✦ LIBER ✦

Benzene-di-N-Substituted Carbamates as Conformationally Constrained Substrate Analogs of Cholesterol Esterase

✍ Scribed by S.-Y. Chiou; M.-C. Lin; M.-T. Hwang; H.-G. Chang; G. Lin

Book ID: 106423823
Publisher: Springer
Year: 2008
Tongue: English
Weight: 359 KB
Volume: 27
Category: Article
ISSN: 1573-4943
DOI: 10.1007/s10930-008-9135-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Benzene-di-N-substituted carbamates as c

Benzene-di-N-substituted carbamates as conformationally constrained analogs of Pseudomonas lipase substrates

✍ Ming-Cheng Lin; Mei-Ting Hwang; Han-Ging Chang; Chung-Sheng Lin; Gialih Lin 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 294 KB

Benzene-1,2-, 1,3-, and 1,4-di-N-substit

Benzene-1,2-, 1,3-, and 1,4-di-N-substituted carbamates as conformationally constrained inhibitors of acetylcholinesterase

✍ Ming-Cheng Lin; Mei-Ting Hwang; Han-Ging Chang; Chung-Sheng Lin; Gialih Lin 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 214 KB

## Abstract Benzene‐1,2‐, 1,3‐, and 1,4‐di‐__N__‐substituted carbamates (1–15) are synthesized as the conformationally constrained inhibitors of acetylcholinesterase and mimic __gauche__, __eclipsed__, and __anti__‐conformations of acetylcholine, respectively. All carbamates 1–15 are characterized