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
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| Format: | Citation Index Journal |
| Published: |
2008
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| Online Access: | http://eprints.utp.edu.my/7859/1/mjc8_052_056ceciliadw.pdf http://eprints.utp.edu.my/7859/ |
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| Summary: | 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 |
|---|