Abstract
A total synthesis of aplysiatoxin was achieved formally by construction of Kishi's intermediate 13 which carried all the stereochemistry required for the synthesis of aplysiatoxin, from four fragments described in the preceding communication.
| Original language | English |
|---|---|
| Pages (from-to) | 5141-5142 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 32 |
| Issue number | 38 |
| DOIs | |
| Publication status | Published - Sep 16 1991 |
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All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry
Cite this
A formal total synthesis of aplysiatoxin. / Okamura, Hiroaki; Kuroda, Satoru; Ikegami, Satoru; Ito, Yoshio; Katsuki, Tsutomu; Yamaguchi, Masaru.
In: Tetrahedron Letters, Vol. 32, No. 38, 16.09.1991, p. 5141-5142.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - A formal total synthesis of aplysiatoxin
AU - Okamura, Hiroaki
AU - Kuroda, Satoru
AU - Ikegami, Satoru
AU - Ito, Yoshio
AU - Katsuki, Tsutomu
AU - Yamaguchi, Masaru
PY - 1991/9/16
Y1 - 1991/9/16
N2 - A total synthesis of aplysiatoxin was achieved formally by construction of Kishi's intermediate 13 which carried all the stereochemistry required for the synthesis of aplysiatoxin, from four fragments described in the preceding communication.
AB - A total synthesis of aplysiatoxin was achieved formally by construction of Kishi's intermediate 13 which carried all the stereochemistry required for the synthesis of aplysiatoxin, from four fragments described in the preceding communication.
UR - http://www.scopus.com/inward/record.url?scp=0025767868&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025767868&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(00)93449-X
DO - 10.1016/S0040-4039(00)93449-X
M3 - Article
AN - SCOPUS:0025767868
VL - 32
SP - 5141
EP - 5142
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 38
ER -