01626nas a2200265   4500008004100000022001400041245016100055210006900216260010600285300001400391490000700405520058200412653001400994653002001008653001201028653001801040100003101058700002401089700002301113700002601136700002401162700002401186700002501210856012501235       2011                        eng d  a0040-403900aOne-step synthesis of 4-alkyl-3-aryl-2,6-dicyanoanilines and their use in the synthesis of highly functionalized 2,3,5,6,7-and 2,3,4,5,7-substituted indoles0 aOnestep synthesis of 4alkyl3aryl26dicyanoanilines and their use   aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcOCT  a5491-54930 v523 a<p>A three-component, one-step method for the synthesis of 4-alkyl-3-aryl-2,6-dicyanoanilines involving reaction of alkyl aldehyde, malononitrile and aryl aldehyde in presence of morpholine is reported. Highly functionalized 2,3,5,6,7- and 2,3,4,5,7-substituted indoles were prepared from these dicyanoanilines by reaction with ethyl bromoacetate. These substituted dicyanoanilines and indoles have a potential to be converted into various other compounds taking advantage of various functional groups present in these molecules. (C) 2011 Elsevier Ltd. All rights reserved.</p>10aaldehydes10aDicyanoanilines10aindoles10aMalononitrile1 aSawargave, Sangmeshwer, P.1 aKudale, Ananada, S.1 aDeore, Jaydeep, V.1 aBhosale, Dattatry, S.1 aDivse, Jaisingh, M.1 aChavan, Subhash, P.1 aBorate, Hanumant, B.  uhttps://library.ncl.res.in/content/one-step-synthesis-4-alkyl-3-aryl-26-dicyanoanilines-and-their-use-synthesis-highly-001437nas a2200277   4500008004100000022001400041245009800055210006900153260010600222300001400328490000700342520042300349653002300772653002200795653001600817653001900833653001800852100002500870700002500895700002400920700002400944700002700968700002200995700002301017856011901040       2013                        eng d  a0040-403900aOne-step method for the synthesis of aryl olefins from aryl aldehydes and aliphatic aldehydes0 aOnestep method for the synthesis of aryl olefins from aryl aldeh  aTHE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLANDbPERGAMON-ELSEVIER SCIENCE LTDcMAR  a1528-15300 v543 a<p>A conceptually new one-step reaction affording unexpected aryl olefinic product from aromatic aldehyde, aliphatic aldehyde and malononitrile in the presence of acetic acid-ammonium acetate under mild reaction conditions without using any metal catalyst is reported. This novel reaction was used to prepare a number of substituted aryl olefins including new molecules. (c) 2013 Elsevier Ltd. All rights reserved.</p>10aAliphatic aldehyde10aAromatic aldehyde10aAryl olefin10aDicyanoaniline10aMalononitrile1 aBorate, Hanumant, B.1 aGaikwad, Supriya, H.1 aKudale, Ananada, S.1 aChavan, Subhash, P.1 aPharande, Shrikant, G.1 aWagh, Vitthal, D.1 aSawant, Vikram, S.  uhttps://library.ncl.res.in/content/one-step-method-synthesis-aryl-olefins-aryl-aldehydes-and-aliphatic-aldehydes-0