Abstract
Structural, kinetic, and spectroscopic studies show that the mechanism for the thiation of organic carbonyls by Lawesson's reagent involves momomeric RPS2 intermediates.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3445-3448 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 27 |
| Issue number | 30 |
| DOIs | |
| State | Published - 1986 |
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ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Cite this
Mechanistic studies on the thiation of carbonyls by Lawesson's reagent : The role of a 3-coordinate phosphorus(V) species. / Rauchfuss, Thomas; Zank, Gregg A.
In: Tetrahedron Letters, Vol. 27, No. 30, 1986, p. 3445-3448.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Mechanistic studies on the thiation of carbonyls by Lawesson's reagent
T2 - The role of a 3-coordinate phosphorus(V) species.
AU - Rauchfuss, Thomas
AU - Zank, Gregg A.
PY - 1986
Y1 - 1986
N2 - Structural, kinetic, and spectroscopic studies show that the mechanism for the thiation of organic carbonyls by Lawesson's reagent involves momomeric RPS2 intermediates.
AB - Structural, kinetic, and spectroscopic studies show that the mechanism for the thiation of organic carbonyls by Lawesson's reagent involves momomeric RPS2 intermediates.
UR - http://www.scopus.com/inward/record.url?scp=0000442629&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0000442629&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)84818-2
DO - 10.1016/S0040-4039(00)84818-2
M3 - Article
AN - SCOPUS:0000442629
VL - 27
SP - 3445
EP - 3448
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 30
ER -