TY - JOUR
T1 - Cascade bicyclization of triethylammonium thiolates with hydrazines
T2 - Efficient access to pyrazolo[3,4-: C] quinolines
AU - Fan, Wei
AU - Li, Yan Rong
AU - Jiang, Bo
AU - Li, Guigen
N1 - Funding Information:
We are grateful for financial support from the NSFC (No. 21332005), PAPD of Jiangsu Higher Education Institutions, Robert A. Welch Foundation (D-1361, USA) and NIH (R33DA031860, USA), and NSF of Jiangsu Province (BK20151163).
Publisher Copyright:
© The Royal Society of Chemistry 2016.
PY - 2016
Y1 - 2016
N2 - A new bicyclization strategy has been established, allowing a flexible and practical approach to 33 examples of pyrazolo[3,4-c]quinolines from low-cost and readily accessible triethylammonium thiolates with hydrazines. Notably, the features of this work include broad functional group compatibility, mild reaction conditions and good reaction yields.
AB - A new bicyclization strategy has been established, allowing a flexible and practical approach to 33 examples of pyrazolo[3,4-c]quinolines from low-cost and readily accessible triethylammonium thiolates with hydrazines. Notably, the features of this work include broad functional group compatibility, mild reaction conditions and good reaction yields.
UR - http://www.scopus.com/inward/record.url?scp=84989233190&partnerID=8YFLogxK
U2 - 10.1039/c6ob01728b
DO - 10.1039/c6ob01728b
M3 - Article
AN - SCOPUS:84989233190
VL - 14
SP - 9080
EP - 9087
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 38
ER -