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Anticholinesterase Inhibitory Activity of Quaternary Alkaloids from Tinospora crispa
יצא לאור 2014"...Quaternary alkaloids are the major alkaloids isolated from Tinospora species. ..."
קבל טקסט מלא
קבל טקסט מלא
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102
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Silencing of tryptamine biosynthesis for production of nonnatural alkaloids in plant culture
יצא לאור 2010"...To exploit this chemically silent background, we introduced an unnatural tryptamine analog to the production media and demonstrated that the silenced plant culture could produce a variety of novel products derived from this unnatural starting substrate. The novel alkaloids were not contaminated by the presence of the natural alkaloids normally present in C. roseus. ..."
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104
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Isolation of the pyrrolizidine alkaloid 1-epialexine from Castanospermum australe
יצא לאור 2010"...The Australian leguminous tree Castanospermum australe contains the anti-viral glucose analogue indolizidine alkaloid castanospermine. As the result of a search for new bioactive carbohydrate-like compounds we now report the isolation of the novel polyhydroxylated pyrrolizidine alkaloid, 1-epialexine, from the leaves and stems of C. australe. 1-Epialexine is a weak inhibitor of β-mannosidase from Cellullomonas fimi. © 2010 Phytochemical Society of Europe...."
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A practical and scaleable total synthesis of the jaborandi alkaloid (+)-pilocarpine
יצא לאור 2009Journal article -
110
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Investigation into the absolute stereochemistry of the marine sponge alkaloid pyrinodemin A
יצא לאור 2003"...The absolute configuration of the marine sponge alkaloid pyrinodemin A is established by organic synthesis. © 2003 Elsevier Ltd. ..."
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112
ORGN 549-Cascade approaches to the total synthesis of the lepadin alkaloids
יצא לאור 2008Conference item -
113
Bifunctional organo/metal cooperative catalysis with cinchona alkaloid scaffolds
יצא לאור 2012"...This review discusses recent developments (the last 10 years) in the field of cooperative catalysis using cinchona alkaloid derivatives in combination with metal ions, highlighting the potential of this new research area and the many challenges that still remain for the future. ..."
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114
Steviamine, a new indolizidine alkaloid from Stevia rebaudiana
יצא לאור 2010"...This is the first report of an indolizidine iminosugar alkaloid from the Asteraceae and Hyacinthaceae. Steviamine may occur in some Stevia products and influence taste. © 2010 Phytochemical Society of Europe...."
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115
Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
יצא לאור 2002"...The total synthesis of two cytotoxic sponge alkaloids hachijodines F (1) and G (2) via a common intermediate 3 is described. © 2002 Elsevier Science Ltd. ..."
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116
Asymmetric syntheses of the homalium alkaloids (-)-(S,S)-homaline and (-)-(R,R)-hopromine.
יצא לאור 2012"...The highly diastereoselective conjugate additions of the novel lithium amide reagents lithium (R)-N-(3-chloropropyl)-N-(α-methylbenzyl)amide and lithium (R)-N-(3-chloropropyl)-N-(α-methyl-p-methoxybenzyl)amide to α,β-unsaturated esters were used as the key steps in syntheses of the homalium alkaloids (-)-(S,S)-homaline and (-)-(R,R)-hopromine. ..."
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117
Strategies towards the synthesis of calyciphylline A-type Daphniphyllum alkaloids.
יצא לאור 2014"...The Daphniphyllum alkaloids are a diverse family of natural products rich in number and structural diversity that have been known for many decades. ..."
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118
GLYCOSIDASE INHIBITION BY PLANT ALKALOIDS WHICH ARE STRUCTURAL ANALOGS OF MONOSACCHARIDES
יצא לאור 1985"...]The inhibitory activities of three plant alkaloids, deoxynojirimycin, 2,5-dihydroxymethyl-3,4-dihydroxypyrrolidine and 1,5 dideoxy-1,5-imino-D-mannitol towards glycosidases from several sources have been compared. ..."
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Total synthesis of cytotoxic sponge alkaloids Motuporamines A and B
יצא לאור 1999"...The synthesis of two sponge alkaloids, Motuporamines A and B is reported. The key step involved a reductive amination using sodium triacetoxyborohydride...."
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Total synthesis of cytotoxic sponge alkaloids hachijodines F and G
יצא לאור 2003"...The total synthesis of two cytotoxic sponge alkaloids hachijodines F and G has been achieved. The synthesis of both compounds utilises a common intermediate alkyne. ..."
Journal article