Stille Coupling and One-pot Reduction-Deprotection Sequence in Preparing Z-3-(2-Amino-phenyl)-prop-2-en-1-ol, a Precursor in Quinoline Synthesis
Stille coupling on N-(2-iodo-phenyl)-acetamide followed by reduction-deprotection sequence has been utilised to prepare Z-3-(2-amino-phenyl)-prop-2-en-1-ol (1). Consequently, tandem oxidation processes on Z
Saved in:
Main Author: | Wilfred, Cecilia |
---|---|
Format: | Citation Index Journal |
Published: |
2008
|
Subjects: | |
Online Access: | http://eprints.utp.edu.my/7859/1/mjc8_052_056ceciliadw.pdf http://eprints.utp.edu.my/7859/ |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
(E)-3-[4-(Hexyloxy)phenyl]-1-(2-hydroxyphenyl)prop-2-en-1-on
by: Zainab, Ngaini, et al.
Published: (2009) -
(E)-1-[4-(Hexyloxy)phenyl]-3-(2-hydroxyphenyl) prop-2-en-1-one
by: Siti Muhaini, Haris Fadzillah, et al.
Published: (2012) -
(E)-3-[4-(Hexyloxy)phenyl]-1-(2-hydroxyphenyl)prop-2-en-1-one
by: Zainab, Ngaini, et al.
Published: (2009) -
(E)-3-[4-(Dodecyloxy)phenyl]-1-(2-hydroxyphenyl)prop-2-en-1-one
by: Zainab, Binti Ngaini, et al.
Published: (2009) -
1-[4-(Prop-2-en-1-yloxy)benzyl]-2-[4-(prop-2-en-1-yloxy)phenyl]-1H benzimidazole
by: Hegde, Gurumurthy, et al.
Published: (2012)