Abstract
CC bond formation through reactions of iododifluoroacetate-copper with various organic halides in aprotic solvent proceeds effectively to give 2,2-difluoroesters in good yield. With alkenyl iodides, these reactions are stereospecific.
| Original language | English |
|---|---|
| Pages (from-to) | 6103-6106 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 27 |
| Issue number | 50 |
| DOIs | |
| Publication status | Published - 1986 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Synthesis of 2,2-difluoroesters by iododifluoroacetate-copper with organic halides. / Taguchi, Takeo; Kitagawa, Osamu; Morikawa, Tsutomu; Nishiwaki, Tohru; Uehara, Hideya; Endo, Hatsumi; Kobayashi, Yoshiro.
In: Tetrahedron Letters, Vol. 27, No. 50, 1986, p. 6103-6106.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthesis of 2,2-difluoroesters by iododifluoroacetate-copper with organic halides
AU - Taguchi, Takeo
AU - Kitagawa, Osamu
AU - Morikawa, Tsutomu
AU - Nishiwaki, Tohru
AU - Uehara, Hideya
AU - Endo, Hatsumi
AU - Kobayashi, Yoshiro
PY - 1986
Y1 - 1986
N2 - CC bond formation through reactions of iododifluoroacetate-copper with various organic halides in aprotic solvent proceeds effectively to give 2,2-difluoroesters in good yield. With alkenyl iodides, these reactions are stereospecific.
AB - CC bond formation through reactions of iododifluoroacetate-copper with various organic halides in aprotic solvent proceeds effectively to give 2,2-difluoroesters in good yield. With alkenyl iodides, these reactions are stereospecific.
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UR - http://www.scopus.com/inward/citedby.url?scp=0001186360&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)85409-X
DO - 10.1016/S0040-4039(00)85409-X
M3 - Article
AN - SCOPUS:0001186360
VL - 27
SP - 6103
EP - 6106
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 50
ER -