Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Indoleninium salts

The first method is perhaps the most common, and is exemplified by the condensation shown in Scheme 3 of a 2-alkyl heterocyclic quaternary salt or the corresponding methylene base with a 2-hydroxy unsaturated aldehyde grouping (which usually is part of an aromatic ring, as in salicylaldehyde). These intermediates have given a broad assortment of spiropyran classes. The ready availability of 1.2.3.3.-tetraalkyl-3/f-indoleninium salts and salicylaldehydes has led to a large number of spiro-(2i/-l-benzopyran-2,2 -indolines) [this name will be used in preference to the correct T,3 -dihydrospiro(2//-l-bcnzopyran-2,2 -(2 //(-indole)]. A common acronym for this class, BIPS, will be used in this chapter as both singular and plural. [Pg.14]


See other pages where Indoleninium salts is mentioned: [Pg.31]    [Pg.33]    [Pg.385]    [Pg.286]    [Pg.31]    [Pg.33]    [Pg.385]    [Pg.286]    [Pg.125]    [Pg.43]    [Pg.551]   
See also in sourсe #XX -- [ Pg.14 ]




SEARCH



© 2024 chempedia.info