Abstract
Under Minisci reaction conditions, nucleophilic carbon free radicals readily substitute ferrocene (as the ferricinium ion) and protonated acetophenone, the latter reaction being highly positionally specific.
| Original language | English |
|---|---|
| Pages (from-to) | 4783-4786 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 20 |
| Issue number | 49 |
| DOIs | |
| Publication status | Published - 1979 |
| Externally published | Yes |
Fingerprint
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Nucleophilic reactions in strongly acidic media. Highly specific homolytic aromatic alkylation and acylation. / Bin Din, Laily; Meth-Cohn, Otto; Walshe, Nigel D A.
In: Tetrahedron Letters, Vol. 20, No. 49, 1979, p. 4783-4786.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Nucleophilic reactions in strongly acidic media. Highly specific homolytic aromatic alkylation and acylation
AU - Bin Din, Laily
AU - Meth-Cohn, Otto
AU - Walshe, Nigel D A
PY - 1979
Y1 - 1979
N2 - Under Minisci reaction conditions, nucleophilic carbon free radicals readily substitute ferrocene (as the ferricinium ion) and protonated acetophenone, the latter reaction being highly positionally specific.
AB - Under Minisci reaction conditions, nucleophilic carbon free radicals readily substitute ferrocene (as the ferricinium ion) and protonated acetophenone, the latter reaction being highly positionally specific.
UR - http://www.scopus.com/inward/record.url?scp=0039869799&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0039869799&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(01)86710-1
DO - 10.1016/S0040-4039(01)86710-1
M3 - Article
AN - SCOPUS:0039869799
VL - 20
SP - 4783
EP - 4786
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 49
ER -