Autor: |
Février FC; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, USA., Smith ED, Comins DL |
Jazyk: |
angličtina |
Zdroj: |
Organic letters [Org Lett] 2005 Nov 24; Vol. 7 (24), pp. 5457-60. |
DOI: |
10.1021/ol052196j |
Abstrakt: |
[reaction: see text] Regioselective deprotonations of (S)-nicotine and derivatives at the C-2 and C-6 positions of the pyridine ring were performed in good to excellent yields. These methodologies allow the direct introduction of a plethora of functional groups onto the pyridine ring of nicotine. |
Databáze: |
MEDLINE |
Externí odkaz: |
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