✦ LIBER ✦

Synthesis and Biological Evaluation of Tetrahydroisoquinolin-4-ol Derivatives

✍ Scribed by Williams, LR; Quessy, SN

Book ID: 111975628
Publisher: Commonwealth Scientific and Industrial Research Organisation Publishing
Year: 1979
Tongue: English
Weight: 562 KB
Volume: 32
Category: Article
ISSN: 0004-9425
DOI: 10.1071/ch9791317

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and biological evaluation of n

Synthesis and biological evaluation of novel piperidin-4-ol derivatives

✍ Zhiyong Weng; Wei Wei; Xiaowu Dong; Yongzhou Hu; Shufang Huang; Tao Liu; Xin Xie 📂 Article 📅 2011 🏛 Springer Vienna 🌐 English ⚖ 355 KB

ChemInform Abstract: Synthesis and Biolo

ChemInform Abstract: Synthesis and Biological Evaluation of Novel Piperidin-4-ol Derivatives.

✍ Zhiyong Weng; Wei Wei; Xiaowu Dong; Yongzhou Hu; Shufang Huang; Tao Liu; Xin Xie 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 31 KB

Synthesis and Biological Evaluation of P

Synthesis and Biological Evaluation of Pyridooxazine—Tetrahydroisoquinoline Derivatives as MDR Modulators.

✍ Chen Ma; Shao-Jie Liu; Liang Xin; Qun Zhang; Kai Ding; J. R. Falck; Dong-Soo Shi 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

Synthesis and biological evaluation of f

Synthesis and biological evaluation of fragmented derivatives of tetrahydroisoquinolines. 3. Trimetoquinol studies

✍ Miller, Duane D.; Kador, Peter F.; Venkatraman, R.; Feller, Dennis R. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 507 KB

Synthesis and biological evaluation of f

Synthesis and biological evaluation of fragmented derivatives of tetrahydroisoquinolines. 2. Trimetoquinol studies

✍ Miller, Duane D.; Osei-Gyimah, Peter; Bardin, John; Feller, Dennis R. 📂 Article 📅 1975 🏛 American Chemical Society 🌐 English ⚖ 524 KB

Diastereoselective synthesis and optical

Diastereoselective synthesis and optical resolution of 3,4-substituted tetrahydroisoquinolin-4-ols

✍ Masaru Kihara; Motoki Ikeuchi; Kaori Jinno; Minoru Kashimoto; Yoshimaro Kobayash 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 493 KB

mixture was poured into ice-water(l00 ml) and extracted with CHC13(100 ml x 3). The extract was washed with H20, dried over MgS04 and evaporated to give Z-methylpropyl phenyl ketone(5d) as an oil(l6.20 g, 94%). 'H-NMR: 8.00(2H,dd,J=8.5 and 1.5Hz1, 7.60-7.23 (3H,m), 2.84(2H,d, J=6.8Hz), 2.40-2.08(lH,