“…The reagent is able to selenate amides and formamides by substitution of the oxygen atom [40,41]. The condensation of dichlorphenylphosphine (7) with magnesium in THF [42][43][44][45][46] yields pentaphenylpentaphospholane [(PhP) 5 , (8)] SCHEME 1 (i) HCOOEt [38] (ii) COCl 2 [38] or ClCOOCCl 3 (diphosgene) (iii) Se, CHCl 3 [39] (iv) (5a-h) HX, benzene (6a,b) HX/NaX.…”
“…The reagent is able to selenate amides and formamides by substitution of the oxygen atom [40,41]. The condensation of dichlorphenylphosphine (7) with magnesium in THF [42][43][44][45][46] yields pentaphenylpentaphospholane [(PhP) 5 , (8)] SCHEME 1 (i) HCOOEt [38] (ii) COCl 2 [38] or ClCOOCCl 3 (diphosgene) (iii) Se, CHCl 3 [39] (iv) (5a-h) HX, benzene (6a,b) HX/NaX.…”
“…The formation of the side-product 11 was observed. The structure of 11 was attributed by means of its spectral data, especially by the A 2 B nature of its 31 P{ 1 H} NMR spectrum ( [27,28].…”
“….93 a [9,10] 7.92 b [11] 8.02 c [25] 7.95 d [25] 10.10 a [9,10] 11.08 b [11] 9.21 d [15] 9.21 d [16] 10.56 d [17] 10.62 d [18] 10.32 d [19] 7.40 d [20] b 8.48 [21] 8.53 c [25] 8.48 d [25] 9.51 a [9] 9.36 / 9.46 b [14] 9.64 e [12] 11.17 d [18] 11.22 d [22] 8.10 d [13] c 8.55 d [23] 8.64 d [24] 7.60 d , f 10.0 d [16] 8.67 d [20] 11.75 d [16] 8.18 d [25] …”
The reaction of N, N-diaryl-substituted formamides with oxalyl chloride gives rise, instead to the formation of the expected salt-like formamide chlorides, to the formation of corresponding non-ionic N-dichloromethyl-substituted diarylamines.
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