Abstract
A convenient preparation of the aromatic segment 3 starting from 3,5-dibromo-2,6-dimethoxytoluene 5 and furan was described along with the elaboration of 3 by the aldol coupling with the aliphatic segment 2 to the synthetic precursor 4 of rifamycin W.
| Original language | English |
|---|---|
| Pages (from-to) | 1373-1376 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 25 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - 1984 |
Fingerprint
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
Synthetic studies of rifamycins. VI. Preparation and elaboration of the aromatic segment for the synthesis of rifamycin W. / Nakata, Masaya; Kinoshita, Mitsuhiro; Ohba, Shigeru; Saito, Yoshihiko.
In: Tetrahedron Letters, Vol. 25, No. 13, 1984, p. 1373-1376.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Synthetic studies of rifamycins. VI. Preparation and elaboration of the aromatic segment for the synthesis of rifamycin W
AU - Nakata, Masaya
AU - Kinoshita, Mitsuhiro
AU - Ohba, Shigeru
AU - Saito, Yoshihiko
PY - 1984
Y1 - 1984
N2 - A convenient preparation of the aromatic segment 3 starting from 3,5-dibromo-2,6-dimethoxytoluene 5 and furan was described along with the elaboration of 3 by the aldol coupling with the aliphatic segment 2 to the synthetic precursor 4 of rifamycin W.
AB - A convenient preparation of the aromatic segment 3 starting from 3,5-dibromo-2,6-dimethoxytoluene 5 and furan was described along with the elaboration of 3 by the aldol coupling with the aliphatic segment 2 to the synthetic precursor 4 of rifamycin W.
UR - http://www.scopus.com/inward/record.url?scp=0021351127&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0021351127&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(01)80161-1
DO - 10.1016/S0040-4039(01)80161-1
M3 - Article
AN - SCOPUS:0021351127
VL - 25
SP - 1373
EP - 1376
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 13
ER -