
The CD spectrum of the natural tetrapeptide showed much diminished absorption at 220 nm.
-
-
-
-
31
-
-
0342348659
-
-
For clarity, the radical is shown as a singly-occupied p-orbital, which could be delocalized into the carbonyl group of the amide
-
For clarity, the radical is shown as a singly-occupied p-orbital, which could be delocalized into the carbonyl group of the amide.
-
-
-
-
32
-
-
0002071299
-
-
For recent examples concerning conformational aspects of β-amino acid constituted oligomers, see a) Fernández-Santin, J. M.; Munoz-Guerra, S.; Rodriguez-Gálan, A.; Aymami, J.; Lloveras, J.; Subirana, J.A.; Giralt, E.; Ptak, M. Macromolecules 1987, 20, 62;
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0029953285
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