Synthesis of N-(2-hydroxy-3-methoxybenzylidene) - 2, 3, 4, 6-tetra-O-acetyl -β-D galactopyranosylamine as a new chiral Schiff base for asymmetric [2+2] cycloadditions

doi:10.3390/M436

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Molbank 2005, 2005(4), M436; doi:10.3390/M436

Short Note

Synthesis of N-(2-hydroxy-3-methoxybenzylidene) - 2, 3, 4, 6-tetra-O-acetyl -β-D galactopyranosylamine as a new chiral Schiff base for asymmetric [2+2] cycloadditions

A. A. Jarrahpour* , P. Alvand, R. Arab and A. Beheshti

Chemistry Department, College of Sciences, Shiraz University, Shiraz 71454, Iran

* Author to whom correspondence should be addressed.

Received: 2 June 2005 / Accepted: 22 September 2005 / Published: 1 October 2005

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MDPI and ACS Style

Jarrahpour, A.A.; Alvand, P.; Arab, R.; Beheshti, A. Synthesis of N-(2-hydroxy-3-methoxybenzylidene) - 2, 3, 4, 6-tetra-O-acetyl -β-D galactopyranosylamine as a new chiral Schiff base for asymmetric [2+2] cycloadditions. Molbank 2005, 2005, M436.

AMA Style

Jarrahpour AA, Alvand P, Arab R, Beheshti A. Synthesis of N-(2-hydroxy-3-methoxybenzylidene) - 2, 3, 4, 6-tetra-O-acetyl -β-D galactopyranosylamine as a new chiral Schiff base for asymmetric [2+2] cycloadditions. Molbank. 2005; 2005(4):M436.

Chicago/Turabian Style

Jarrahpour, A. A.; Alvand, P.; Arab, R.; Beheshti, A. 2005. "Synthesis of N-(2-hydroxy-3-methoxybenzylidene) - 2, 3, 4, 6-tetra-O-acetyl -β-D galactopyranosylamine as a new chiral Schiff base for asymmetric [2+2] cycloadditions." Molbank 2005, no. 4: M436.

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