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The Castle Synthesis of (-)-Acutumine

Chemexpress May 22, 2024 0 Comments

The complex tetracyclic alkaloid (-)-acutumine 3, isolated from the Asian vine Menispermum dauricum, shows selective T-cell toxicity. The two adjacent cyclic all-carbon quaternary centers of 3 offered a particular challenge.…

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The Carter Synthesis of (-)-Lycopodine

Chemexpress May 22, 2024 0 Comments

Rich G. PMID:23381626 Carter of Oregon State University described (J. Am. Chem. Soc. 2008, 130, 9238 DOI: 10.1021/ja803613w) the first enantioselective synthesis of the Lycopodium alkaloid (-)-lyopodine (3). A key…

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The Overman Syntheses of Nankakurines A and B

Chemexpress May 22, 2024 0 Comments

The tetracyclic alkaloids Nankakurine A and Nankakurine B were isolated from the club moss Lycopodium hamiltonii. A preliminary study of the biological activity of Nankakurine A suggested that it could…

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The Kobayashi Synthesis of (-)-Norzoanthamine

Chemexpress May 22, 2024 0 Comments

The Zoanthus alkaloids, exemplified by (-)-norzoanthamine (3a) and zoanthamine (3b), show promising activity against osteoporosis. PMID:24189672 Susumu Kobayashi of the Tokyo University of Science assembled (Angew. Chem. Int. Ed. 2009,…

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The Zakarian Synthesis of (+)-Pinnatoxin A

Chemexpress May 22, 2024 0 Comments

(+)-Pinnatoxin A (3), isolated from the shellfish Pinna muricata, is thought to be a calcium channel activator. A key transformation in the synthesis of 3 reported (J. Am. Chem. Soc.…

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N and theCharacterization in the mAbThe cross reactivity on the mAb

Chemexpress May 21, 2024 0 Comments

N and theCharacterization of your mAbThe cross reactivity in the mAb 2G12E1 was tested using artesunate, dihydroartemisinin, artemisinin along with other important antimalarial drugs in icELISA (Table 1). The cross…

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Ug/ml. Following choice, steady clones were isolated by limiting dilution.

Chemexpress May 21, 2024 0 Comments

Ug/ml. Following selection, steady clones have been isolated by limiting dilution. Knockdown was monitored by operating complete cell lysates and/or spent media on gels and probing with versican antibodies as…

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The Johnson Synthesis of Zaragozic Acid C

Chemexpress May 21, 2024 0 Comments

The zaragozic acids, exemplified by Zaragozic Acid C (3), are picomolar inhibitors of cholesterol biosynthesis. Jeffrey S. PMID:26446225 2126818-91-3 custom synthesis Johnson of the University of North Carolina developed (J.…

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The Paquette Synthesis of Fomannosin

Chemexpress May 21, 2024 0 Comments

The compact sesquiterpene (+)-fomannosin (3), isolated from the pathogenic fungus Fomes annonsus, presents an interesting set of challenges for the organic synthesis chemist, ranging from the strained cyclobutene to the…

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Oxidative Heck Arylations

Chemexpress May 21, 2024 0 Comments

A recent publication by Mats Larhed and co-workers from Uppsala University (J. Org. 5-Chloro-4-methylpyridin-3-amine Purity Chem. 2004, 69, 5212.DOI: 10.1021/jo049434t)describes dioxygen-promoted regioselective oxidativeHeck arylations of electron-rich olefins with arylboronic acids.…

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2-amino-N-cyclopentylpropanamide hydrochloride (CAS 1214638-91-1)

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