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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
88086-86-6

4-Hydroxybenzaldehyde rhamnoside synthesis

7synthesis methods
4-[(2,3,4-Tri-O-acetyl-6-deoxy-α-L-mannopyranosyl)oxy]benzaldehyde

88086-87-7
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4-Hydroxybenzaldehyde rhamnoside

88086-86-6
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Yield:88086-86-6 75%

Reaction Conditions:

with methanol;sodium methylate for 3 h;Ambient temperature;

References:

Leuck, Michael;Kunz, Horst [Carbohydrate Research,1998,vol. 312,# 1-2,p. 33 - 44]

Benzaldehyde, 4-[[6-deoxy-2,3,4-tris-O-(triethylsilyl)-α-L-mannopyranosyl]oxy]-

172163-97-2
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4-Hydroxybenzaldehyde rhamnoside

88086-86-6
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References
Rhaminopyranose, L-

73-34-7
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4-Hydroxybenzaldehyde rhamnoside

88086-86-6
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108740-74-5 Synthesis
Phenyl 2,3,4-Tri-O-acetyl-1-thio-α-L-rhamnopyranoside

108740-74-5
22 suppliers
$90.00/100mg

4-Hydroxybenzaldehyde rhamnoside

88086-86-6
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References
[(2S,3S,4R,5R)-4,5-Diacetyloxy-2-methyl-6-(2,2,2-trichloroethanimidoyl)oxyoxan-3-yl] acetate

122089-71-8
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4-Hydroxybenzaldehyde rhamnoside

88086-86-6
14 suppliers
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References