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10.1007/s00706-020-02584-8 http://scihub22266oqcxt.onion/10.1007/s00706-020-02584-8 C7186117!7186117!32346184     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 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Monatsh+Chem 2020 ; 151 (4): 605-10 Nephropedia Template TP {{tp|p=32346184|t=2020. Assembling the prenylneoflavone system through a Pechmann condensation/Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis sequence |pdf=|usr=}}{{32346184}} gab.com Text Assembling the prenylneoflavone system through a Pechmann condensation/Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis sequence JO: Monatsh Chem http://www.kidney.de/pget.php?&tw=1&pmid=32346184 #FOAvip Abstract: The multistep synthesis of a prenylneoflavone through a sequence of the Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis reaction has been accomplished in 5% yield over six steps starting from commercially available 3-methoxyacetophenone. The sequence is shown to be compatible with a Pechmann condensation which proved to be a robust and cost-effective method for the assembling of the ?-pyrone core. The results open doors to a general approach to the prenylneoflavone system starting from phenol and acetophenone derivatives. Graphic abstract: Electronic supplementary material: The online version of this article (10.1007/s00706-020-02584-8) contains supplementary material, which is available to authorized users. Twit Text FOAVip Assembling the prenylneoflavone system through a Pechmann condensation/Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis sequence ????Monatsh Chem http://www.kidney.de/pget.php?&tw=1&pmid=32346184 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32346184 #FOAvip English Wikipedia <ref>{{Cite pmid|32346184}}</ref> Assembling the prenylneoflavone system through a Pechmann condensation/Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis sequence #MMPMID32346184 Lozinski OA; Bistodeau J; Bennetau-Pelissero C; Khilya VP; Shinkaruk S Monatsh Chem 2020[]; 151 (4): 605-10 PMID32346184show ga Abstract: The multistep synthesis of a prenylneoflavone through a sequence of the Mitsunobu reaction/Claisen rearrangement/olefin cross-metathesis reaction has been accomplished in 5% yield over six steps starting from commercially available 3-methoxyacetophenone. The sequence is shown to be compatible with a Pechmann condensation which proved to be a robust and cost-effective method for the assembling of the ?-pyrone core. The results open doors to a general approach to the prenylneoflavone system starting from phenol and acetophenone derivatives. Graphic abstract: Electronic supplementary material: The online version of this article (10.1007/s00706-020-02584-8) contains supplementary material, which is available to authorized users. äAssembling the prenylneoflavone system through a Pechmann condensation(epmc).pdf DeepDyve Pubget Overpricing