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Die photochemische Tautomerisation eines cyclischen Amidins
Author(s) -
Pfoertner KarlHeinz
Publication year - 1975
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/hlca.19750580323
Subject(s) - chemistry , amidine , tautomer , stereochemistry , molecule , medicinal chemistry , organic chemistry
The cyclic amidine group of the 8‐amino‐2,3,5,5a‐tetrahydro‐5,8a‐propeno‐6 H ,11 H ‐pyrrolo[3,4‐ g ]‐1‐pyrindine ( 2 ) undergoes photochemical tautomerism. In this reaction the dihydropyridine group of a second molecule of 2 acts as a sensitizer.
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