Direct NMR evidence of the axial preference of the substituent on phosphorus in 2-chloro- and 2-methoxy-1,2,3-dioxaphosphorinanes.

Tetrahedron Letters

Volumn 12, Issue 5, 1971, Pages 461-464

  Haemers, M ^a   Ottinger, R ^a   Reisse, J ^a   Zimmermann, D ^a  

^a UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0343080553     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)96468-8     Document Type: Article

References (14)

1. Configurations and conformations of the geometrical isomers of 2-ethoxy-4-methyl-1,3,2-dioxaphosphorinane
2. NMR and conformations of some 5--butyl-2-methoxy- and 2-chloro-1,3,2-dioxaphosphorinanes
3. Stereochemistry at phosphorus in a six-membered ring phosphite
4. Possible importance of lone pair interactions in the preferred axial orientation of phenyl in a 6-membered ring phenylphosphonite
5. The conformation of non-aromatic ring compounds. Part 35: Trimethylene Sulfite and Related Compounds
6. NMR experiments on ketals VI. PMR spectra of alkyl substituted 1, 3-dioxanes with rigid or anancomeric structures
7. Crystal and molecular structure of 5-t-butyl-2-methyl-2-oxo-1,3,2-dioxaphosphorinan (C8H17PO3)