✦ LIBER ✦

Synthesis of glycosidic analogues of N-acetylneuramoyl-L-alanyl-D-isoglutamine

✍ Scribed by A. E. Zemyakov; V. Ya. Chirva

Publisher: Springer
Year: 1987
Tongue: English
Weight: 456 KB
Volume: 23
Category: Article
ISSN: 0009-3130
DOI: 10.1007/bf00598682

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of N-acetylmuramyl-L- [U−14C]a

Synthesis of N-acetylmuramyl-L- [U−14C]alanyl-D-isoglutamine

✍ Shoichi Kusumoto; Kazuhiro Ikenaka; Tetsuo Shiba 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 232 KB

Synthesis of the γ-octadecylamide of N-a

Synthesis of the γ-octadecylamide of N-acetylmuramoyl-L-alanyl-D-isoglutamine

✍ A. E. Zemlyakov; V. Ya. Chirva 📂 Article 📅 1988 🏛 Springer 🌐 English ⚖ 183 KB

Synthesis of N-acetyl-β-D-glucosaminyl-(

Synthesis of N-acetyl-β-D-glucosaminyl-(1-4)-N-acetylmuramyl- L -alanyl-D-isoglutamine

✍ Shoichi Kusumoto; Koji Yamamoto; Tetsuo Shiba 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 273 KB

Our synthetic studies on muramyl peptides have significantly elucidated the relationship between the immunoadjuvant activity and the chemical structure. 2)

Biological activity of anomeric pairs of

Biological activity of anomeric pairs of lipophilic glycosides ofN-acetylmuramyl-L-alanyl-D-isoglutamine

✍ O. V. Kalyuzhin; A. E. Zemlyakov; N. G. Kalina; E. L. Mulik; F. N. Kuzovlev; O. 📂 Article 📅 2008 🏛 Springer US 🌐 English ⚖ 324 KB

Synthesis of ω-amino- and ω-carboxyalkyl

Synthesis of ω-amino- and ω-carboxyalkylamides of N-acetylmuramoyl-L-alanyl-D-isoglutamine

✍ V. O. Kur'yanov; T. F. Zhelobetskaya; A. E. Zemlyakov; V. Ya. Chirva 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 357 KB

Synthesis of acyclic analogs ofN-acetylm

Synthesis of acyclic analogs ofN-acetylmuramyl-L-alanyl-D-isoglutamine (MDP)

✍ Danklmaier, Johann ;Hünig, Helmut 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 665 KB

## Abstract The syntheses of the acyclic MDP analogs 27–37 is described, the carbohydrate moiety of muramic acid being replaced by acyclic amino alcohol structures. Their preparation was accomplished by hydrolytic cleavage of the cyclic, disubstituted 3‐morpholinones 2–5 and protection of the free