111465-42-0Relevant articles and documents
Talaromycins: Applications of Homonuclear Spin Correlation Maps to Structure Assignements
Lynn, David G.,Phillips, Nancy J.,Hutton, William C.,Shabanowitz, Jeffrey,Fennell, D. I.,Cole, R. J.
, p. 7319 - 7322 (1982)
-
Enantioselective Total Synthesis of the Mycotoxin (-)-Talaromycin B by a Hetero Diels-Alder Reaction
Tietze, Lutz F.,Schneider, Christoph
, p. 2476 - 2481 (2007/10/02)
(-)-Talaromycin B was formed in an overall yield of 5 percent in nine steps via a hetero Diels-Alder reaction of the exocyclic vinyl ether 3 and methyl O-benzoyldiformylacetate (4) as the key transformation.The enantiomerically pure vinyl ether 3 was prep
SYNTHESIS OF (-)-TALAROMYCINS A AND B
Mori, Kenji,Ikunaka, Masaya
, p. 45 - 58 (2007/10/02)
Highly enantiomerically pure (-)-talaromycins A and B undecane> were synthesized starting from chiral building blocks of microbial origin.