| | 1 | Author
| A. O., W.J S | Requires cookie* | | | Title
| Axial Preference of Methylthio Substituent in Dioxaphosphorinanyl Ring System  | | | | Abstract
| The spatial disposition of a 2-methvlthio group in the 4-m ethyl-1,3,2-dioxaphosphorin anyl ring system was studied by stereochemical correlation, X H, 13C and 31P NMR. It has been established that a CH3S-group prefers an axial orientation much more strongly than does a m ethoxy group. | | | |
Reference
| (Z. Naturforsch. 30b, 430—436 [1975]; received February 4 1975) | | | |
Published
| 1975 | | | |
Keywords
| ) 2-Methylthio-l, 3, 2-dioxaphosphorinans, Synthesis, Spectral Characteristics, Conformation | | | |
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| default:Reihe_B/30/ZNB-1975-30b-0430.pdf | | | | Identifier
| ZNB-1975-30b-0430 | | | | Volume
| 30 | |
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