130129-15-6Relevant articles and documents
Hydroxyl-directed cyclopropanation of Z-allylsilanes
Mohr, Peter
, p. 7221 - 7224 (1995)
Z-5-Hydroxy-alk-2-enyl-silanes of general structure 1 are cyclopropanated by an excess of CH2l2 / Et2Zn in good yield and excellent stereoselectivity. Ensuing protodesilylation, however, lacks efficient regiocontrol and affords syn-products 5 in modest yield but high stereochemical purity.
New asymmetric synthesis of a pheromone component of the shield bug Cantao Parentum
Mineeva
, p. 398 - 405 (2014/06/09)
A novel procedure has been developed for the synthesis of (2S,4R,6R,8S)-2,4,8-trimethyl-1,7-dioxaspiro[5.5]undecane, a pheromone component of the shield bug Cantao Parentum, through intermediate cyclopropanol derivatives in the key stages of carbon chain
A CONVERGENT ENANTIOCONTROLLED ROUTE TO MEVALONOLACTONE AND VITAMIN E FROM (S)-O-BENZYLGLYCIDOL
Takano, Seiichi,Shimazaki, Youichi,Iwabuchi, Yoshiharu,Ogasawara, Kunio
, p. 3619 - 3622 (2007/10/02)
A convergent enantiocontrolled route to (+) and (-)-mevalonolactones and vitamin E has been developed using (S)-O-benzylglycidol as the sole chiral block.
Enantio-and Stereo-controlled Construction of Tertiary and Quaternary Carbon Centers Using Chiral O-Benzylglycidol as Template
Takano, Seiichi,Shimazaki, Youichi,Moriya, Minoru,Ogasawara, Kunio
, p. 1177 - 1180 (2007/10/02)
An efficient method for the enantio- and stereo-controlled construction of tertiary and quaternary carbon centers in a highly functionalized system has been developed using chiral O-benzylglycidol as template.