- Biomimetic Synthesis of Meroterpenoids by Dearomatization-Driven Polycyclization
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A biomimetic route to farnesyl pyrophosphate and dimethyl orsellinic acid (DMOA)-derived meroterpenoid scaffolds has yet to be reported despite great interest from the chemistry and biomedical research communities. A concise synthetic route with the poten
- Powers, Zachary,Scharf, Adam,Cheng, Andrea,Yang, Feng,Himmelbauer, Martin,Mitsuhashi, Takaaki,Barra, Lena,Taniguchi, Yoshimasa,Kikuchi, Takashi,Fujita, Makoto,Abe, Ikuro,Porco, John A.
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supporting information
p. 16141 - 16146
(2019/11/03)
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- 206. Synthese des pseudocyphellarines A et B, deux depsides du lichen Pseudocyphellaria endochrysea
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The total synthesis of the depsides pseudocyphellarin A ( = 3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 3-formyl-2,4-dihydroxy-5,6-dimethylbenzoate; 11) and pseudocyphellarin B (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 2,4-dihydroxy-3-hydro
- Pulgarin, Cesar,Gunzinger, Jan,Tabacchi, Raffaele
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p. 1948 - 1951
(2007/10/02)
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- Synthesis of the Lichen Depsides Pseudocyphellarin A and B
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The total synthesis of the fully substituted lichen depsides, pseudocyphellarin A (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylphenyl 3-formyl-2,4-dihydroxy-5,6-dimethylbenzoate) (1) and pseudocyphellarin B (3-hydroxy-4-methoxycarbonyl-2,5,6-trimethylpheny
- Elix, John A.,Lajide, Labunmi
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p. 2153 - 2157
(2007/10/02)
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- PSEUDOCYPHELLARINS A AND B, TWO FULLY SUBSTITUTED DEPSIDES FROM THE LICHEN PSEUDOCYPHELLARIA ENDOCHRYSEA
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The structures of two fully substituted depsides, pseudocyphellarins A and B, have been elucidated by spectroscopic and chemical methods from the lichen Pseudocyphellaria endochrysea. - Keywords: Pseudocyphellaria endochrysea; Stictaceae; lichen; pseudocy
- Huneck, Siegfried
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p. 431 - 434
(2007/10/02)
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