2011
DOI: 10.1007/s11172-011-0250-4
|View full text |Cite
|
Sign up to set email alerts
|

Nucleophilic substitution of the acetoxy group in 3-methylbenzoylaminomethyl acetate

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2012
2012
2022
2022

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 13 publications
0
1
0
Order By: Relevance
“…Aside from the highlighted application in Scheme A (pyrazole 1 ), a small selection of additional known compounds were targeted, such as pyrazoles 70 – 72 (Scheme A). Hemiaminals 70 and 71 could be accessed in high yields in one simple step versus the multistep procedures used in the past. Finally, the tert- butylated pyrazole 72 could be accessed in a single step (although in low yield due to an extended reaction time needed with pivalic acid).…”
mentioning
confidence: 99%
“…Aside from the highlighted application in Scheme A (pyrazole 1 ), a small selection of additional known compounds were targeted, such as pyrazoles 70 – 72 (Scheme A). Hemiaminals 70 and 71 could be accessed in high yields in one simple step versus the multistep procedures used in the past. Finally, the tert- butylated pyrazole 72 could be accessed in a single step (although in low yield due to an extended reaction time needed with pivalic acid).…”
mentioning
confidence: 99%