Uncatalysed diaryldiazo cyclopropanations on bicyclic lactams: access to annulated prolines.

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Uncatalysed diaryldiazo cyclopropanations on bicyclic lactams: access to annulated prolines.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

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Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

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Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

@en

Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

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Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

@en

Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

@nl

P1476

Uncatalysed diaryldiazo cyclop ...... access to annulated prolines.

@en

P2093

Amber L Thompson

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Andrew R Cowley

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Martin Gilpin

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P2860

Amino acidic scaffolds bearing unnatural side chains: an old idea generates new and versatile tools for the life sciences

Total Syntheses of Epothilones A and B via a Macrolactonization-Based Strategy

Photolysis of chiral 1-pyrazolines to cyclopropanes: mechanism and stereospecificity.

Ligands for glutamate receptors: design and therapeutic prospects.

Design, synthesis, and pharmacological characterization of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740): a potent, selective, and orally active group 2 metabotropic glutamate receptor agonist possessing anticonvulsant and anxioly

Synthesis and metabotropic glutamate receptor activity of S-oxidized variants of (-)-4-amino-2-thiabicyclo-[3.1.0]hexane-4,6-dicarboxylate: identification of potent, selective, and orally bioavailable agonists for mGlu2/3 receptors.

Rhodium-catalyzed enantioselective cyclopropanation of electron deficient alkenes.

The use of spirocyclic scaffolds in drug discovery.

Biosynthesis of penicillin N and cephalosporin C. Antibiotic production and other features of the metabolism of Cephalosporium sp.

Discovery of (1R,5S)-N-[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]- 3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]- 6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (SCH 503034), a selective, potent, orally bio

P304

6522-6550

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scholarly article

P356

10.1039/C5OB00648A

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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Mark G. Moloney

Lawrence D Harris

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2015-05-15T00:00:00Z

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25975925

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