1996
DOI: 10.1080/00397919608004580
|View full text |Cite
|
Sign up to set email alerts
|

A Practical Synthesis of ω-Aminoalkanoic Acid Derivatives from Cycloalkanones

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1996
1996
2000
2000

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 10 publications
0
1
0
Order By: Relevance
“…8aminocaprylic acid can be prepared from cyclooctanone (17) by several different Beckman rearrangement strategies (Scheme 8). In this case, the precursor lactam, 2-azacyclononanone (19), was obtained by direct reaction of cyclooctanone with hydroxyamine-O-sulfonic acid, 53 or by initial formation of the cyclooctanone oxime 18 followed by Beckman rearrangement catalyzed by phosphoric, formic, or sulfuric acid. 54 Higher overall yields were often realized from the stepwise procedure.…”
Section: Oral Delivery Of Macromolecular Drugs • 175mentioning
confidence: 99%
“…8aminocaprylic acid can be prepared from cyclooctanone (17) by several different Beckman rearrangement strategies (Scheme 8). In this case, the precursor lactam, 2-azacyclononanone (19), was obtained by direct reaction of cyclooctanone with hydroxyamine-O-sulfonic acid, 53 or by initial formation of the cyclooctanone oxime 18 followed by Beckman rearrangement catalyzed by phosphoric, formic, or sulfuric acid. 54 Higher overall yields were often realized from the stepwise procedure.…”
Section: Oral Delivery Of Macromolecular Drugs • 175mentioning
confidence: 99%