Alternative formal synthesis of the potent D1 dopamine agonist dihydroxy-2,3,7,11b-tetrahydro-1H-naphth[1,2,3-de]isoquinoline:: Dinapsoline

被引：10

作者：

Qandil, AM ^{[1
]}

Ghosh, D ^{[1
]}

Nichols, DE ^{[1
]}

机构：

[1] Purdue Univ, Sch Pharm & Pharmacal Sci, Dept Med Chem & Mol Pharmacol, W Lafayette, IN 47907 USA

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1999年 / 64卷 / 04期

关键词：

D O I：

10.1021/jo982067z

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：1407 / 1409

页数：3

共 8 条

[1] 8,9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: A potent full dopamine D-1 agonist containing a rigid beta-phenyldopamine pharmacophore [J].

Ghosh, D ;

Snyder, SE ;

Watts, VJ ;

Mailman, RB ;

Nichols, DE .

JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (02) :549-555

[2] ONE-STEP SYNTHESIS OF PHTHALIDYLISOQUINOLINE ALKALOIDS, CORDRASTINE AND HYDRASTINE [J].

KAMETANI, T ;

HONDA, T ;

INOUE, H ;

FUKUMOTO, K .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1976, (11) :1221-1225

[3] STUDIES IN PROSTAGLANDINS .10. SYNTHESIS OF PROSTAGLANDIN MODELS AND PROSTAGLANDINS BY CONJUGATE ADDITION OF A FUNCTIONALIZED ORGANOCOPPER REAGENT [J].

KLUGE, AF ;

UNTCH, KG ;

FRIED, JH .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (22) :7827-&

[4]

KUNITOMO J, 1985, CHEM PHARM BULL, V33, P5245

[5] AN EFFICIENT SYNTHESIS OF 4-ARYL-1,2,3,4-TETRAHYDROISOQUINOLINES [J].

MILLER, RB ;

SVOBODA, JJ .

SYNTHETIC COMMUNICATIONS, 1994, 24 (08) :1187-1193

[6] PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS OF ORGANOBORON COMPOUNDS [J].

MIYAURA, N ;

SUZUKI, A .

CHEMICAL REVIEWS, 1995, 95 (07) :2457-2483

[7] PALLADIUM-CATALYZED CROSS-COUPLING OF PHENYLBORONIC ACID WITH HETEROCYCLIC AROMATIC HALIDES [J].

STAVENUITER, J ;

HAMZINK, M ;

VANDERHULST, R ;

ZOMER, G ;

WESTRA, G ;

KRIEK, E .

HETEROCYCLES, 1987, 26 (10) :2711-2716

[8]

WUSTROW DJ, 1991, SYNTHESIS-STUTTGART, P993

← 1 →