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
Crossref Cited-by Linking
- Baer Hans H., Hanna Hanna R.: Desulfonyloxylations of some secondary p-toluenesulfonates of glycosides by lithium triethylborohydride; a high-yielding route to 2- and 3-deoxy sugars. Carbohydrate Research 1982, 110, 19. <https://doi.org/10.1016/0008-6215(82)85023-4>
- 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. Chemistry Letters 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>
- Suami Tetsuo, Ogawa Seiichiro, Funaki Yuji: Inositol Derivatives. 9. Lithium Aluminum Hydride Reduction of Inositol Epoxides and Their Sulfonates. Bulletin of the Chemical Society of Japan 1975, 48, 1545. <https://doi.org/10.1246/bcsj.48.1545>
- 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. <https://doi.org/10.1002/chin.197136232>
