152821-16-4Relevant articles and documents
Tandem molybdenum catalyzed hydrosilylations: An expedient synthesis of β-aryl aldehydes
Frost, Christopher G.,Hartley, Benjamin C.
, p. 4259 - 4261 (2007)
The synthesis of β-aryl aldehydes utilizing a tandem molybdenum catalyzed hydrosilylation is described. This new functional group interconversion provides an efficient method for the two-carbon homologation of aryl aldehydes.
Synthesis and biological evaluation of arylidene analogues of Meldrum's acid as a new class of antimalarial and antioxidant agents
Sandhu, Harmeet S.,Sapra, Sameer,Gupta, Mukesh,Nepali, Kunal,Gautam, Raju,Yadav, Sunil,Kumar, Raj,Jachak, Sanjay M.,Chugh, Manoj,Gupta, Manish K.,Suri, Om P.,Dhar
experimental part, p. 5626 - 5633 (2010/09/11)
A series of arylidene analogues of Meldrum's acid were synthesized and evaluated for in vitro antimalarial and antioxidant activities for the first time. The influence of various physico-chemical parameters such as dielectric constant (), donor number (DN
An efficient preparation of coumarins
Rouessac,Leclerc
, p. 2709 - 2715 (2007/10/02)
o-Methoxyaryl-aldehydes (or -ketones) react in solid-phase with Meldrum's acid under mild conditions, to give benzylidene derivatives which are cyclized in high yield, with cold sulfuric acid to substituted 3-carboxycoumarins. Thermal decarboxylation, spe
