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Pyrrole-singlet oxygen reactions leading to α,α′-bipyrroles. Synthesis of prodigiosin and analogs

✍ Scribed by Harry H. Wasserman; Anders K. Petersen; Mingde Xia; Jianji Wang


Book ID
104262319
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
171 KB
Volume
40
Category
Article
ISSN
0040-4039

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✦ Synopsis


Reaction of the ten-butyl ester of 3-methoxy-2-pyrrolecarboxylic acid with singlet oxygen yields a hydroperoxide intermediate which undergoes coupling with pyrroles to yield precursors of prodigiosin and ring A analogs, readily convertible to the corresponding tripyrromethenes.


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