Abstract
The use of lithium butyl(phenylthio)cuprate as a reactant with propargylic acetates for the synthesis of terminal allenes is reported. Treatment of propargylic acetates with lithium butyl(phenylthio)cuprate in diethyl ether at -78°C yields the title compounds on workup with aqueous ammonium chloride.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 577-578 |
| Number of pages | 2 |
| Journal | Synthesis |
| Issue number | 6 |
| State | Published - 1993 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
A convenient terminal allene synthesis from propargylic acetates. / Nantz, M. H.; Bender, D. M.; Janaki, S.
In: Synthesis, No. 6, 1993, p. 577-578.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - A convenient terminal allene synthesis from propargylic acetates
AU - Nantz, M. H.
AU - Bender, D. M.
AU - Janaki, S.
PY - 1993
Y1 - 1993
N2 - The use of lithium butyl(phenylthio)cuprate as a reactant with propargylic acetates for the synthesis of terminal allenes is reported. Treatment of propargylic acetates with lithium butyl(phenylthio)cuprate in diethyl ether at -78°C yields the title compounds on workup with aqueous ammonium chloride.
AB - The use of lithium butyl(phenylthio)cuprate as a reactant with propargylic acetates for the synthesis of terminal allenes is reported. Treatment of propargylic acetates with lithium butyl(phenylthio)cuprate in diethyl ether at -78°C yields the title compounds on workup with aqueous ammonium chloride.
UR - http://www.scopus.com/inward/record.url?scp=0027241790&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027241790&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0027241790
SP - 577
EP - 578
JO - Synthesis (Germany)
JF - Synthesis (Germany)
SN - 0039-7881
IS - 6
ER -