Definition of Di-pimethane rearrangement

1. Noun. A photochemical reaction of a molecular entity comprising two p-systems, separated by a saturated carbon atom (a 1,4-diene or an allyl-substituted aromatic analog), to form an ene- (or aryl-) substituted cyclopropane. The rearrangement formally amounts to a 1,2 shift of one ene group (in the diene) or the aryl group (in the allyl-aromatic analog) and ‘bond formation’ between the lateral carbons of the non-migrating moiety. ¹

¹ Source: wiktionary.com

Lexicographical Neighbors of Di-pimethane Rearrangement

dhrupad
dhurna
dhurnas
dhurra
dhurras
dhurrie
dhurries
dhuti
dhutis
dhyana
di(2-chloroethyl)sulfide
di-
di-amelia
di-iodotyrosine
di-pimethane rearrangement (current term)
di di mau
di ex machina
di ex machinis
dia-
diabase
diabases
diabasic
diabaterial
diabatic
diabatically
diabatization
diabesity
diabetes
diabetes and fibre

Other Resources:

Search for Di-pimethane rearrangement on Dictionary.com!Search for Di-pimethane rearrangement on Thesaurus.com!Search for Di-pimethane rearrangement on Google!Search for Di-pimethane rearrangement on Wikipedia!

Search