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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
ChemicalBook CAS DataBase List METHYL ALPHA-L-RHAMNOPYRANOSIDE
15814-59-2

METHYL ALPHA-L-RHAMNOPYRANOSIDE synthesis

8synthesis methods
α-D-Mannopyranoside, methyl 6-deoxy-6-iodo-

52290-43-4
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METHYL ALPHA-L-RHAMNOPYRANOSIDE

15814-59-2
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-

Yield:15814-59-2 100%

Reaction Conditions:

with 20% palladium hydroxide-activated charcoal;hydrogen;N-ethyl-N,N-diisopropylamine in methanol; for 0.5 h;

References:

Kaufmann, Elias;Hattori, Hiromu;Miyatake-Ondozabal, Hideki;Gademann, Karl [Organic Letters,2015,vol. 17,# 14,p. 3514 - 3517] Location in patent:supporting information

α-D-Mannopyranoside, methyl 6-deoxy-, tribenzoate (9CI)

7512-03-0
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METHYL ALPHA-L-RHAMNOPYRANOSIDE

15814-59-2
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References
617-04-9 Synthesis
METHYL-ALPHA-D-MANNOPYRANOSIDE

617-04-9
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METHYL ALPHA-L-RHAMNOPYRANOSIDE

15814-59-2
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References
α-D-Mannopyranoside, methyl 3,4-O-[(1S,2S)-1,2-dimethoxy-1,2-dimethyl-1,2-ethanediyl]-

176897-12-4
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METHYL ALPHA-L-RHAMNOPYRANOSIDE

15814-59-2
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References
α-D-Mannopyranoside, methyl 6-bromo-6-deoxy-, triacetate (9CI)

30589-67-4
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METHYL ALPHA-L-RHAMNOPYRANOSIDE

15814-59-2
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References

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