| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7794696 | Carbohydrate Research | 2013 | 9 Pages |
Abstract
- Effect of pentopyranosyl structures on the N-glycosidic torsions is studied.
- Greater rotational freedom around the C1-N1 bond is seen in the arabinosyl analogs as compared to the GlcNAc derivatives.
- Glycosidic torsions are influenced by change in glycan as well as molecular packing.
- Recurrence of antiparallel bilayers in propionamido & chloroacetamido analogs is notable.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Amrita Srivastava, Babu Varghese, Duraikkannu Loganathan,