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General Strategies for the Synthesis of the Major Classes of C -Aryl Glycosides

✍ Scribed by Kaelin, David E.; Lopez, Omar D.; Martin, Stephen F.

Book ID: 125454167
Publisher: American Chemical Society
Year: 2001
Tongue: English
Weight: 47 KB
Volume: 123
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja0108640

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📜 SIMILAR VOLUMES

ChemInform Abstract: General Strategies

ChemInform Abstract: General Strategies for the Synthesis of the Major Classes of C-Aryl Glycosides

✍ David E. Kaelin Jr.; Omar D. Lopez; Stephen F. Martin 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

A Strategy for the Synthesis of Anthraqu

A Strategy for the Synthesis of Anthraquinone-Based Aryl- C -glycosides

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General entries to C-aryl glycosides. Fo

General entries to C-aryl glycosides. Formal synthesis of galtamycinone

✍ Beth Apsel; John A Bender; Maya Escobar; David E Kaelin Jr.; Omar D Lopez; Steph 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 190 KB

Utilizing a general entry we had developed for the synthesis of C-aryl glycosides, we have prepared the juglone derivatives 18-20 as well as the juglone precursor 13. Because 19 had been previously converted in two steps by Suzuki into galtamycinone (1), its preparation constitutes a total synthesis

Umpolung Strategy for the Synthesis of 2

Umpolung Strategy for the Synthesis of 2-Deoxy-C-aryl Glycosides: A Serendipitous, Efficient Route for C-Furanoside Analogues.

✍ S. Vijayasaradhi; Indrapal Singh Aidhen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Umpolung Strategy for the Synthesis of 2

Umpolung Strategy for the Synthesis of 2-Deoxy- C -aryl Glycosides: A Serendipitous, Efficient Route for C -Furanoside Analogues †

✍ Vijayasaradhi, S.; Aidhen, Indrapal Singh 📂 Article 📅 2002 🏛 American Chemical Society 🌐 English ⚖ 58 KB

A General Method for the Synthesis of C-

A General Method for the Synthesis of C-Glycosides of Nojirimycin

✍ Fuchss, Thomas ;Streicher, Hansjörg ;Schmidt, Richard R. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 803 KB

## Abstract Methyl 2,3,4,6‐tetra‐__O__‐acetyl‐__N__‐(benzyloxycarbonyl)nojirimycin (3) can be readily transformed into the corresponding azaglycal 6 or fluoride 7, which are versatile glycosyl/piperidinosyl donors. Reaction of 7 with allyltrimethylsilane, propinyltrimethylsilane, trimethylsilyl cya