BIOMAT Database Logo BIOMAT Database Logo

[Stereoselective synthesis of optically active vincamine]. 1975

P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth

UI MeSH Term Description Entries
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer
D014748 Vinca Alkaloids A group of indole-indoline dimers which are ALKALOIDS obtained from the VINCA genus of plants. They inhibit polymerization of TUBULIN into MICROTUBULES thus blocking spindle formation and arresting cells in METAPHASE. They are some of the most useful ANTINEOPLASTIC AGENTS. Alkaloids, Vinca

Related Publications

P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Synthesis of optically active trifluoromethylated indolizidine derivatives via stereoselective radical cyclization.
May 2002, Organic letters,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Asymmetric synthesis of deoxypolypropionate units via stereoselective hydrogenation of optically active cycloheptatriene.
November 2004, Organic letters,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Stereoselective synthesis of optically active 3-hydroxy-7,8-dihydro-beta-ionol-glucosides.
July 2003, Chemical & pharmaceutical bulletin,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Stereoselective and efficient total synthesis of optically active tetrodotoxin from D-glucose.
February 2008, The Journal of organic chemistry,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Lactones 42. Stereoselective enzymatic/microbial synthesis of optically active isomers of whisky lactone.
November 2013, Food chemistry,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Synthesis and stereoselective DNA binding abilities of new optically active open-chain polyamines.
March 2007, The Journal of organic chemistry,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Stereoselective synthesis of the optically active samin type of lignan from L-glutamic acid.
April 2000, Bioscience, biotechnology, and biochemistry,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Stereoselective model synthesis of the optically active olivil type of lignan from D-xylose.
August 2000, Bioscience, biotechnology, and biochemistry,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Stereoselective synthesis and thromboxane A2 (TXA2) receptor antagonistic activity of optically active phenol derivatives.
April 1996, Chemical & pharmaceutical bulletin,
P Pfäffli, and W Oppolzer, and R Wenger, and H Hauth
Synthesis and stereoselective halogenolysis of optically pure benzylstannanes.
March 2009, The Journal of organic chemistry,
Copied contents to your clipboard!