2012
DOI: 10.1134/s1070428012100053
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of acetals containing a primary amino group

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
2

Relationship

1
1

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 6 publications
0
2
0
Order By: Relevance
“…Yield Recrystallization of the still residue from hexane gave acetal 2a. Yield 1.91 g (56%), mp 55-56°C; published data [14]: mp 55-57°C.…”
Section: 22-trifluoro-n-[2-methyl-3-(vinyloxy)propan-2-yl]acetamidmentioning
confidence: 99%
See 1 more Smart Citation
“…Yield Recrystallization of the still residue from hexane gave acetal 2a. Yield 1.91 g (56%), mp 55-56°C; published data [14]: mp 55-57°C.…”
Section: 22-trifluoro-n-[2-methyl-3-(vinyloxy)propan-2-yl]acetamidmentioning
confidence: 99%
“…The elemental analyses were obtained on a Flash EA 1112 analyzer. N- ethyl]-and N- [3-(vinyloxy)propyl]-2,2,2-trifluoroacetamides 1a and 1c were synthesized as described in [14].…”
Section: Nn′-[ethane-11-diylbis(oxyethane-21-diyl)]bis-(222-trifmentioning
confidence: 99%