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Zakharychev, V. V.; Golubtsova, M. D.; Kovalenko, L. V.

doi:10.1023/a:1013160902476

Cited by 2 publications

(2 citation statements)

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“…For background to strobilurin A and strobilurin analogs, see: Zhao et al (2007); Balbaa (2007); Li et al (2010); Zakharychev et al (1999Zakharychev et al ( , 2001). For bond-length data, see: Allen et al (1987).…”

Section: Related Literaturementioning

confidence: 99%

“…The strobilurins (Balbaa, 2007;Li et al, 2010;Zhao et al, 2007) are one of the most important classes of agricultural fungicides, with Strobilurin A as the lead compound, which inhibit electron transfer in mitochondria, disrupt metabolism and prevent growth of the target fungi. Reaction of 2-hydroxyimino-3-oxobutanoic acid esters with hydrazine hydrate can afford a product with a structure close to that of Strobilurin A (Zakharychev et al, 1999;Zakharychev et al, 2001).…”

Section: S1 Commentmentioning

confidence: 99%

See 1 more Smart Citation

Diethyl 2,2′-bis(hydroxyimino)-3,3′-(hydrazinediylidene)dibutanoate

Tong

et al. 2012

Acta Cryst E

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Key indicators: single-crystal X-ray study; T = 296 K; mean (C-C) = 0.002 Å; R factor = 0.039; wR factor = 0.110; data-to-parameter ratio = 13.4.Each molecule of the title compound, C 12 H 18 N 4 O 6 , is located on an inversion centre at the mid-point of the central N-N bond. The azo groups C N of the Schiff base group have an E conformation and the azo groups in the oxime C N-O groups have a Z conformation. O-HÁ Á ÁO hydrogen bonds link neighbouring molecules into infinite monolayers perpendicular to the a axis. Related literature

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