Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jochen Weckesser"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 28 (2010)
Norborn-5-ene-(N,N-dipyrid-2-yl)carbamide (M1) was copolymerized with exo,exo-[2-(3-ethoxycarbonyl-7-oxabicyclo[2.2.1]hept-5-en-2-carbonyloxy)ethyl]trimethylammonium iodide (M2) using the Schrock catalyst Mo(N-2,6-Me2-C6H3)(CHCMe2Ph)(OCMe(CF3)2)2 [Mo
Externí odkaz:
https://doaj.org/article/da8c4fc1a8eb4de0924c4b2778b3522d
Publikováno v:
European Journal of Organic Chemistry. 2013:1346-1355
Herein, we report on the first enantioselective synthesis of the sparteine-type alkaloids virgidivarine (1) and virgiboidine (2). The stereoselective construction of the challenging dipiperidine core within 1 and 2 was realized by applying an intramo
Publikováno v:
Applied Organometallic Chemistry. 22:211-214
The Rh-catalyzed cycloisomerization of new terpenoid derivatives featuring an O-tethered enyne unexpectedly leads to polycyclic derivatives containing an inner cyclopropane ring or a diene moiety, depending on the structure of the enyne, as observed
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 28 (2010)
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 28 (2010)
Norborn-5-ene-(N,N-dipyrid-2-yl)carbamide (M1) was copolymerized with exo,exo-[2-(3-ethoxycarbonyl-7-oxabicyclo[2.2.1]hept-5-en-2-carbonyloxy)ethyl]trimethylammonium iodide (M2) using the Schrock catalyst Mo(N-2,6-Me2-C6H3)(CHCMe2Ph)(OCMe(CF3)2)2 [Mo
Autor:
Michael R. Buchmeiser, Siegfried Blechert, Bhasker Bantu, Gajanan M. Pawar, Klaus Wurst, Jochen Weckesser
Publikováno v:
Dalton Transactions. :9043
Ring-opening metathesis polymerization has been used for the synthesis of the amphiphilic block-copolymer poly(M1-co-M3)-b-poly(M2) from the hydrophilic monomer 5-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxymethyl}-7-oxabicyclo[2.2.1]hept-2-ene (M2), and
Autor:
Gajanan M. Pawar, Bhasker Bantu, Jochen Weckesser, Siegfried Blechert, Klaus Wurst, Michael R. Buchmeiser
Publikováno v:
Dalton Transactions: An International Journal of Inorganic Chemistry; Oct2009, Vol. 2009 Issue 41, p9043-9051, 9p
Autor:
Kress, Steffen1, Weckesser, Jochen1, Schulz, Sabrina Renate1, Blechert, Siegfried1 blechert@chem.tu‐berlin.de
Publikováno v:
European Journal of Organic Chemistry. Mar2013, Vol. 2013 Issue 7, p1346-1355. 10p.
Autor:
Kreß, Steffen
In der vorliegenden Arbeit wird die enantioselektive Totalsynthese des Dipiperidin-Alkaloids Virgidivarin (1) und die des Piperidino-Chinolizidins Virgiboidin (2) beschrieben. 2 geht aus der freien Aminosäure 1 durch Zyklisierung unter Amidbildung h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5250c295ceba23d0447041fe5ae11786
http://depositonce.tu-berlin.de/handle/11303/3864
http://depositonce.tu-berlin.de/handle/11303/3864
Autor:
Costes, Philippe, Weckesser, Jochen, Dechy-Cabaret, Odile, Urrutigoïty, Martine, Kalck, Philippe
Publikováno v:
Applied Organometallic Chemistry; Apr2008, Vol. 22 Issue 4, p211-214, 4p