Results 41 to 50 of about 14,944,148 (406)
Phyllostictine A : total synthesis, structural verification and determination of substructure responsible for plant growth inhibition [PDF]
The first total synthesis of phyllostictine A (PA) is reported, which confirms the structure of this fungal metabolite and its (6S,7R,8S)-stereochemistry.
Clarkson, Guy J. +6 more
core +1 more source
Enantioselective Synthesis of 5-epi-Citreoviral Using Ruthenium-Catalyzed Asymmetric Ring-Closing Metathesis [PDF]
Chiral ruthenium olefin metathesis catalysts can perform asymmetric ring-closing reactions in ≥90% ee with low catalyst loadings. To illustrate the practicality of these reactions and the products they form, an enantioselective total synthesis of 5-epi ...
Funk, Timothy W.
core +2 more sources
A chemoselective and continuous synthesis of m-sulfamoylbenzamide analogues [PDF]
For the synthesis of m-sulfamoylbenzamide analogues, small molecules which are known for their bioactivity, a chemoselective procedure has been developed starting from m-(chlorosulfonyl) benzoyl chloride.
Heugebaert, Thomas +5 more
core +3 more sources
Total Synthesis of (−)-Reveromycin A [PDF]
The asymmetric total synthesis of (-)-reveromycin A is described. The key steps involved a Lewis acid catalyzed inverse electron demand hetero-Diels-Alder reaction followed by hydroboration/oxidation to afford the spiroketal core 4 in a highly stereoselective manner and introduction of the C18 hemisuccinate by high-pressure acylation.
El Sous, Mariana +3 more
openaire +3 more sources
Recent advances in the total synthesis of agelastatins [PDF]
Agelastatins represent an important family of marine alkaloids in terms of both exceptional biological activity and intriguing chemical structure.
Dong, Guangbin
core +1 more source
Xylochemical Synthesis and Biological Evaluation of Shancigusin C and Bletistrin G
The biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses.
Leander Geske +6 more
doaj +1 more source
Total synthesis of rhizopodin. [PDF]
This is the peer reviewed version of the following article: Dalby, S.M, Goodwin-Tindall, J., Paterson, I. (2013), Total Synthesis of (−)-Rhizopodin. Angew. Chem. Int.
Dieckmann, Michael +5 more
core +1 more source
Synthesis of the Sex Pheromone of the Tea Tussock Moth Based on a Resource Chemistry Strategy
Synthesis of the sex pheromone of the tea tussock moth in 33% overall yield over 10 steps was achieved. Moreover, the chiral pool concept was applied in the asymmetric synthesis.
Hong-Li Zhang +5 more
doaj +1 more source
Total synthesis of (±)-paroxetine by diastereoconvergent cobalt-catalysed arylation
A total synthesis of paroxetine is reported, with a diastereoselective and diastereoconvergent cobalt-catalysed sp3–sp2 coupling reaction involving a 3-substituted 4-bromo-N-Boc-piperidine (Boc = tert-butoxycarbonyl) substrate as a key step.
Despiau, Carole F. +3 more
core +2 more sources

