Magnetic anisotropy of the oximido group. Additional proof of greater deshielding from proximity of the hydroxyl group

Huitric, Alain C.; Roll, David B.; DeBoer, John R.

doi:10.1021/jo01280a102

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1968

1985

Publication Types

Select...

Article5

Other1

Relationship

Self Cite0

Independent6

Authors

Journals

Cited by 22 publications

(1 citation statement)

References 1 publication

(1 reference statement)

Supporting

Mentioning

Contrasting

Order By: Relevance

“…8.17 ± 0.11 (13) 8.67 ± 0.24d (7) (S)-H-IO "Compounds 4 and 11 were tested as oxalates whereas 10 and its enantiomers were tested as 0.5 fumarates. 6pA2 ± standard error, with the number of experimental values in parentheses.…”

mentioning

confidence: 99%

New chiral and isomeric cyclopropyl ketoxime propanolamine derivatives with potent .beta.-adrenergic blocking properties

Bouzoubaa¹,

Leclerc²,

Rakhit³

et al. 1985

J. Med. Chem.

View full text Add to dashboard Cite

The synthesis of R-(+) and S-(-) isomers of O-[3-tert-butylamino)-2-hydroxypropyl] cyclopropyl methyl ketone oxime (falintolol) is described. The syn and anti isomers of falintolol were obtained in two different ways from cyclopropyl methyl ketoxime or from falintolol. For comparison purposes, the enantiomers of the dicyclopropyl ketone oxime derivatives were also prepared. Structure-activity relationships are described.

show abstract

mentioning

confidence: 99%