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DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 30 Yrs Exp. in the feld of Organic Chemistry. Serving chemists around the world. Helping them with websites on Chemistry.Millions of hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution
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Monday, 16 June 2014

C–C Coupling Repertoire Grows ... Organic Synthesis: Reaction eases addition of chiral carbon centers to aryl groups

 

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REVIVAL
This new reaction combines chiral secondary and tertiary boronic esters (left) with lithiated aryls to form intermediates that rearrange upon electrophile addition, yielding aryl-alkyl coupling products.
The revival of a nearly 50-year-old technique for forming carbon-carbon bonds may help ease the synthesis of aryl derivatives, such as drug candidates.
Varinder K. Aggarwal and coworkers at the University of Bristol, in England, have taken a venerable but neglected synthesis called Zweifel olefination and made it new again (Nat. Chem. 2014, DOI: 10.1038/nchem.1971).

C–C Coupling Repertoire Grows

Organic Synthesis: Reaction eases addition of chiral carbon centers to aryl groups
 http://cen.acs.org/articles/92/i24/CC-Coupling-Repertoire-Grows.html
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A TWO-STEP TANDEM REACTION TO PREPARE HYDROXAMIC ACIDS DIRECTLY FROM ALCOHOLS | ORGANIC CHEMISTRY SELECT

A TWO-STEP TANDEM REACTION TO PREPARE HYDROXAMIC ACIDS DIRECTLY FROM ALCOHOLS | ORGANIC CHEMISTRY SELECT:



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Wednesday, 11 June 2014

Boronic Acid Catalyzed Annulation of a Pyran Ring



Boronic Acid Catalyzed Annulation of a Pyran Ring

A route to oxygenated pyrano[3,2-a]- and pyrano[2,3-a]carbazole alkaloids
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Amine Methylation Made Easy



Amine Methylation Made Easy

A mild and catalytic methylation of amines with formic acid
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Friday, 30 May 2014

Visible-light-induced photocatalytic formyloxylation reactions of 3-bromooxindoles with water and DMF: the scope and mechanism

Green Chem., 2014, Advance Article
DOI: 10.1039/C4GC00647J, Paper
You-Quan Zou, Wei Guo, Feng-Lei Liu, Liang-Qiu Lu, Jia-Rong Chen, Wen-Jing Xiao
A highly efficient visible light induced formyloxylation reaction of 3-bromooxindoles was disclosed. Results of labeling experiments indicated that H2O and DMF were incorporated into the terminal 3-formyloxyoxindoles.
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The formyloxylation reaction of 3-bromooxindoles with water and N,N-dimethylformamide (DMF) has been developed in the presence of the photoredox catalyst fac-Ir(ppy)3 under irradiation of visible light at ambient temperature. The reaction provides a straightforward approach to pharmaceutically and synthetically useful 3-formyloxyoxindoles in high yields. The mechanism of this transformation was investigated by fluorescence quenching experiments, “on–off” switching of the light source, labeling experiments, mass spectral analyses and in situ IR experiments.




ANTHONY MELVIN CRASTO
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amcrasto@gmail.com
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