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A Mn(III)‐mediated radical cyclization reaction of o‐vinyl arylisocyanides and arylboronic acids or diphenylphosphine oxides to access various 2‐funtionalized quinolines under mild conditions was developed. With the introduction of radical stabilizing substituents (e.g. aryl and methyl group) on vinyl group, this reaction provides a regiospecific 6‐endo‐trig radical cyclization of o‐vinyl arylisocyanides, giving a number of structurally unique and biologically potential 2‐functionalized quinoline derivatives.
The front cover picture, designed by Xiaoyu Han and co‐workers, illustrates a highly diastereo‐ and enantioselective organocatalytic Mannich reaction of isatin‐derived N‐Boc‐imines with homophthalic anhydrides, which allows the direct synthesis of a wide range of enantiomerically enriched oxindole‐derived α‐aryl‐β‐amino acid derivatives with two adjacent chiral carbon centers.
Financial Express (India) 12/08/2019 03:17
"Paper industry is going through the transformation phase and now the paper industry uses less power and water due to technological changes. Cost of production of recycled paper is at least 30 to 40 per cent cheaper depending upon the location than the recycled plastic," J P Narain, VP, Indian Paper & Manufacturers Association and CEO of Century Paper said.

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