Preparation of a psammaplysene-based library.
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Summary
A 28-member focused library, based on the pseudosymmetric template of the marine alkaloids psammaplysenes, was prepared from combinations of components that were, in turn, derived from 4-iodophenol.
- Type
- article
- Published
- 2006-09-14
- Cited by
- 15
- References
- 22
- Access
- Open access
- OpenAlex
- https://openalex.org/W2075147909
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:33924742
Keywords
Chemistry, Combinatorial chemistry, Stereochemistry, Nanotechnology, Computational biology
References
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- ON THE EFFICIENCY OF TETRAALKYLAMMONIUM SALTS IN HECK TYPE REACTIONS
- A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
- Fast, efficient and selective deprotection of the tert-butoxycarbonyl (Boc) group using HCl/dioxane (4 m).
- Synthesis of butadiyne-bridged [4n] metacyclophanes having exo-annular t-butyl groups
- Total synthesis of psammaplysenes A and B, naturally occurring inhibitors of FOXO1a nuclear export.
- A chemical genetic screen identifies inhibitors of regulated nuclear export of a Forkhead transcription factor in PTEN-deficient tumor cells.
- A convenient method for the selective reduction of amides to amines
- A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes
- The psammaplysenes, specific inhibitors of FOXO1a nuclear export.
- Highly regioselective ortho-chlorination of phenol with sulfuryl chloride in the presence of amines
- From protein domains to drug candidates-natural products as guiding principles in the design and synthesis of compound libraries.
- An efficient method for one-carbon elongation of aryl aldehydes via their dibromoalkene derivatives
- Allylic Bromination by N-Bromo-t-butylamine1
- Polyyne cyclization to form carbon cages: [16.16.16](1,3,5)cyclophanetetracosayne derivatives C60H6 and C60Cl6 as precursors to C60 fullerene
- Thermal- and microwave-assisted hydrogenation of electron-deficient alkenes using a polymer-supported hydrogen donor
- A Reiterative Approach to 2,3‐Disubstituted Naphthalenes and Anthracenes.
Cited by
- Genetic and pharmacological approaches to preventing neurodegeneration
- Regioselective iodination of phenol and analogues using N-iodosuccinimide and p-toluenesulfonic acid
- Recent Progress in the Use of N-Halo Compounds in Organic Synthesis
- FOXO3a is broadly neuroprotective in vitro and in vivo against insults implicated in motor neuron diseases
- Facile p-toluenesulfonic acid-promoted para-selective monobromination and chlorination of phenol and analogues
- Induction of apoptosis in endometrial cancer cells by psammaplysene A involves FOXO1
- Amphimedonoic acid and psammaplysene E, novel brominated alkaloids from Amphimedon sp.
- A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A
- Iodine(III)-Mediated, Controlled Di- or Monoiodination of Phenols.
- Base‐Promoted Double Amination of 1‐Haloalkynes: Direct Synthesis of Ene‐1,1‐diamines
- A novel H2S releasing-monastrol hybrid (MADTOH) inhibits L-type calcium channels
- Marine Brominated Tyrosine Alkaloids as Promising Inhibitors of SARS-CoV-2
- Water extract of pomegranate ash–I2 as sustainable system for external oxidant/metal/catalyst-free oxidative iodination of (hetero)arenes
- One-pot ipso-hydroxylation and ortho-/para-halogenation of (hetero)arylboronic acids under tungsten catalysis
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