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Synthesis of (2R,3S)-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl) 2-(4-bromophenyl)-3-(tert-butoxy-carbonylamino)-tetrahydrofuran-3-carboxylate and (2S,3R)-((1R,2S,5R)-2-isopropyl- 5-methylcyclohexyl)2-(4- bromophenyl)-3-(tert-butoxy¬carbonyl¬amino)-tetrahydrofuran-3-carboxylate
Molbank 2009, 2009(1), M595; doi:10.3390/M595
Short Note

Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea

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Received: 7 January 2009 / Accepted: 13 March 2009 / Published: 18 March 2009
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Abstract: An unexpected product, 1-[(2-oxonaphthalen-1(2H)-ylidene)methyl]urea 4 of the condensation reaction of 2-hydroxy-1-naphthaldehyde with or without ethyl benzoylacetate and urea under hydrochloric acid-catalyzed and solvent-free conditions is reported.
Keywords: 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea; Condensation reaction Solvent-free conditions 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea; Condensation reaction Solvent-free conditions
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MDPI and ACS Style

Xu, J.; Chen, A.; Liu, Q. Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea. Molbank 2009, 2009, M595.

AMA Style

Xu J, Chen A, Liu Q. Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea. Molbank. 2009; 2009(1):M595.

Chicago/Turabian Style

Xu, Jiehua; Chen, Anjun; Liu, Qingjian. 2009. "Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea." Molbank 2009, no. 1: M595.

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