TY - JOUR
T1 - Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes
AU - Habib, Pateliya Mujjamil
AU - Kavala, Veerababurao
AU - Kuo, Chun Wei
AU - Yao, Ching Fa
N1 - Funding Information:
Financial support of this work by the National Science Council of the Republic of China and National Taiwan Normal University (TOP001) is gratefully acknowledged.
PY - 2008/12/1
Y1 - 2008/12/1
N2 - A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.
AB - A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.
UR - http://www.scopus.com/inward/record.url?scp=54049093542&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=54049093542&partnerID=8YFLogxK
U2 - 10.1016/j.tetlet.2008.09.109
DO - 10.1016/j.tetlet.2008.09.109
M3 - Article
AN - SCOPUS:54049093542
VL - 49
SP - 7005
EP - 7007
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 49
ER -