Collect. Czech. Chem. Commun.
1971, 36, 1860-1866
https://doi.org/10.1135/cccc19711860
Reduction of secondary p-toluenesulfonyloxy groups with lithium aluminum hydride in sugar series. III. Reduction of methyl 4,6-O-benzylidene-2,3-di-O-p-toluenesulfonyl-α-D-idopyranoside and α-D-altropyranoside
A. Zobáčová, V. Heřmánková and J. Jarý
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- Mitsunobu Oyo, Kudo Takashi, Nishida Mitsuru, Tsuda Nobuo: A ONE-STEP PREPARATION OF 2,3-ANHYDRO-4,6-O-BENZYLIDENE-α-D-ALLOPYRANOSIDE AND -GULOPYRANOSIDE. Chem. Lett. 1980, 9, 1613. <https://doi.org/10.1246/cl.1980.1613>
- Hughes Neil A., Tyson Phillip D.: A convenient synthesis of 5,6-anhydro-1,2-O-isopropylidene-3-O-methanesulphonyl-β-l-idofuranose, and its conversion into 6-substituted l-idofuranose derivatives. Carbohydrate Research 1977, 57, 317. <https://doi.org/10.1016/S0008-6215(00)81940-0>
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- ZOBACOVA A., HERMANKOVA V., JARY J.: ChemInform Abstract: REDUKTION SEKUNDAERER P-TOLUOLSULFONYLOXY-GRUPPEN MIT LITHIUMALUMINIUMHYDRID IN DER ZUCKER-REIHE 3. MITT. RED. VON METHYL-4,6-O-BENZYLIDEN-2,3-DI-O-P-TOLUOLSULFONYL-ALPHA-D-ALTROPYRANOSID UND -ALPHA-D-IDOPYRANOSID. Chemischer Informationsdienst. Organische Chemie 1971, 2, no. <https://doi.org/10.1002/chin.197136232>