Abstract
1,1-Diacyloxy-1-phenylmethanes and 1-pivaloxy-1-acyloxy-1-phenylmethanes have been used as bench stable N-acylating reagents for primary and secondary amines and anilines under solvent-free conditions to afford their corresponding amides in good yield.
Language | English |
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Number of pages | 10 |
Journal | Tetrahedron |
Early online date | 21 May 2018 |
DOIs | |
Status | E-pub ahead of print - 21 May 2018 |
Fingerprint
Keywords
- 1,1-Acylals
- Amides
- N-Acylation
- Solvent free
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Cite this
1,1-Diacyloxy-1-phenylmethanes as versatile N-acylating agents for amines. / Chapman, Robert S.L.; Tibbetts, Joshua D.; Bull, Steven D.
In: Tetrahedron, 21.05.2018.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - 1,1-Diacyloxy-1-phenylmethanes as versatile N-acylating agents for amines
AU - Chapman, Robert S.L.
AU - Tibbetts, Joshua D.
AU - Bull, Steven D.
PY - 2018/5/21
Y1 - 2018/5/21
N2 - 1,1-Diacyloxy-1-phenylmethanes and 1-pivaloxy-1-acyloxy-1-phenylmethanes have been used as bench stable N-acylating reagents for primary and secondary amines and anilines under solvent-free conditions to afford their corresponding amides in good yield.
AB - 1,1-Diacyloxy-1-phenylmethanes and 1-pivaloxy-1-acyloxy-1-phenylmethanes have been used as bench stable N-acylating reagents for primary and secondary amines and anilines under solvent-free conditions to afford their corresponding amides in good yield.
KW - 1,1-Acylals
KW - Amides
KW - N-Acylation
KW - Solvent free
UR - http://www.scopus.com/inward/record.url?scp=85048338873&partnerID=8YFLogxK
U2 - 10.1016/j.tet.2018.05.044
DO - 10.1016/j.tet.2018.05.044
M3 - Article
JO - Tetrahedron
T2 - Tetrahedron
JF - Tetrahedron
SN - 0040-4020
ER -