TY - JOUR
T1 - "On-Water"-promoted C-alkylation of indoles with 2-aryl-3-nitro-2H-chromenes under catalyst-free conditions
AU - Habib, Pateliya Mujjamil
AU - Kavala, Veerababurao
AU - Rama Raju, B.
AU - Kuo, Chun Wei
AU - Huang, Wen Chang
AU - Yao, Ching-Fa
PY - 2009/9/1
Y1 - 2009/9/1
N2 - An environmentally benign, method for the synthesis of indolyl(nitro) chromans from indoles and 2-aryl-3-nit:ro-2Hchromenes under catalyst-free conditions by use of an "onwater" concept is described, The salient features of the methodology are its clean, reaction conditions, the eco-friendly medium, and the easy isolation and excellent diastereoselectivities of the products,
AB - An environmentally benign, method for the synthesis of indolyl(nitro) chromans from indoles and 2-aryl-3-nit:ro-2Hchromenes under catalyst-free conditions by use of an "onwater" concept is described, The salient features of the methodology are its clean, reaction conditions, the eco-friendly medium, and the easy isolation and excellent diastereoselectivities of the products,
KW - "on-water" chemistry
KW - 2h-chromenes
KW - Alkylation
KW - Green chemistry
KW - Indoles
KW - Synthetic methods
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U2 - 10.1002/ejoc.200900207
DO - 10.1002/ejoc.200900207
M3 - Article
AN - SCOPUS:69449106910
SP - 4503
EP - 4514
JO - Annalen der Pharmacie
JF - Annalen der Pharmacie
SN - 0075-4617
IS - 26
ER -