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Published in 2018 at "Chirality"
DOI: 10.1002/chir.22867
Abstract: (R)-Metacycloprodigiosin can exist in three different tautomeric forms, each with hydrogens at C9' and C12 in syn or anti orientation. With the addition of HCl, this structural diversity reduces to syn-(R)-metacycloprodigiosin-HCl (1a) and anti-(R)-metacycloprodigiosin-HCl (1b),…
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Keywords:
properties structure;
hcl chiroptical;
metacycloprodigiosin hcl;
metacycloprodigiosin ... See more keywords