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10.1021/ja5046296 http://scihub22266oqcxt.onion/10.1021/ja5046296 C4073881!4073881!24926794     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Am+Chem+Soc 2014 ; 136 (25): 8915-8 Nephropedia Template TP {{tp|p=24926794|t=2014. Lewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoamination of Olefins |pdf=|usr=}}{{24926794}} gab.com Text Lewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoamination of Olefins JO: J Am Chem Soc http://www.kidney.de/pget.php?&tw=1&pmid=24926794 #FOAvip A method for the enantioselective, intramolecular sulfenoamination of various olefins has been developed using a chiral BINAM-based selenophosphoramide, Lewis base catalyst. Terminal and trans disubstituted alkenes afforded pyrrolidines, piperidines, and azepanes in high yields and high enantiomeric ratios via enantioselective formation and subsequent stereospecific capture of the thiiranium intermediate with the pendant tosyl-protected amine. Twit Text FOAVip Lewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoamination of Olefins ????J Am Chem Soc http://www.kidney.de/pget.php?&tw=1&pmid=24926794 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24926794 #FOAvip English Wikipedia <ref>{{Cite pmid|24926794}}</ref> Lewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoamination of Olefins #MMPMID24926794 Denmark SE; Chi HM J Am Chem Soc 2014[Jun]; 136 (25): 8915-8 PMID24926794show ga A method for the enantioselective, intramolecular sulfenoamination of various olefins has been developed using a chiral BINAM-based selenophosphoramide, Lewis base catalyst. Terminal and trans disubstituted alkenes afforded pyrrolidines, piperidines, and azepanes in high yields and high enantiomeric ratios via enantioselective formation and subsequent stereospecific capture of the thiiranium intermediate with the pendant tosyl-protected amine. äLewis Base Catalyzed, Enantioselective, Intramolecular Sulfenoaminatio(epmc).pdf DeepDyve Pubget Overpricing