The remarkable effect of the 7-substituent in the diastereoselective oxidative rearrangement of indoles: asymmetric synthesis of 3,3-disubstituted oxindoles
The nature of the 7-substituent has a remarkable effect on the diastereoselectivity of the oxidative rearrangement of indole-2-carboxamides derived from (S)-2-methoxymethylpyrrolidine into chiral 3,3-disubstituted oxindoles.
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2007-01 (3), p.286-288 |
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| container_title | Chemical communications (Cambridge, England) |
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| creator | Lachia, Mathilde Poriel, Cyril Slawin, Alexandra M Z Moody, Christopher J |
| description | The nature of the 7-substituent has a remarkable effect on the diastereoselectivity of the oxidative rearrangement of indole-2-carboxamides derived from (S)-2-methoxymethylpyrrolidine into chiral 3,3-disubstituted oxindoles. |
| doi_str_mv | 10.1039/b613716d |
| format | Article |
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| ispartof | Chemical communications (Cambridge, England), 2007-01 (3), p.286-288 |
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| language | eng |
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| source | Royal Society of Chemistry Journals Archive (1841-2007); Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Chemical Physics Chemical Sciences Organic chemistry Physics |
| title | The remarkable effect of the 7-substituent in the diastereoselective oxidative rearrangement of indoles: asymmetric synthesis of 3,3-disubstituted oxindoles |
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