Sorocein I, a new Diels-Alder type adduct from Sorocea ilicifolia.

  title={Sorocein I, a new Diels-Alder type adduct from Sorocea ilicifolia.},
  author={Francimar Ferrari and Franco Delle Monache},
  volume={72 3},
5 Citations

Diels-Alder Type Adducts from Hairy Root Cultures of Morus macroura

− Three Diels-Alder type adducts, guangsangon E ( 1 ), chalcomoracin ( 2 ) and sorocein I ( 3 ) were isolated from hairy root cultures of Morus macroura . The structures of the isolated compounds ( 1

Mulberry Diels–Alder-type adducts: isolation, structure, bioactivity, and synthesis

Mulberry Diels–Alder-type adducts (MDAAs) are unique phenolic natural products biosynthetically derived from the intermolecular [4 + 2]-cycloaddition of dienophiles (mainly chalcones) and

Enantioselective Total Syntheses of Kuwanon X, Kuwanon Y, and Kuwanol A.

The first enantioselective total syntheses of (-)-kuwanon X, (+)-kuwanon Y, and (+)-kuwanol A have been accomplished by using asymmetric Diels-Alder cycloaddition promoted by chiral VANOL or



Three New Diels-Alder Type Adducts from the Roots of Sorocea bonplandii Baillon

Three new ketalized Diels-Alder type adducts named soroceal (1), sorocein A (2), sorocein B (3), were isolated from the methanolic extract of the roots of Sorocea bonplandii. The structures were

Structures of three new 2-arylbenzofuran derivatives from the chinese crude drug "Sang-Bai-Pi" (morus root bark).

Three new 2-arylbenzofuran derivatives named mulberrofurans K, N, and O were isolated from the extract of the Chinese crude drug "Sang-Bai-Pi" (Japanese name "Sohakuhi"), the root bark of Morus sp.