Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Andreas Lanver"'
Autor:
Hans-Günther Schmalz, Andreas Lanver
Publikováno v:
European Journal of Organic Chemistry. 2005:1444-1458
The synthesis of three new carbocyclic nucleoside analogs (CNAs) with the nucleobase attached to a 3′-hydroxymethylcyclopent-2′-en-1′-yl scaffold is reported. A variety of symmetric dienynes (propargylic acetals of type 11) were used as substra
Autor:
Andreas Lanver, Hans-Günther Schmalz
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules; Volume 10; Issue 2; Pages: 508-515
Molecules, Vol 10, Iss 2, Pp 508-515 (2005)
Molecules; Volume 10; Issue 2; Pages: 508-515
Molecules, Vol 10, Iss 2, Pp 508-515 (2005)
An efficient protocol for the amination of 6-chloropurine derivatives through nucleophilic aromatic substitution under microwave irradiation was developed and applied to the synthesis in two steps of a series of new acyclic nucleosides (acyclovir ana
Autor:
Siguo Yuan, Andreas Lanver, David C. Sherrington, Hans-Günther Schmalz, B. Wilson, Xiongwei Ni
Publikováno v:
Angewandte Chemie International Edition. 41:3656-3659
Both macroporous and gel-type high-quality spherical particulate styrene-divinylbenzene resins (see representative optical micrograph) can be synthesized in good yield on a small scale by using an oscillatory baffled reactor. The methodology is toler
Autor:
Philippe Dagneau, Dimitrios E. Lizos, Stellios Arseniyadis, Kyriacos C. Nicolaou, Raffaella Faraoni, Andreas Lanver, Adrian Ortiz, Hongjun Zhang, Michael P. Jennings
Publikováno v:
ChemInform. 41
The total synthesis of the originally assigned structure of vannusal B (2) and its diastereomer (d-2) are described. Initial forays into these structures with model systems revealed the viability of a metathesis-based approach and a SmI2-mediated str
Autor:
Raffaella Faraoni, Stellios Arseniyadis, Philippe Dagneau, Kyriacos C. Nicolaou, Dimitrios E. Lizos, Andreas Lanver, Michael P. Jennings, Hongjun Zhang, Adrian Ortiz
Publikováno v:
Journal of the American Chemical Society. 132(20)
The total synthesis of the originally assigned structure of vannusal B (2) and its diastereomer (d-2) are described. Initial forays into these structures with model systems revealed the viability of a metathesis-based approach and a SmI(2)-mediated s
Autor:
Andreas Lanver, Hans‐Guenther Schmalz
Publikováno v:
ChemInform. 36
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 10(20)
A diversity-oriented, enantioselective synthesis of new (monoprotected) carbocyclic nucleoside analogues (CNAs) with the nucleobase attached to a 3-hydroxymethyl-4-trialkylsilyloxymethylcyclopent-2-en-1-yl scaffold was developed. As a key intermediat
Autor:
David C, Sherrington, Andreas, Lanver, Hans-Günther, Schmalz, Bruce, Wilson, Xiong-Wei, Ni, Siguo, Yuan
Publikováno v:
Angewandte Chemie (International ed. in English). 41(19)
Autor:
Andreas Lanver, Hans-Gnther Schmalz
Publikováno v:
European Journal of Organic Chemistry; Apr2005, Vol. 2005 Issue 7, p1444-1458, 15p
Publikováno v:
Chemistry - A European Journal; Oct2004, Vol. 10 Issue 20, p5087-5110, 24p