CYCLO-ADDITION REACTION WITH METHYLNITRONE

被引：28

作者：

FORNEFELD, EJ

PIKE, AJ

机构：

[1] The Lilly Research Laboratories, Indiana 46206, Indianapolis

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 05期

关键词：

D O I：

10.1021/jo01319a038

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Cycloaddition of in situ prepared methylnitrone proceeds in good yields with active dipolarophiles. The resultant isoxazolidines were converted to various transformation products. A convenient synthesis of α-acylstyrenes is described. © 1979, American Chemical Society. All rights reserved.

引用

页码：835 / 839

页数：5

共 13 条

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[2] BROWN CW, 1960, P CHEM SOC LONDON, P254
[3] BROWN CW, 1960, Patent No. 850418
[4] CAVELLA J, 1961, Patent No. 862513
[5] NITRONES
HAMER, J
MACALUSO, A
[J]. CHEMICAL REVIEWS, 1964, 64 (04) : 473 - +
[6] HUISGEN R, 1968, TETRAHEDRON LETT, P2559
[7] HUISGEN R, 1960, TETRAHEDRON LETT, P9
[8] HUISGEN R, 1968, TETRAHEDRON LETT, P2548
[9] HUISGEN R, 1968, TETRAHEDRON LETT, P2568
[10] KETENES .8. SOME REACTIONS OF 1-(DIMETHYLAMINO)-4-METHYL-1-PENTEN-3-1
MARTIN, JC
BARTON, KR
GOTT, PG
MEEN, RH
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1966, 31 (03) : 943 - &

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