171714. lajstromszámú szabadalom • Fungicid szerek, valamint eljárás a hatóanyagként alkalmazható azolitérek fémkomplexeinek előállítására
7 171714 8 x a n Y B R X a n Y B R 4—O—CO—fenil 1 1 CH CO C(CH3 ) 3 4—N0 2 1 0 N CHOH C(CH3 ) 3 4—NH—COCH 8 1 1 CH CO C(CH3 ) 3 4—C(CH 3) 3 1 0 N CHOH C(CH3 ) 3 4—OCH 3 1 1 CH CO C(CH3 ) 3 5 4-CH3 1 0 N CHOH C(CH3 ) 3 3-N02 1 1 CH CO C(CH3 ) 3 2—CI 1 0 N CHOH C(CH3 ) 3 3—CN 1 1 CH CO C(CH3 ) 3 3—CI 1 0 N CHOH C(CH3 ) 3 3—Br 1 1 CH CO C(CH3 ) 3 — 0 0 N CHOH C(CH3 ) 3 3—F 1 1 CH CO C(CH3 ) 3 4—CI 1 0 N CHOH C(CH3 ) 3 3—OCH3 1 1 CH CO C(CH3 ) 3 10 4—CI 1 0 N CHOH CH3 3-CHj 1 1 CH CO C(CH3 ) 3 4—CI 1 0 N CHOH —fenil 3-N(CH3 ) 2 1 1 CH CO C(CH3 ) 3 4—Br 1 0 N CHOH C(CH3 ) 3 3—O—CO—CH B 1 1 CH CO C(CH3 ) 3 4—F 1 0 N CHOH C(CH3 ) 3 3—O—CO—fenií 1 1 CH CO C(CH3 ) 3 4—fenil 1 0 N CHOH C(CH3 ) 3 3—N0 2 1 1 CH CO C(CH3 ) 3 15 2—fenil 1 0 N CHOH C(CH3 ) 3 2—CN 1 1 CH CO C(CH3 ) 3 2,4—CI 2 0 N CHOH C(CH3 ) 3 2—O—CO—CH 3 1 1 CH CO C(CH3 ) 3 2—CH 3, 4—CI 2 0 N CHOH C(CH3 ) 3 2-CH3 1 1 CH CO C(CH3 ) 3 3,4—CH 3 2 0 N CHOH C(CH3 ) 3 2—0—CO—fenil 1 1 CH CO C(CH3 ) 3 2,4,5—CI 3 0 N CHOH C(CH3 ) 3 2—F 1 1 CH CO C(CH3 ) 3 20 4—CO—O—CH 8 1 0 N CHOH C(CH3 ) 3 2—CO—fenil 1 1 CH CO C(CH3 ) 3 4—fenil, 2,6—CI 3 0 N CHOH C(CH3 ) 3 2—0—fenil 1 1 CH CO C(CH3 ) 3 2—CI, 4—fenil 2 0 N CHOH C(CH3 ) 3 3—CI 1 0 CH CHOH C(CH3 ) 3 4—CI—fenil 1 0 N CHOH C(CH3 ) 3 4—CI 1 0 CH CHOH C(CH3 ) 3 2—ciklohexil 1 0 N CHOH C(CH3 ) 3 4—Br 1 0 CH CHOH C(CH3 ) 3 25 4—ciklohexil 1 0 N CHOH C(CH3 ) 3 4—F 1 0 CH CHOH C(CH3 ) 3 2,4,6—CI 3 0 N CHOH C(CH3 ) 3 2,4—CI 2 0 CH CHOH C(CH3 ) 3 4—J 1 0 N CHOH C(CH3 ) 3 2,6—CI 2 0 CH CHOH C(CH3 ) 3 4—S0 2—CH 3 1 0 N CHOH C(CH3 ) 3 2—fenil 1 0 CH CHOH C(CH3 ) 3 4—CN 1 0 N CHOH C(CH3 ) 3 4—fenil 1 0 CH CHOH C(CG3 ) 3 30 4—S0 2—fenil 1 0 N CHOH C(CH3 ) 3 4-C(CH3 ) 8 1 0 CH CHOH C(CH3 ) 3 4—CO—fenil 1 0 N CHOH C(CH3 ) 3 2—CI, 4—fenil 2 0 CH CHOH C(CH3 ) 3 4—O—S0 2—CH .1 0 N CHOH C(CH3 ) 3 2,6—CI, 4—fenil 3 0 CH CHOH C(CH3 ) 3 4—OCF 3 1 0 N CHOH C(CH3 ) 3 — 0 0 CH CHOH C(CH3 ) 3 4—O—CO—CH a , 1 0 N CHOH C(CH3 ) 3 4—ciklohexil 1 0 CH CHOH C(CH3 ) 3 35 4—0—CO—fenil 1 0 N CHOH C(CH3 ) 3 2—ciklohexil 1 0 CH CHOH C(CH3 ) 3 4—NH—COCH 3 1 0 N CHOH C(CH3 ) 3 4—CI—fenil 1 0 CH CHOH C(CH3 ) 3 4—OCH 3 1 0 N CHOH C(CH3 ) 3 4—J 1 0 CH CHOH C(CH3 ) 3 3—N0 2 1 0 N CHOH C(CH3 ) 3 4—S0 2—CHg 1 0 CH CHOH C(CH3 ) 3 3—CN 1 0 N CHOH C(CH3 ) 3 4—S0 2—fenil 1 0 CH CHOH C(CH3 ) 3 40 3—Br 1 0 N CHOH C(CH3 ) 3 4—CN 1 0 CH CHOH C(CH3 ) 3 3—F 1 0 N CHOH C(CH3 ) 3 4—CO—fenil 1 0 CH CHOH C(CH3 ) 3 3—OCH 3 1 0 N CHOH C(CH3 ) 3 4—O—S0 2—CH, jl 0 CH CHOH C(CH3 ) 3 3-CH3 1 0 N CHOH C(CH3 ) 3 4—OCF 3 1 0 CH CHOH C(CH3 ) 3 3—N(CH 3) 2 1 0 N CHOH C(CH3 ) 3 4—O—CO—CH 8 1 0 CH CHOH C(CH3 )3 45 3—O—CO—CHj 1 1 0 N CHOH C(CH3 ) 3 4—0—CO—fenil 1 0 CH CHOH C(CH3 ) 3 3—0—CO—fenil 1 0 N CHOH C(CH3 ) 3 4—NH—COCH B 1 0 CH CHOH C(CH3 ) 3 2—N0 2 1 0 N CHOH C(CH3 ) 3 4—OCH 3 1 0 CH CHOH C(CH3 ) 3 2—CN 1 0 N CHOH C(CH3 ) 3 3—N0 2 1 0 CH CHOH C(CH3 ) 3 2—O—CO—CH, 1 1 0 N CHOH C(CH3 ) 3 3—CN 1 0 CH CHOH C(CH3 ) 3 50 2-CH3 1 0 N CHOH C(CH3 ) 3 3—Br 1 0 CH CHOH C(CH3 ) 3 2—0—CO—fenil 1 1 0 N CHOH C(CH3 ) 3 3—F 1 0 CH CHOH C(CH3 ) 3 2—F 1 0 N CHOH C(CH3 ) 3 3—OCH 3 1 0 CH CHOH C(CH3 ) 3 2—CO—fenil 1 0 N CHOH C(CH3 ) 3 3-CH3 1 0 CH CHOH C(CH3 ) 3 2—0—fenil 1 0 N . CHOH C(CH3 ) 3 3—N(CH 3) 2 1 0 CH CHOH C(CH3 ) 3 55 2—CH 3, 4—CI 1 0 N CHOH C(CH3 ) 3 3—O—CO—CH a 1 1 0 CH CHOH C(CH3 ) 3 4—CI 2 1 N CHOH C(CH3 ) 3 3—0—CO—fenil I 1 0 CH CHOH C(CH3 ) 3 2—CI 1 1 N CHOH C(CH3 ) 3 2—N0 2 1 0 CH CHOH C(CH3 ) 3 3—CI 1 1 N CHOH C(CH3 ) 3 2—CN 1 0 CH CHOH C(CH3 ) 3 2,4—CI 2 1 N CHOH C(CH3 ) 3 2—O—CO—CH, • 1 0 CH CHOH C(CH3 ) 3 60 2,5—CI 2 1 N CHOH C(CH3 ) 3 2-CH3 1 0 CH CHOH C(CH3 ) 3 2,3—CH 3 2 1 N CHOH C(CH3 ) 3 2—0—CO—fenil I 1 0 CH CHOH C(CH3 ) 3 4—F 1 1 N CHOH C(CH3 ) 3 2—F 1 0 CH CHOH C(CH3 ) 3 — 0 1 N CHOH C(CH3 ) 3 2—CO—fenil 1 0 CH CHOH C(CH3 ) 3 2,4—CI 2 1 N CHOH —fenil—CI 2—0—fenil 4 1 0 CH CHOH C(CH3 ) 3 65 0 1 N CHOH —fenil
