Journal
ORGANIC LETTERS
Volume 21, Issue 8, Pages 2574-2577Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b00534
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [21472107, 21372142]
Ask authors/readers for more resources
A new method for the Bischler-Napieralski-type synthesis of 3,4-dihydroisoquinolines was developed by a Tf2O-promoted tandem annulation from phenylethanols and nitriles. Its success was mainly due to the fact that a phenonium ion was formed in the process and practically functioned as a stable and reactive primary phenylethyl carbocation.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
