Premium
Conformational analysis of N ‐acylazabicyclooctanes
Author(s) -
Sohár P.,
Pelczer I.,
Váczi I.,
Tombor A.,
Matolcsy G.
Publication year - 1985
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260230705
Subject(s) - chemistry , conformational isomerism , substituent , amide , octane , nuclear magnetic resonance spectroscopy , dept , stereochemistry , solvent , computational chemistry , organic chemistry , molecule
N ‐Acyl derivatives of 1,3,3‐trimethyl‐6‐azabicyclo[3.2.1]octane were synthesized as compounds with potential pesticidal activity. The conformation of the starting compound and the substituent dependence of the amide rotamers of the acyl derivatives were studied by 1 and 13 C NMR spectroscopy, making use of solvent effects (ASIS) and DR, DNOE and DEPT measurements.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom