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「Org Biomol Chem[Journal]」の検索結果

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Synthesis of 1,4-diazepinone derivatives via a domino aza-Michael/S2 cyclization of 1-azadienes with α-halogenoacetamides.

Site-selective protein modification via disulfide rebridging for fast tetrazine/trans-cyclooctene bioconjugation.

Recent advances in the direct β-C(sp)-H functionalization of enamides.

Recent progress in the total synthesis of Strychnos alkaloids.

A lysosome-targeted near-infrared fluorescent probe for imaging of acid phosphatase in living cells.

Biomimetic total syntheses of baefrutones A-D, baeckenon B, and frutescones A, D-F.

Self-assembling purine and pteridine quartets: how do π-conjugation patterns affect resonance-assisted hydrogen bonding?

Recent progress in the total synthesis of marine brominated sesquiterpene aplydactone.

Visible-light-mediated photocatalytic cross-coupling of acetenyl ketones with benzyl trifluoroborate.

Solid-phase synthesis of branched oligonucleotides containing a biologically relevant dCyd341 interstrand crosslink DNA lesion.

Substituent-controlled chemoselective synthesis of multi-substituted pyridones via a one-pot three-component cascade reaction.

Synthetic approaches towards avibactam and other diazabicyclooctane β-lactamase inhibitors.

Visible-light-promoted radical cross-coupling of para-quinone methides with N-substituted anilines: an efficient approach to 2,2-diarylethylamines.

Looking at the big picture in activation strain model/energy decomposition analysis: the case of the ortho-para regioselectivity rule in Diels-Alder reactions.

Synthesis and glycosidase inhibition of N-substituted derivatives of 1,4-dideoxy-1,4-imino-d-mannitol (DIM).

Probing the helical integrity of multivicinal all-syn-fluoro alkanes.

The endo-aza-Michael addition in the synthesis of piperidines and pyrrolidines.

Copper-catalysed synthesis of 3-hydroxyisoindolin-1-ones from benzylcyanide 2-iodobenzamides.

Rhodium-catalyzed asymmetric hydrogenation of exocyclic α,β-unsaturated carbonyl compounds.

Photo-induced glycosylation using a diaryldisulfide as an organo-Lewis photoacid catalyst.

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