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Investigations on the Reactivity of Fascaplysin, Part I, Aromatic Electrophilic Substitutions Occur at Position 9
Author(s) -
Fretz Heinz,
UcciStoll Katharina,
Hug Paul,
Schoepfer Joseph,
Lang Marc
Publication year - 2000
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/1522-2675(20001108)83:11<3064::aid-hlca3064>3.0.co;2-p
Subject(s) - chemistry , electrophile , reactivity (psychology) , organic chemistry , position (finance) , electrophilic substitution , electrophilic aromatic substitution , combinatorial chemistry , catalysis , medicine , alternative medicine , pathology , finance , economics
Electrophilic aromatic substitutions, such as halogenation and sulfonation, occur primarily para to the indole N‐atom at C(9) of the unique 12 H ‐pyrido[1,2‐ a: 3,4‐ b ′]diindole ring system of fascaplysin.