2017
DOI: 10.1080/10426507.2017.1284836
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and characterization of new tetraalkylaminophosphonium chlorides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
2

Relationship

1
1

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 19 publications
0
2
0
Order By: Relevance
“…A tentative mechanism [17] to account for this rearrangement leading to P − P(NMe 2 ) is shown in Scheme 2 [Ar=−C 6 H 4 (4‐NMe 2 ]. Upon initial formation of a tetralkylphosphonium salt A , [16b] we were able to observe the intermediate tertiary phosphine B by 31 P NMR spectroscopy [δ(P) −40 ppm] [16a,23] . Collapse of B , via P−C cleavage/PR 2 radical coupling reactions affords the speculated acyclic species C .…”
Section: Resultsmentioning
confidence: 97%
“…A tentative mechanism [17] to account for this rearrangement leading to P − P(NMe 2 ) is shown in Scheme 2 [Ar=−C 6 H 4 (4‐NMe 2 ]. Upon initial formation of a tetralkylphosphonium salt A , [16b] we were able to observe the intermediate tertiary phosphine B by 31 P NMR spectroscopy [δ(P) −40 ppm] [16a,23] . Collapse of B , via P−C cleavage/PR 2 radical coupling reactions affords the speculated acyclic species C .…”
Section: Resultsmentioning
confidence: 97%
“…Yield, % 89, [29] 90, [30,31] 93 [32,33] Me 92, [29] 95 [30,31] 92, [29] 93 [30,31] 85 [30,31] 87 [29][30][31] 90 [31] F 82, [29] 83 [30,31] 90 [30,31] 83 [30,31] 97 [30,31] 97 [30,31] 91 [30,31] F 3 C 83 [31] HO 71 [31] 76 [31] 86 [31] 92 [30,31] Entry Ar Yield, % 93 [29] 65 [29] 82 [29] 90, [29] 97 [30,31] CN 94 [30,31] CF 3 72 [29][30][31] 84, [31] 97 [34] 83 [29] 99 [35] 91…”
Section: Entry Armentioning
confidence: 99%