✦ LIBER ✦

The synthesis of 1,5-dideoxy-1,5-(alkyl)imino-2-C-methyl-d-glucitols

✍ Scribed by Ish K. Khanna; Richard M. Weier; Janet Julien; Richard A. Mueller; David C. Lankin; Lydia Swenton

Publisher: Elsevier Science
Year: 1996
Tongue: French
Weight: 250 KB
Volume: 37
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)00021-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of the antibiotic 1,5-dideoxy-

Synthesis of the antibiotic 1,5-dideoxy-1,5-imino-D-glucitol; concomitant formation of the D-mannitol analogue

✍ H. J. G. Broxterman; G. A. van der Marel; J. H. van Boom; J. J. Neefjes; H. L. P 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 691 KB

Synthesis of (+)-1,5-dideoxy-1,5-imino-d

Synthesis of (+)-1,5-dideoxy-1,5-imino-d-galactitol, a potent α-d-galactosidase inhibitor

✍ Ronald C. Bernotas; Michael A. Pezzone; Bruce Ganem 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 459 KB

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of 1,4-Dideoxy-1,4-imino-L-lyxitol and 1,5-Dideoxy-1,5-imino-D-ribitol.

✍ Ki Chang Jang; Ill-Yun Jeong; Min Suk Yang; Sang Uk Choi; Ki Hun Park 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

ChemInform Abstract: Total Syntheses of

ChemInform Abstract: Total Syntheses of (+)- and (-)-1-Deoxynojirimycin (1,5-Dideoxy-1,5-imino-D- and L-glucitol) and of (+)- and (-)-1-Deoxyidonojirimycin (1,5-Dideoxy-1,5-imino-D- and L-iditol) via Furoisoxazoline-3-aldehydes.

✍ Christophe Schaller; Pierre Vogel; Volker Jaeger 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Preparation of theN-Acetylglucosaminidas

Preparation of theN-Acetylglucosaminidase Inhibitor 1-Acetamido-1,2,5-trideoxy-2,5-imino-D-glucitol from Methyl α-D-Mannopyranoside

✍ Schumacher-Wandersleb, Michael H. M. G. ;Petersen, Stefan ;Peter, Martin G. 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 740 KB

## Abstract Fragmentation of methyl 3‐__O__‐benzyl‐6‐bromo‐2‐__O__‐(__tert__‐butyldimethylsilyl)‐6‐deoxy‐4‐__O__‐(4‐methoxybenzyl)‐α‐D‐mannopyranoside (2) and in situ reductive amination give (3__R__,4__S__,5__R__)‐6‐benzylamino‐4‐benzyloxy‐5‐(__tert__‐butyldimethylsilyloxy)‐3‐(4‐methoxybenzyloxy)h

Synthesis of 1,5-dideoxy-1,5-imino-d-xyl

Synthesis of 1,5-dideoxy-1,5-imino-d-xylonolactam VIA acid-catalyzed intramolecular schmidt rearrangement

✍ Peter Norris; Derek Horton; Brett R. Levine 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 225 KB