937035-21-7Relevant articles and documents
Biosynthesis of Stereoisomers of Dill Ether and Wine Lactone by Pleurotus sapidus
Trapp, Tobias,Kirchner, Tabea,Birk, Florian,Fraatz, Marco Alexander,Zorn, Holger
, p. 13400 - 13411 (2019)
The white-rot fungus Pleurotus sapidus (PSA) biosynthesizes the bicyclic monoterpenoids 3,6-dimethyl-2,3,3a,4,5,7a-hexahydrobenzofuran (dill ether) (1) and 3,6-dimethyl-3a,4,5,7a-tetrahydro-1-benzofuran-2(3H)-one (wine lactone) (2). Submerged cultures gro
A chemoenzymatic, preparative synthesis of the isomeric forms of p-menth-1-en-9-ol: Application to the synthesis of the isomeric forms of the cooling agent 1-hydroxy-2,9-cineole
Serra, Stefano,Fuganti, Claudio,Gatti, Francesco G.
experimental part, p. 1031 - 1037 (2009/04/05)
A preparative-scale synthesis of the four p-menth-1-en-9-ol isomers 2a-5a has been achieved by means of two chemoenzymatic processes. Both synthetic pathways start from the enantiomeric forms of limonene that are converted into p-mentha-1,8-dien-9-al isomers 12 and 15. The baker's yeast mediated reduction of the latter aldehydes afforded compounds 3a and 5a, respectively, with very high enantioselectivity. Moreover, chemical reduction of 12 and 15 gives the mixtures of enantiopure diastereoisomers 2a/3a and 4a/5a, respectively. PPL (Porcine pancreas lipase) mediated resolution of the latter mixtures followed by fractionating crystallization of derivatives 2b-5b allowed the enantio- and diastereoisomerically pure alcohols 2a-5a to be obtained. Compounds 2a-5a have then been used as starting materials for the preparation of four isomers of the cooling agent 1-hydroxy-2,9-cineole (6-9). Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
REVISIONS OF THE ABSOLUTE CONFIGURATIONS OF C-8 METHYL GROUPS IN DEHYDROIRIDODIOL, NEONEPETALACTONE, AND MATATABIETHER FROM ACTINIDIA POLYGAMA MIQ
Sakai, Tsutomu,Nakajima, Kimiko,Yoshihara, Kazuo,Sakan, Takeo,Isoe, Sachihiko
, p. 3115 - 3119 (2007/10/02)
The absolute configurations of C-8 Me groups in dehydro-iridodiol, neonepetalactone, and matatabiether isolated from the cat- and lacewing-attracting plant Actinidia polygama Miq. were revised to the S configurations on the basis of chemical transformatio