37556-09-5Relevant articles and documents
Reversible ON/OFF nanoswitch for organocatalysis: Mimicking the locking and unlocking operation of CaMKII
Schmittel, Michael,De, Soumen,Pramanik, Susnata
supporting information; experimental part, p. 3832 - 3836 (2012/06/15)
Flip a switch: A nanoswitch uses chemical inputs to turn an organocatalytic Knoevenagel reaction on and off (see scheme: R=reactant, P=product). To stop catalysis the chemical input (pink and green) wraps around the inhibitory segment of the nanoswitch to
Synthesis of 3-Phenoxybenzyl 3-Alkyl-3-phenyl-/p-substituted phenyl and 3-Phenoxybenzyl 2-Alkyl-3-phenyl-/p-substituted phenylpropionates
Kelkar, S. V.,Joshi, G. S.,Kulkarni, G. H.,Mitra, R. B.
, p. 68 - 70 (2007/10/02)
Some 3-phenoxybenzyl 3-alkyl-3-phenyl-/p-substituted phenylpropionates (VII, XI, XV, XIX, XXIII, XXVII) which resemble structurally the 1,2-secopyrethroids, have been prepared employing simple reactions like alkylation, decarbethoxylation and transesterification.The synthesis of 3-phenoxybenzyl 2-alkyl-3-phenyl-/p-substituted phenyl-propionates (XXXI, XXXII, XXXIII, and XXXVI) bearing close structural resemblance to 2,3-secopyrethroids has also been described.