N Diedrichs, JP Ragot, K Thede
Index: Diedrichs, Nicole; Ragot, Jacques P.; Thede, Kai European Journal of Organic Chemistry, 2005 , # 9 p. 1731 - 1735
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Citation Number: 16
Abstract Rocaglaols are natural products exhibiting a range of biological activities. A new synthetic method for the α-arylation of ketones allows for the synthesis of previously inaccessible rocaglaol derivatives. The key sequence consists of a previously unreported Suzuki type reaction using brominated silyl enol ethers as substrates followed by deprotection of the arylated silyl enol ethers.(© Wiley-VCH Verlag GmbH & Co. KGaA, ...
4225-35-8
4,6-dimethoxy-1...
106-38-7
4-Bromotoluene
~49%
857062-50-1
4,6-dimethoxy-2...
104-92-7
4-Bromoanisole
~34%
117828-33-8