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ChemInform Abstract: A New Approach to C-Branched Monosaccharides by the Stereoselective Hydrodesulfurization of Methyl 4,6-O-Benzylidene-3-(bis(methylthio) methylene)-3-deoxy-α-D-erythro-hexopyranosid-2-ulose.

✍ Scribed by K. PESEKE; G. THIELE; M. MICHALIK

Book ID: 112023872
Publisher: John Wiley and Sons
Year: 2010
Weight: 37 KB
Volume: 26
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199550190

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📜 SIMILAR VOLUMES

A new approach toC-branched monosacchari

A new approach toC-branched monosaccharides by the stereoselective hydrodesulfurization of methyl 4,6-O-benzylidene-3-[bis(methylthio)-methylene]-3-deoxy-α-D-erythro-hexopyranosid-2-ulose

✍ Peseke, Klaus ;Thiele, Gabriela ;Michalik, Manfred 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 486 KB

## Abstract The stereoselective reduction of methyl 4,6‐__O__‐benzylidene‐3‐[bis(methylthio)methylene]‐3‐deoxy‐α‐D‐__erythro__‐hexopyranosid‐2‐ulose 1 with sodium tetrahydridoborate and tributyltin hydride, respectively, to (Z)‐configured 4 is described. The increased reactivity of 4 compared to 1

ChemInform Abstract: Dimerization by Het

ChemInform Abstract: Dimerization by Hetero Diels—Alder Reaction of Methyl 4,6-O-Benzylidene-3-deoxy-3-C-methylene-α-D-erythro-hexopyranosid- 2-ulose.

✍ J. XIE; S. CZERNECKI 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views