The polymorphic behavior of the three series of tris-homoacyl (C14:0 , C 16:0 and C 18:0) cyclopentane-l,2,3-triol analogs of the natural saturated triglycerides has been studied using differential thermal analysis, Fourier transform infrared spectroscopy, and X-ray diffraction. It was found that th
A study of the fragmentation of cyclopentane-1,3-diols and of cyclopentane-1,2,4-triols
✍ Scribed by Gérard A. Singy; A. Buchs
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 421 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1076-5174
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pentanediol, 2-methyl-1,3-cyclohexanediol and 2-t.butyl-1,3-cyclohexanediol have been prepared. Configurational assignment and some conformational aspects are described. The diastereomers of 2-methyl-l,3-~yclopentanediol, 2-t.buty1-1.3-cyclo-
## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract The conformations of __cis__‐ (**1**) and __trans__‐cyclopentane‐1,3‐diol (**2**) have been studied by __ab initio__ (Gaussian 98) and molecular mechanics (PCMODEL) calculations and by NMR spectroscopy. The calculations gave two low‐energy conformations for (**1**), **1A** and **1B**, b