## Abstract From ^1^H‐ and ^13^C‐NMR. data, a crown conformation with __trans__ amide bonds is deduced for 1,6‐diaza‐2,7‐cyclodecadione (**1**) in solution. Compound **1** was obtained by reaction of 2‐pyrrolidone with POCl~3~.
The conformation of 1,6-anhydrolactose and its hexa-acetate in solution
✍ Scribed by Alfonso Rivera-Sagredo; Jesús Jiménez-Barbero
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 857 KB
- Volume
- 215
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
The conformation of 1,6-anhydrolactoase (1) has been investigated by n.m.r. spectroscopy and molecular mechanics calculations. For a solution in D2O, the 1,6-anhydroglucopyranoid ring has a 1C4 conformation, whereas there is a approximately 1:1 equilibrium between the 1C4 and the BO,3 conformations in (CD3)2SO. There is restricted flexibility with phi -80 +/- 20 degrees and psi -120 +/- 40 degrees. The hexa-acetate (2) of 1 shows a similar conformational behaviour.
📜 SIMILAR VOLUMES
## Abstract The data (TABLES I and 2) extracted from the ^1^H‐nmr spectra of X‐206 (1) and its sodium salt confirm the unique conformation reported for the solid state 1a and which is found to be identical in bulk Solution (Figure 7). The backbone of the antibiotic follows the seam of a tennis ball