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Microbial cyclosophoraose as a catalyst for the synthesis of diversified...

Green Chemistry International Green Chem., 2016, 18,3620-3627DOI: 10.1039/C6GC00137H, Paper Someshwar D. Dindulkar, Daham Jeong, Eunae Cho, Dongjin Kim, Seunho Jung A novel biosourced saccharide...

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Visible-light-activated copper(I) catalyzed oxidative Csp–Csp cross-coupling...

Green Chemistry International A novel visible-light-promoted copper-catalysed process for the Csp–Csp cross-coupling reaction of terminal alkynes at room temperature is described. The current...

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Oxidation of refractory sulfur compounds with molecular oxygen over a Ce-Mo-O...

Green Chemistry International Oxidation of refractory sulfur compounds with molecular oxygen over a Ce-Mo-O catalyst  Green Chem., 2016, Advance Article DOI: 10.1039/C6GC01357K, Paper Yawei Shi,...

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An efficient Passerini tetrazole reaction (PT-3CR)

Green Chemistry International An efficient Passerini tetrazole reaction (PT-3CR) Green Chem., 2016, 18,3718-3721 DOI: 10.1039/C6GC00910G, Communication Ajay L. Chandgude, Alexander Domling A...

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2-Bromo-1,4-benzenedimethanol

(2-bromo-4-hydroxymethylphenyl)methanol;  CAS 89980-92-7;  2-Bromo-1,4-benzenedimethanol; Molecular Formula: C8H9BrO2 Molecular Weight: 217.05986 g/mol (2-Bromo-4-hydroxymethylphenyl)methanol (3). To...

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N-Butylpyrrolidinone as a dipolar aprotic solvent for organic synthesis

N-Butylpyrrolidinone as a dipolar aprotic solvent for organic synthesis Green Chem., 2016, 18,3990-3996 DOI: 10.1039/C6GC00932H, Paper James Sherwood, Helen L. Parker, Kristof Moonen, Thomas J....

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Ring-locking enables selective anhydrosugar synthesis from carbohydrate...

Ring-locking enables selective anhydrosugar synthesis from carbohydrate pyrolysis Green Chem., 2016, Advance Article DOI: 10.1039/C6GC01600F, Paper Li Chen, Jinmo Zhao, Sivaram Pradhan, Bruce E....

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Directed alkynylation of unactivated C(sp3)-H bonds with...

Green Chemistry International Directed alkynylation of unactivated C(sp3)-H bonds with ethynylbenziodoxolones mediated by DTBP Green Chem., 2016, 18,4185-4188 DOI: 10.1039/C6GC01336H, Communication...

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MICONAZOLE NITRATE , Миконазол , ミコナゾール硝酸塩

New Drug Approvals Miconazole            C18H14Cl4N2O    416.13             [22916–47–8] Miconazole Nitrate            C18H14Cl4N2O.HNO3              479.14             [22832–87–7] ミコナゾール硝酸塩...

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Flow Grignard and Lithiation: Screening Tools and Development of Continuous...

Efficient continuous Grignard and lithiation processes were developed to produce one of the key regulatory starting materials for the production of edivoxetine hydrochoride. For the Grignard process,...

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Multicomponent-Multicatalyst Reactions (MC)2R: Efficient Dibenzazepine Synthesis

Multicomponent-Multicatalyst Reactions (MC)2R: Efficient Dibenzazepine Synthesis Jennifer Tsoung, Jane Panteleev, Matthias Tesch, and Mark Lautens Org. Lett. 2014, 16, 110-113. DOI:10.1021/ol4030925 ....

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Visible-light induced oxidative Csp3-H activation of methyl aromatics to...

Green Chemistry International Green Chem., 2016, Advance ArticleDOI: 10.1039/C6GC01880G, Communication Lingling Zhang, Hong Yi, Jue Wang, Aiwen Lei A mild and catalytic oxidative Csp3-H activation of...

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CO2-Catalysed aldol condensation of 5-hydroxymethylfurfural and acetone to a...

Green Chemistry International CO2-Catalysed aldol condensation of 5-hydroxymethylfurfural and acetone to a jet fuel precursor Green Chem., 2016, Advance ArticleDOI: 10.1039/C6GC01697A, Communication...

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Register Today for the ACS Symposium in India on Recent Advances in Drug...

Inaugural ACS Industry Symposium, 11-12 November 2016 in Hyderabad, India Recent Advances in Drug Development Register Today for the ACS Symposium in India on Recent Advances in Drug Development To...

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BMS-852927

New Drug Approvals BMS-852927 CAS 256918-39-4 609.51 MW C29 H28 Cl2 F2 N2 O4 S MF...

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Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through...

Green Chemistry International Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C-H functionalization of pyridine N-oxides Green Chem., 2016, Advance Article DOI:...

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A catalyst-free 1,3-dipolar cycloaddition of C,N-cyclic azomethine imines and...

Green Chemistry International A catalyst-free 1,3-dipolar cycloaddition of C,N-cyclic azomethine imines and 3-nitroindoles: an easy access to five-ring-fused tetrahydroisoquinolines Green Chem., 2016,...

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Simultaneous rapid reaction workup and catalyst recovery

Green Chemistry International Simultaneous rapid reaction workup and catalyst recovery Green Chem., 2016, 18,5769-5772 DOI: 10.1039/C6GC02448C, Communication Zhichao Lu, Zofia Hetman, Gerald B....

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BioAssay Express: models mixing assays & compounds — Cheminformatics 2.0

The latest experimental feature of the BioAssay Express project involves taking all of the curated assays (3500 so far) and their corresponding compounds from PubChem (hundreds of thousands of unique...

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Heck–Matsuda Reaction in Flow

Product 3 was obtained as a mixture of diastereomers (58:42). The NMR data are consistent with literature precedent.20a Major diastereomer: 1H NMR (300 MHz, CDCl3) δ (ppm) 7.25-7.28 (m, 2H), 7.14-7.17...

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