化学
异丙基
核磁共振波谱
二维核磁共振波谱
光谱学
碳-13核磁共振
核磁共振谱数据库
立体化学
药物化学
谱线
天文
量子力学
物理
作者
Todd M. Alam,Ming‐Eng Liu,Daryl K. Garcia,Valerie M. Hernandez,Richard R. Malone,Brian B. Chamblee,Lorraine M. Deck,Robert E. Royer
标识
DOI:10.1002/mrc.1260330717
摘要
Abstract 1 H and 13 C NMR studies were carried out on the substituted dihydronaphthalene compounds 1,2‐dihydro‐8‐isopropyl‐6,7‐dimethoxy‐2‐methylnaphthalene, 3‐bromo‐1, 2‐dihydro‐8‐isopropyl‐6, 7‐dimethoxy‐2‐methylnaphthalene, 3, 4‐dihydro‐5‐isopropyl‐6, 7‐dimethoxy‐3‐methyl‐1(2 H )‐naphthalenone, 1, 2‐dihydro‐6, 7‐dimethoxy‐2, 8‐dimethylnaphthalene, 3‐bromo‐1, 2‐dihydro‐6, 7‐dimethoxy‐2, 8‐dimethylnaphthalene and 3, 4‐dihydro‐6, 7‐dimethoxy‐3, 5‐dimethyl‐1(2 H )‐naphthalenone. Complete assignments of the proton and carbon spectra were made using one‐ and two‐dimensional NMR techniques including APT, COSY, NOESY and 1 H‐ 13 C HETCOR spectroscopy.
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