91704-75-5Relevant articles and documents
An asymmetric dihydroxylation route to (S)-oxybutynin
Gupta, Priti,Fernandes, Rodney A.,Kumar, Pradeep
, p. 4231 - 4232 (2003)
An asymmetric synthesis of (S)-oxybutynin 1 is described using the Sharpless asymmetric dihydroxylation of α-cyclohexylstyrene as the key step.
Visible light-promoted dihydroxylation of styrenes with water and dioxygen
Yang, Bo,Lu, Zhan
, p. 12634 - 12637 (2017/12/02)
An efficient visible light promoted metal-free dihydroxylation of styrenes with water and dioxygen has been developed for the construction of vicinal alcohols. The protocol was operationally simple with a broad substrate scope. The mechanistic studies demonstrated that one of the hydroxyl groups came from water and the other one came from molecular oxygen. Additionally, the β-alkyoxy alcohols could also be obtained using a similar strategy.
Ligand-dependent reversal of facial selectivity in the asymmetric dihydroxylation
Vanhessche, Koen P. M.,Sharpless, K. Barry
, p. 7978 - 7979 (2007/10/03)
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