Abstract
Dilithiation of a trimethylene-bridged ferrocene with n-butyllithium and TMEDA selectively metalated the ring at the 2,2′- or the 3,3′-positions. The dilithio derivatives were converted to the dicarboxylic acid, the dibromo, and the diiodo derivatives.
| Original language | English |
|---|---|
| Pages (from-to) | 1226-1229 |
| Number of pages | 4 |
| Journal | Organometallics |
| Volume | 1 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - Jan 1 1982 |
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ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
Cite this
Bridged Ferrocenes. 9. Lithiation and Subsequent Reactions of 1,1′-Trimethyleneferrocene. / Hillman, Manny; Matyevich, Linda; Fujita, Etsuko; Jagwani, Uttam; McGowan, Jefferson.
In: Organometallics, Vol. 1, No. 9, 01.01.1982, p. 1226-1229.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Bridged Ferrocenes. 9. Lithiation and Subsequent Reactions of 1,1′-Trimethyleneferrocene
AU - Hillman, Manny
AU - Matyevich, Linda
AU - Fujita, Etsuko
AU - Jagwani, Uttam
AU - McGowan, Jefferson
PY - 1982/1/1
Y1 - 1982/1/1
N2 - Dilithiation of a trimethylene-bridged ferrocene with n-butyllithium and TMEDA selectively metalated the ring at the 2,2′- or the 3,3′-positions. The dilithio derivatives were converted to the dicarboxylic acid, the dibromo, and the diiodo derivatives.
AB - Dilithiation of a trimethylene-bridged ferrocene with n-butyllithium and TMEDA selectively metalated the ring at the 2,2′- or the 3,3′-positions. The dilithio derivatives were converted to the dicarboxylic acid, the dibromo, and the diiodo derivatives.
UR - http://www.scopus.com/inward/record.url?scp=6244246488&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=6244246488&partnerID=8YFLogxK
U2 - 10.1021/om00069a022
DO - 10.1021/om00069a022
M3 - Article
AN - SCOPUS:6244246488
VL - 1
SP - 1226
EP - 1229
JO - Organometallics
JF - Organometallics
SN - 0276-7333
IS - 9
ER -