STRUCTURAL REARRANGEMENT OF IPRODIONE IN ETHANOLIC SOLUTION

被引：15

作者：

COOKE, BK

LOEFFLER, RST

PAPPAS, AC

机构：

[1] University of Bristol, Long Ashton Research Station, Bristol

来源：

PESTICIDE SCIENCE | 1979年 / 10卷 / 05期

关键词：

D O I：

10.1002/ps.2780100505

中图分类号：

S3 [农学（农艺学）];

学科分类号：

0901 ;

摘要：

Iprodione, in ethanolic solution, was found to undergo structural rearrangement over a period of days to give a solid product which was shown by mass spectrometry to be an isomer. Mechanistic considerations led to a proposed structure, which was verified by synthesis of an authentic specimen by an unambiguous route. The biological implications of these findings are discussed. Copyright © 1979 John Wiley & Sons, Ltd

引用

页码：393 / 398

页数：6

共 6 条

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[2] Horne W. H., 1943, ORG SYNTH, V2, P453
[3] LEROUX P, 1977, PHYTOPATHOL Z, V89, P347
[4] The metamorphosis of α-amino acids in phenyl hydantoine
Mouneyrat, A
[J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1900, 33 : 2393 - 2396
[5] COMPARISON OF THE MECHANISMS OF ACTION OF VINCLOZOLIN, PROCYMIDONE, IPRODIONE AND PROCHLORAZ AGAINST BOTRYTIS-CINEREA
PAPPAS, AC
FISHER, DJ
[J]. PESTICIDE SCIENCE, 1979, 10 (03): : 239 - 246
[6] PHILAGRO SA, 1977, Patent No. 2640872

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