| 000 | 01975nam a22003377a 4500 | ||
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| 003 | ZW-GwMSU | ||
| 005 | 20250321112014.0 | ||
| 008 | 250321b |||||||| |||| 00| 0 eng d | ||
| 022 | _a09743626 | ||
| 040 |
_aMSU _bEnglish _cMSU _erda |
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| 050 | 0 | 0 | _aQD31 JOU |
| 100 | 1 |
_aRamazani, Ali _eauthor |
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| 245 | 1 | 0 |
_aSynthesis of N-acylurea derivatives from carboxylic acids and N,N′-dialkyl carbodiimides in water / _ccreated by Ali Ramazani, Fatemeh Zeinali Nasrabadi, Aram Rezaei, Morteza Rouhani, Hamideh Ahankar, Pegah Azimzadeh Asiabi, Sang Woo Joo, Katarzyna Ślepokura and Tadeusz Lis |
| 264 | 1 |
_aBangalore : _bSpringer, _c2105. |
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| 336 |
_2rdacontent _atext _btxt |
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| 337 |
_2rdamedia _aunmediated _bn |
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| 338 |
_2rdacarrier _avolume _bnc |
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| 440 |
_aJournal of chemical sciences _vVolume 127, number,12 |
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| 520 | 3 | _aReactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N , N ′ -dialkyl carbodiimide proceed smoothly at room temperature and in neutral conditions to afford N-acylurea derivatives in high yields. The reaction proceeds smoothly and cleanly under mild conditions and no side reactions were observed. Graphical Abstract Reactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N,N′-dialkylcarbodiimide proceed smoothly at room temperature and in neutral conditions toafford N-acylurea derivatives in high yields, and no side reactions were observed. | |
| 650 |
_a𝑁, 𝑁'-dialkylcarbodiimide _vBenzoic acid derivatives _x(𝐸)-cinnamic acid derivatives |
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| 700 | 1 |
_aNasrabadi, Fatemeh Zeinali _eco author |
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| 700 | 1 |
_aRezaei, Aram _eco author |
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| 700 | 1 |
_aRouhani, Morteza _eco author |
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| 700 | 1 |
_aAhankar, Hamideh _eco author |
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| 700 | 1 |
_aAsiabi, Pegah Azimzadeh _eco author |
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| 700 | 1 |
_aJoo, Sang Woo _eco author |
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| 700 | 1 |
_aŚlepokura, Katarzyna _eco author |
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| 700 | 1 |
_aTadeusz, Lis _eco author |
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| 856 | _uhttps://doi.org/10.1007/s12039-015-0988-6 | ||
| 942 |
_2lcc _cJA |
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| 999 |
_c169438 _d169438 |
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