Iodocyclization of 1,4-dihydropyridines

被引：17

作者：

Lavilla, R ^{[1
]}

Coll, O ^{[1
]}

Nicolàs, M ^{[1
]}

Bosch, J ^{[1
]}

机构：

[1] Univ Barcelona, Fac Pharm, Organ Chem Lab, E-08028 Barcelona, Spain

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 28期

关键词：

cyclization; halogenation; pyridines; oxazolidines;

D O I：

10.1016/S0040-4039(98)00912-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Iodine (or related species) addition to 1,4-dihydropyridinls, with properly attached substituents at the nitrogen atom, leads to the corresponding 3-iodotetrahydlopyridinium ions, which undergo an internal nucleophilic attack to furnish regio- and stereoselectively iodobi(poly)heterocyclic ring systems in good yields. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：5089 / 5092

页数：4

共 50 条

[1] PHOTOOXIDATION OF 1,4-DIHYDROPYRIDINES
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[2] OXIDATION OF 1,4-DIHYDROPYRIDINES
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[3] REACTIONS OF 1,4-DIHYDROPYRIDINES
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[4] REACTIONS OF 1,4-DIHYDROPYRIDINES
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[5] THE ALKYLATION OF HANTZSCH 1,4-DIHYDROPYRIDINES
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[8] PREPARATION OF NEW 1,4-DIHYDROPYRIDINES
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[9] REARRANGEMENTS OF 1,4-DIHYDROPYRIDINES INTO PYRROLES
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