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10.1016/j.tet.2016.11.016 http://scihub22266oqcxt.onion/10.1016/j.tet.2016.11.016 C5603183!5603183!28943665     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Tetrahedron 2017 ; 73 (29): 4206-13 Nephropedia Template TP {{tp|p=28943665|t=2017. The intramolecular click reaction using ?carbocontiguous? precursors |pdf=|usr=}}{{28943665}} gab.com Text The intramolecular click reaction using carbocontiguous precursors JO: Tetrahedron http://www.kidney.de/pget.php?&tw=1&pmid=28943665 #FOAvip The synthesis and utilization of all carbon-chain ?carbocontiguous? azidoalkynyl precursors for an intramolecular click reaction is described. The substrates contain both azidoalkyl and ethynylmethyl groups which are conjoined by a 2-(phenylsulfonylmethyl)-4,5-diphenyloxazole lynchpin and are suitably disposed for ring closure. On promotion by copper salts, a number of cyclic click products having the 1,4-disubstituted endo-fused triazole component and the 4,5-diphenyloxazole component are obtained. In one case, removal of the phenylsulfonylmethyl group from the substrate prior to cyclization gave the 1,5-disubstituted exo-fused triazole. The utilization of CuSO4/sodium ascorbate system appears to be the optimal conditions for closure/cyclization and afforded the cyclized products in yields of 84-95%. Twit Text FOAVip The intramolecular click reaction using carbocontiguous precursors ????Tetrahedron http://www.kidney.de/pget.php?&tw=1&pmid=28943665 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28943665 #FOAvip English Wikipedia <ref>{{Cite pmid|28943665}}</ref> The intramolecular click reaction using ?carbocontiguous? precursors #MMPMID28943665 Patil PC; Luzzio FA Tetrahedron 2017[Jul]; 73 (29): 4206-13 PMID28943665show ga The synthesis and utilization of all carbon-chain ?carbocontiguous? azidoalkynyl precursors for an intramolecular click reaction is described. The substrates contain both azidoalkyl and ethynylmethyl groups which are conjoined by a 2-(phenylsulfonylmethyl)-4,5-diphenyloxazole lynchpin and are suitably disposed for ring closure. On promotion by copper salts, a number of cyclic click products having the 1,4-disubstituted endo-fused triazole component and the 4,5-diphenyloxazole component are obtained. In one case, removal of the phenylsulfonylmethyl group from the substrate prior to cyclization gave the 1,5-disubstituted exo-fused triazole. The utilization of CuSO4/sodium ascorbate system appears to be the optimal conditions for closure/cyclization and afforded the cyclized products in yields of 84-95%. äThe intramolecular click reaction using ?carbocontiguous? precursors (epmc).pdf DeepDyve Pubget Overpricing