Journal of the Chemical Society. Chemical communications p. 1313 - 1315 (1987)
Update date:2022-08-03
Topics:
Hawker, Craig J.
Stark, W. Marshall
Battersby, Alan R.
A di(pyrrolylmethyl)-2H-pyrrole has been synthesised and its ready acid-catalysed rearrangement shows that one of the two possible modes of cleavage is preferred; this mode corresponds to that required for the formation of uroporphyrinogen-III from the putative spiro intermediate.
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