𝔖 Bobbio Scriptorium
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Theoretical studies on conformational isomerism of bifurans and bipyrroles

✍ Scribed by E. Ortí; F. Tomás; J. Sánchez-Marín


Book ID
119115845
Publisher
Elsevier Science
Year
1983
Tongue
English
Weight
565 KB
Volume
104
Category
Article
ISSN
0166-1280

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📜 SIMILAR VOLUMES


A quantum-mechanical study on the stereo
✍ V. Galasso; N. Trinajstić 📂 Article 📅 1972 🏛 Elsevier Science 🌐 French ⚖ 656 KB

most probable conformational arrangements of isomeric bipyrroks, bifurans, bithiophenes, thienylfurans, and biselenophenes have been investigated using the Extended Hflckel MO approach. The barrier heights between the syn and anti forms decrease sharply on going along the series bifurans bithiophene

Conformational studies of proteoglycans:
✍ M. Nagarajan; V. S. R. Rao 📂 Article 📅 1979 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 692 KB

## Abstract Various models proposed for heparin have been examined by a stereochemical approach involving contact distance criteria and potential energy calculations. The present study suggests that the model favored by Atkins and coworkers [__Biochem. J.__ (1973) **135**, 729–733 and (1974) **143*