Progress in fumagillin synthesis
Gespeichert in:
Verfasser / Beitragende:
[W. Picoul, O. Bedel, A. Haudrechy, Y. Langlois]
Ort, Verlag, Jahr:
2003
Enthalten in:
Pure and Applied Chemistry, 75/2-3(2003-01-01), 235-249
Format:
Artikel (online)
Online Zugang:
| LEADER | caa a22 4500 | ||
|---|---|---|---|
| 001 | 378866362 | ||
| 003 | CHVBK | ||
| 005 | 20180305123358.0 | ||
| 007 | cr unu---uuuuu | ||
| 008 | 161128e20030101xx s 000 0 eng | ||
| 024 | 7 | 0 | |a 10.1351/pac200375020235 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1351/pac200375020235 | ||
| 245 | 0 | 0 | |a Progress in fumagillin synthesis |h [Elektronische Daten] |c [W. Picoul, O. Bedel, A. Haudrechy, Y. Langlois] |
| 520 | 3 | |a After a brief account of the syntheses previously described in literature, several approaches of the antiangiogenic sesquiterpene fumagillin are described. Particularly, a Claisen-Ireland ring-closing metathesis strategy allowed the stereoselective preparation of several advanced intermediates in the fumagillin synthesis. | |
| 540 | |a © 2013 Walter de Gruyter GmbH, Berlin/Boston | ||
| 700 | 1 | |a Picoul |D W. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | |
| 700 | 1 | |a Bedel |D O. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | |
| 700 | 1 | |a Haudrechy |D A. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | |
| 700 | 1 | |a Langlois |D Y. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | |
| 773 | 0 | |t Pure and Applied Chemistry |d De Gruyter |g 75/2-3(2003-01-01), 235-249 |x 0033-4545 |q 75:2-3<235 |1 2003 |2 75 |o pac | |
| 856 | 4 | 0 | |u https://doi.org/10.1351/pac200375020235 |q text/html |z Onlinezugriff via DOI |
| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1351/pac200375020235 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Picoul |D W. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Bedel |D O. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Haudrechy |D A. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Langlois |D Y. |u Laboratoire de Synthèse des Substances Naturelles,Associé au CNRS, Université de Paris-Sud, F-91405 Orsay, France |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Pure and Applied Chemistry |d De Gruyter |g 75/2-3(2003-01-01), 235-249 |x 0033-4545 |q 75:2-3<235 |1 2003 |2 75 |o pac | ||
| 900 | 7 | |b CC0 |u http://creativecommons.org/publicdomain/zero/1.0 |2 nationallicence | |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||