𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Theoretical study on the stable conformers of 1,3-diazetidine

✍ Scribed by J. Catalán; O. Mó; P. Pérez; M. Yáñez

Book ID
119116227
Publisher
Elsevier Science
Year
1984
Tongue
English
Weight
420 KB
Volume
106
Category
Article
ISSN
0166-1280

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Crystal structure and theoretical invest
Crystal structure and theoretical investigation of the configurations of 1,3-dichloro-1,3-diazetidine-2,4-dione and 1,3-bis(trimethylsilyl)-1,3-diazetidine-2,4-dione
✍ Ferdinand Belaj; Edgar Nachbaur; Gottfried Faleschini; Rudolf Janoschek 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 582 KB

## Crystal structures o f 1 ,3-dichloro-l,3-diazetidine-2,4dione (1) and the hitherto unknown compound 1,3bis(trimethylsilyl)-1,3-diazetidine-2,4-dione (2) have been determined by X-ray crystallography: 1: (CINCO),,

Interconversions of Z-1,3,5-hexatriene c
Interconversions of Z-1,3,5-hexatriene conformers: A theoretical study
✍ Debora Henseler; Rupert Rebentisch; Georg Hohlneicher 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 351 KB 👁 1 views

A two-dimensional potential-energy surface was calculated for the ground state of Z-1,3,5-hexatriene in order to study the conformational relaxation after its photochemical formation from 1,3-cyclohexadiene. The potential-energy surface was scanned along both C-C single bond torsional angles while a

Conformational studies of proteoglycans:
Conformational studies of proteoglycans: Theoretical studies on the conformation of heparin
✍ 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*