| 000 | a | ||
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| 999 |
_c19302 _d19302 |
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| 003 | OSt | ||
| 005 | 20230504141353.0 | ||
| 008 | 230504b xxu||||| |||| 00| 0 eng d | ||
| 040 |
_aAIKTC-KRRC _cAIKTC-KRRC |
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| 100 |
_920678 _aPaira, Moumita |
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| 245 | _aPPh3-Catalyzed Intramolecular Cyclization of hydroxypropargylamides: Synthesis of Structurally Diverse Morpholinone Derivatives | ||
| 250 | _aVol.61(9), Sep | ||
| 260 |
_aNew Delhi _bCSIR _c2022 |
||
| 300 | _a1014-1024p. | ||
| 520 | _aThe metal-free synthesis of functionalized morpholinones through a sequential intramolecular post-ugi cyclization strategy is described. In the subsequent step, Ugi adducts hydroxypropargylamides derivative undergoes chemo- and regioselective 6-exo-dig catalytic cyclization to afford O-cyclized product in the presence of triphenylphosphine. This sequence offers an engrossing functionalized morpholinones scaffolds involving moderate reaction conditions with broad substrate scopes and moderate to good yields. | ||
| 650 | 0 |
_95009 _aGENERAL CHEMISTRY |
|
| 773 | 0 |
_tIndian journal of chemistry (Section B) _dNew Delhi NISCAIR-CSIR 2005 _x0019-5103 |
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| 856 |
_uhttp://op.niscpr.res.in/index.php/IJC/article/view/59955 _yClick here |
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| 942 |
_2ddc _cAR |
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