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cycloaddition
κυκλοπροσθήκη
Ultimo aggiornamento 2015-07-09
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a strong driving force for the [4+2] cycloaddition of such species is a result of the establishment (or reestablishment) of aromaticity.
Μια ισχυρή κατευθυντήρια δύναμη για την [4+2] κυκλοπροσθήκη τέτοιων ειδών είναι αποτέλεσμα της δημιουργίας (ή επαναδημιουργίας) της αρωματικότητας.
Ultimo aggiornamento 2016-03-03
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==see also==* inverse electron-demand diels–alder reaction* intramolecular diels–alder cycloaddition* imine diels–alder reaction==references====bibliography==* isbn 0387448993 (part a), isbn 0387683542 (part b)==external links==* asymmetric hetero-diels–alder reactions* semi-empirical calculations of the diels–alder reaction.
==Βιβλιογραφία==* isbn 0387448993 (part a), isbn 0387683542 (part b)* asymmetric hetero-diels–alder reactions* semi-empirical calculations of the diels–alder reaction.
Ultimo aggiornamento 2016-03-03
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