Details
| Original language | English |
|---|---|
| Pages (from-to) | 1104-1106 |
| Number of pages | 3 |
| Journal | SYNLETT |
| Issue number | 7 |
| Publication status | Published - 2010 |
Abstract
Amides undergo Hofmann rearrangement by treatment with (diacetoxyiodo) benzene (DAIB) to provide symmetrical ureas in a simple and robust transformation.
Keywords
- Carbamates, Diacetoxyiodobenzene, Hofmann rearrangement, Ureas
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: SYNLETT, No. 7, 2010, p. 1104-1106.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Synthesis of symmetrical ureas by (Diacetoxyiodo)benzene-induced hofmann rearrangement
AU - Landsberg, Dirk
AU - Kalesse, Markus
PY - 2010
Y1 - 2010
N2 - Amides undergo Hofmann rearrangement by treatment with (diacetoxyiodo) benzene (DAIB) to provide symmetrical ureas in a simple and robust transformation.
AB - Amides undergo Hofmann rearrangement by treatment with (diacetoxyiodo) benzene (DAIB) to provide symmetrical ureas in a simple and robust transformation.
KW - Carbamates
KW - Diacetoxyiodobenzene
KW - Hofmann rearrangement
KW - Ureas
UR - http://www.scopus.com/inward/record.url?scp=77951095107&partnerID=8YFLogxK
U2 - 10.1055/s-0029-1219566
DO - 10.1055/s-0029-1219566
M3 - Article
AN - SCOPUS:77951095107
SP - 1104
EP - 1106
JO - SYNLETT
JF - SYNLETT
SN - 0936-5214
IS - 7
ER -