170711-93-0Relevant academic research and scientific papers
The absolute stereochemistry of a diterpene from Ballota aucheri
Gray, Christopher A.,Rivett, Douglas E.A.,Davies-Coleman, Michael T.
, p. 409 - 413 (2003)
The semi-synthetic transformation of hispanolone, isolated from Ballota africana, into βp-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one has established an ent-labdane absolute stereochemistry for a diterpene metabolite originally isolated from B. aucheri.
Transformations of hispanolone. Novel Michael adducts with in planta activity against rice blast
Van Wyk, Albert W.W.,Gray, Christopher A.,Keyzers, Robert A.,Rivett, Douglas E.A.,Caira, Mino R.,Nader, Bassam S.,Davis, George E.,Werk, Todd L.,Davies-Coleman, Michael T.
, p. 8493 - 8498 (2005)
Two novel Michael adducts 9α-cyano-15,16-epoxy-7β-hydroxylabda- 13(16),14-dien-6-one (2) and 9α-cyano-15,16-epoxy-7-hydroxylabda-7,13(16), 14-trien-6-one (3) and the reduction product of 2, 9α-cyano-15,16-epoxy- 6β,7β-dihydroxylabda-13(16),14-diene (4), w
Synthesis of sibiricinone A, sibiricinone B and leoheterin
Marcos,Casta?eda,Basabe,Díez,Urones
, p. 10860 - 10866 (2008/12/23)
Two labdenolides, sibiricinone A and sibericinone B, and a furo-labdane leoheterin have been synthesized from sclareol, for the first time, establishing in this manner the absolute configuration for these compounds.
