Search Results - "Aceña, J L"
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FM19G11 reverses endothelial dysfunction in rat and human arteries through stimulation of the PI3K/Akt/eNOS pathway, independently of mTOR/HIF‐1α activation
Published in British journal of pharmacology (01-03-2015)“…Background and Purpose FM19G11 up‐regulates mammalian target of rapamycin (mTOR)/hypoxia inducible factor‐1α (HIF‐1α) and PI3K/Akt pathways, which are involved…”
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Quantitative analysis of ES-285, an investigational marine anticancer drug, in human, mouse, rat, and dog plasma using coupled liquid chromatography and tandem mass spectrometry
Published in Journal of mass spectrometry. (01-05-2003)“…A method was developed for the quantitative analysis of the novel anticancer agent ES‐285 (spisulosine; free base) in human, mouse, rat, and dog plasma using…”
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Total Synthesis of (+)-7-Deoxypancratistatin from Furan
Published in Organic letters (16-11-2000)“…A new total synthesis of (+)-7-deoxypancratistatin 1 has been accomplished in 19 steps (8% overall yield) from two readly available compounds, furan and…”
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Total Syntheses of (±)-Cyclophellitol and (1R,6S)-Cyclophellitol
Published in Journal of organic chemistry (16-05-1997)“…A stereodivergent synthesis of (±)-cyclophellitol (1) and its unnatural diastereoisomer (1R*,6S*)-cyclophellitol (2), starting from the Diels−Alder adduct of…”
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Studies in Marine Polypropionate Synthesis: Total Synthesis of (−)-Baconipyrone C
Published in Organic letters (01-06-2000)“…An asymmetric total synthesis of the unusual siphonariid metabolite, (−)-baconipyrone C (3), is described. Key steps included a tin(II)-mediated aldol coupling…”
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FM19G11 reverses endothelial dysfunction in rat and human arteries through stimulation of the PI3K/Akt/eNOS pathway, independently of mTOR/HIF-1[alpha] activation
Published in British journal of pharmacology (01-03-2015)“…Background and Purpose FM19G11 up-regulates mammalian target of rapamycin (mTOR)/hypoxia inducible factor-1[alpha] (HIF-1[alpha]) and PI3K/Akt pathways, which…”
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Role of the gem-Difluoro Moiety in the Tandem Ring-Closing Metathesis−Olefin Isomerization: Regioselective Preparation of Unsaturated Lactams
Published in Journal of organic chemistry (31-03-2006)“…Careful selection of the metathesis catalyst, solvent, and reaction conditions allows for the efficient and regioselective synthesis of isomeric fluorinated…”
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Fluorous (Trimethylsilyl)ethanol: A New Reagent for Carboxylic Acid Tagging and Protection in Peptide Synthesis
Published in Journal of organic chemistry (14-04-2006)“…Starting with a fluorous analogue of 2-(trimethylsilyl)ethanol, we have designed an easy method for preparing a new fluorous tag (FTMSE) for the protection of…”
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Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1
Published in Angewandte Chemie International Edition (05-11-2001)“…As an exceptionally potent antimitotic macrolide, altohyrtin A/spongistatin 1 shows great promise in cancer chemotherapy but its extreme scarcity in the…”
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The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation
Published in Organic & biomolecular chemistry (07-07-2005)“…The antimitotic marine macrolide altohyrtin A/spongistatin 1 has been synthesised in a highly convergent and stereocontrolled manner, thus contributing to the…”
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Synthesis and Biological Evaluation of New Bicyclic Fluorinated Uracils through Ring-Closing Metathesis
Published in Journal of organic chemistry (12-05-2006)“…Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis…”
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The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment
Published in Organic & biomolecular chemistry (07-07-2005)“…The fully functionalised C29-C51 southern hemisphere of altohyrtin A/spongistatin 1 , incorporating the E- and F-ring tetrahydropyran rings and the unsaturated…”
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Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncation
Published in Chemical communications (Cambridge, England) (21-02-2003)“…Simplified analogues of the potent antimitotic marine macrolide spongistatin 1/altohyrtin A were synthesised and evaluated as growth inhibitory agents against…”
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Unexpected One-Pot Epoxy Sulfone−Enaminone Transformation. Synthesis of 5a-Carba-β-mannopyranosylamine
Published in Journal of organic chemistry (21-04-2000)Get full text
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New fluorinated 1,3-vinylogous amidines as versatile intermediates: synthesis of fluorinated pyrimidin-2(1 H)-ones
Published in Tetrahedron (13-02-2006)“…The condensation of the azaenolates derived from readily available ketimines with fluorinated nitriles offers an efficient and straightforward entry to new…”
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Polypropionates from 7-oxanorbornene derivatives. A stereoselective and divergent synthesis of fragments with four contiguous chiral centers
Published in Tetrahedron letters (02-12-1996)“…The epimeric stereotetrads 12 and 14 have been prepared starting from the Diels-Alder endo adduct of furan and acrylic acid. The key steps of the route were…”
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A convenient approach to the aminocyclitol fragment of pancratistatin from 7-oxanorbornenes
Published in Tetrahedron letters (1996)“…A totally stereoselective route to an analogue aminocyclitol fragment of the alkaloid pancratistatin has been achieved starting from a 7-oxanorbornenic…”
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Total synthesis of (+)-pinitol
Published in Tetrahedron: asymmetry (01-12-1996)“…A new synthesis of (+)-pinitol 9 has been developed starting from the 7-oxanorbornenic sulfone (+)- 5, prepared in enantiomerically pure form by resolution of…”
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