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: | |
|---|---|
| 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!
|
| id |
my.utp.eprints.7859 |
|---|---|
| record_format |
eprints |
| spelling |
my.utp.eprints.78592017-01-19T08:26:47Z 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 Wilfred, Cecilia QD Chemistry 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 2008 Citation Index Journal PeerReviewed application/pdf http://eprints.utp.edu.my/7859/1/mjc8_052_056ceciliadw.pdf Wilfred, Cecilia (2008) 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. [Citation Index Journal] http://eprints.utp.edu.my/7859/ |
| institution |
Universiti Teknologi Petronas |
| building |
UTP Resource Centre |
| collection |
Institutional Repository |
| continent |
Asia |
| country |
Malaysia |
| content_provider |
Universiti Teknologi Petronas |
| content_source |
UTP Institutional Repository |
| url_provider |
http://eprints.utp.edu.my/ |
| topic |
QD Chemistry |
| spellingShingle |
QD Chemistry Wilfred, Cecilia 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 |
| description |
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 |
| format |
Citation Index Journal |
| author |
Wilfred, Cecilia |
| author_facet |
Wilfred, Cecilia |
| author_sort |
Wilfred, Cecilia |
| title |
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 |
| title_short |
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 |
| title_full |
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 |
| title_fullStr |
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 |
| title_full_unstemmed |
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 |
| title_sort |
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 |
| publishDate |
2008 |
| url |
http://eprints.utp.edu.my/7859/1/mjc8_052_056ceciliadw.pdf http://eprints.utp.edu.my/7859/ |
| _version_ |
1738655609102794752 |
| score |
13.188404 |