42123-27-3Relevant articles and documents
Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest
Liu, Yixi,Young, Kelly,Rakotondraibe, L. Harinantenaina,Brodie, Peggy J.,Wiley, Jessica D.,Cassera, Maria B.,Callmander, Martin W.,Rakotondrajaona,Rakotobe, Etienne,Rasamison, Vincent E.,Tendyke, Karen,Shen, Yongchun,Kingston, David G. I.
, p. 1543 - 1547 (2015)
The two new lignans 3α-O-(β-d-glucopyranosyl)desoxypodophyllotoxin (1) and 4-O-(β-d-glucopyranosyl)dehydropodophyllotoxin (2) were isolated from Cleistanthus boivinianus, together with the known lignans deoxypicropodophyllotoxin (3), (±)-β-apopicropodophy
A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells
Kamal, Ahmed,Damayanthi
, p. 657 - 662 (2007/10/03)
The biotransformation of aryltetralin lignans to arylnaphthalene lignans in presence of yeast is described. Podophyllotoxone, an oxidation product of podophyllotoxin on incubation with yeast from different sources produced dehydropodophyllotoxin, an important representative of arylnaphthalene lignans.
Efficient Syntheses of 1-Arylnaphthalene Lignan Lactones and Related Compounds from Cyanohydrins
Ogiku, Tsuyoshi,Yoshida, Shin-ichi,Ohmizu, Hiroshi,Iwasaki, Tameo
, p. 4585 - 4590 (2007/10/02)
1-Arylnaphthalene lignan lactones were synthesized in good yields from O-(tert-butyldimethylsilyl)cyanohydrins in two steps based on a conjugate addition-aldol reaction, followed by acid-catalyzed closure to form the naphthalene ring. 4-Hydroxy-1-arylnaph