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Table 22.2 Selected fluorous precursors, intermediates and ligands
Precursor (educt)
Product [Ref.]
R f n -I [36]
Ar-R f n [37]
Het-R f n [37]
Ar-R f n [33, 3 8 , 39]
R f n R 2 C 6 H 2 OH, (R f n R 2 C 6 H 2 O) 3 P [40]
p -R f n C 6 H 4 OH, ( p -R f n C 6 H 4 O) 3 P [41]
p -R f n C 6 H 4 Br, ( p -R f n C 6 H 4 ) 3 P [41]
2,4-(R f n ) 2 ArOH, [2,4-(R f n ) 2 ArO] 3 P [42]
[R f n CH = CH-(CH 2 ) m ] 2 -bipy [43]
ArS-R f n , AlkS-R f n [33]
2,4-(R f 8 )C 6 H 3 SeC 4 H 9 [44]
R f n CH 2 CH 2 I [45]
[R f n CH 2 CHISi(CH 3 ) 3 , R f n CH = CH 2 [46]
R f n CH 2 CH(I)CH 2 OH [47]
R f n CH 2 CH 2 CH 2 OH, n = 6 [47]
n = 8 [4 8 ]; n = 6, 8 , 10 [49]
R f n CH 2 CH 2 (CH 2 ) m OH, n = 8 , m = 1, 2, 3 [50]
R f n CH 2 CHIOAc, R f n CH 2 CH = O [51]
R f n -Br
R f n -S-R, R = alkyl, aryl [52]
R f n -Cl
R f n CH 2 CH 2 R, R = alkyl, CH 2 Si(CH 3 ) 3 [53]
R f n CH 2 CH 2 R, R f n SO 2 Cl [54]
R f n -CO 2 H
R f7 C(O)CH 2 C(O)R f7 [55]
R f n CH 2 CH 2 I
R f n CH = CH 2 [56]
(Ferrocene)(CH 2 CH 2 R f n ) 2 [57]
(R f n CH 2 CH 2 ) 2 P(( - )menthyl) [5 8 ]
(R f n C 6 H 4 ) 2 PCH 2 CH 2 P(C 6 H 4 R f n ) 2 [41]
( m -R f n CH 2 CH 2 C 6 H 4 ) 3 P [59]
[(R f n CH 2 CH 2 C 6 H 4 ) 2 PCH 2 -] 2 [59]
[(R f n CH 2 CH 2 ) 2 P(BH 3 )CH 2 -] 2 [60]
(R f n CH 2 CH 2 ) 3 - n SiMe n Cl, n = 0, 1, 2 [35]
[(R f n CH 2 CH 2 ) 3 - n SiMe n C 6 H 4 ] 3 P, n = 0, 1, 2 [35]
(R f n CH 2 CH 2 ) 3 SiBr [61]
(R f n CH 2 CH 2 ) 3 SnR, R = Ph, Br, H [62]
[(R f6 CH 2 CH 2 ) 2 SnO] n [63]
R f 8 CH 2 CH 2 OC(O)CH = CH 2 -
- [(Ph 2 PC 6 H 4 )CHCH 2 ) 1 - [CH(CO 2 CH 2 CH 2 R f 8 )CH 2 ] n - , fluorous polymer-supported
arylphosphine [64]
[R f n CH 2 CH 2 P(C 6 H 5 ) 3 ] + I -
Ar(CH = CHCH 2 R f n ) x , Ar(CH 2 CH 2 CH 2 R f n ) x [65]
R f 8 (CH 2 ) m I, m = 2-4
R f 8 (CH 2 ) m PH 2 , m = 2-4; R f 8 (CH 2 ) m P[(CH 2 ) m ¢ R f 8 ] 2 , m / m ¢= 3/2, 2/3, 4/3, 3/4 [66]
R f n CH 2 CH 2 CH 2 I
(R f n CH 2 CH 2 CH 2 OAr) 3 P(O) x , x = 0, 1[67]
[ - N(CH 2 CH 2 CH 2 R f n )CH 2 CH 2 - ] 3 [4 8 ]
(R f 8 CH 2 CH 2 CH 2 ) 2 NCH 3 [13]
[R f7 CH 2 CH 2 CH 2 CH 2 ] 2 bipy [6 8 ]
R f n CH 2 CH 2 CH 2 OTs
N(CH 2 CH 2 N(CH 2 CH 2 CH 2 R f6 ) 2 ) 3 [69]
R f7 CH 2 OH
[R f7 CH 2 OCH 2 ] 2 bipy [6 8 ]
R f n (CH 2 ) n OH
R f n (CH 2 ) n OP(O)[N(CH 2 CH 2 ) 2 O] 2 , n = 1, 3 [70]
R f n CH 2 OSO 2 C 4 F 9
(R f n CH 2 OAr) 3 P(O) x , x = 0, 1 [67]
R f n CH 2 CH 2 OH
(R f n CH 2 CH 2 O) 3 P [9]
 
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