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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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...
View ArticleOxidation 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,...
View ArticleAn efficient Passerini tetrazole reaction (PT-3CR)
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View Article2-Bromo-1,4-benzenedimethanol
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View ArticleN-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....
View ArticleRing-locking enables selective anhydrosugar synthesis from carbohydrate...
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View ArticleMICONAZOLE 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...
View ArticleFlow 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,...
View ArticleMulticomponent-Multicatalyst Reactions (MC)2R: Efficient Dibenzazepine Synthesis
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View ArticleVisible-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...
View ArticleCO2-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...
View ArticleRegister 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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New Drug Approvals BMS-852927 CAS 256918-39-4 609.51 MW C29 H28 Cl2 F2 N2 O4 S MF...
View ArticleSolvent- 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:...
View ArticleA 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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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....
View ArticleBioAssay 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...
View ArticleHeck–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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