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Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates

✍ Scribed by Aguilera, Begoña; Fernández-Mayoralas, Alfonso

Book ID
125483286
Publisher
American Chemical Society
Year
1998
Tongue
English
Weight
88 KB
Volume
63
Category
Article
ISSN
0022-3263

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📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of a Thio
ChemInform Abstract: Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates.
✍ B. AGUILERA; A. FERNANDEZ-MAYORALAS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

Synthesis of a Thio-Analogue of Lewis X by Regioselective Opening of Cyclic Sulfamidates. -The synthesis of the title analogue (I) contains linking of galactose and allosamine, protected by a p-methoxyphenyl group at O-6 (higher yield), transformation into cyclic sulfamidate, and its regioselective

ChemInform Abstract: Synthesis of Thio-L
ChemInform Abstract: Synthesis of Thio-Linked Analogues of Lewis X and Sialyl Lewis X.
✍ T. EISELE; R. R. SCHMIDT 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A short synthesis of chiral peraza-macro
A short synthesis of chiral peraza-macrocycles through opening of cyclic sulfamidates
✍ B.Moon Kim; Soon Mog So 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 270 KB

Efficient and general synthetic methods for novel chiral peraza-macrocycles have been developed. Sequential reactions of the known cyclic sulfamidate 4 derived from N-benzyl-L-serine methyl ester with pmethoxybenzylamine provided a symmetric triamine 3, which served as a building block for the const