Metal free synthesis of homoallylic alcohols promoted by ultrasound.

[1]  P. Menezes,et al.  Allylation of aldehydes with potassium allyltrifluoroborate catalyzed by Amberlyst A-15 , 2013 .

[2]  R. Longo,et al.  Allylation of Aldehydes with Potassium Allyltrifluoroborate Catalyzed by Lanthanide‐Based Metal‐Organic Framework. , 2013 .

[3]  I. Malvestiti,et al.  Stereoselective Synthesis of Pseudoglycosides Catalyzed by TeCl4 under Mild Conditions. , 2013 .

[4]  P. Menezes,et al.  Allylation of Functionalized Aldehydes by Potassium Allyltrifluoroborate Catalyzed by 18-Crown-6 in Aqueous Media , 2012, Molecules.

[5]  Xiaohua Xu,et al.  Zinc or indium-mediated Barbier-type allylation of aldehydes with 3-bromomethyl-5H-furan-2-one in aqueous media: an efficient synthesis method for α-methylene-γ-butyrolactone. , 2012, Organic & biomolecular chemistry.

[6]  Thierry Ollevier,et al.  Bismuth triflate-catalyzed asymmetric allylation of aromatic aldehydes. , 2012, Chemistry.

[7]  M. Yus,et al.  Catalytic Enantioselective Allylation of Carbonyl Compounds and Imines , 2012 .

[8]  G. Palmisano,et al.  Power Ultrasound in Metal-Assisted Synthesis: From Classical Barbier-like Reactions to Click Chemistry , 2011 .

[9]  P. Phukan,et al.  Ti-Exchanged ZSM-5 as Heterogeneous Catalyst for Allylation of Aldehydes with Allyltributylstannane. , 2011 .

[10]  B. List,et al.  Palladium/Brønsted Acid‐Catalyzed α‐Allylation of Aldehydes with Allylic Alcohols , 2011 .

[11]  M. Navarro,et al.  Electrochemical allylation of aldehydes in a solvent-free cavity cell with a graphite powder cathode , 2011 .

[12]  Ping Liu,et al.  [Cd2(Tren)2(dl-alaninato)] (ClO4)3: An Efficient Water-Compatible Lewis Acid Catalyst for Chemo-, Regio-, and Diastereo-selective Allylation of Various Aldehydes. , 2011 .

[13]  Ping Liu,et al.  [Cd2(tren)2(dl-alaninato)](ClO4)3: an efficient water-compatible Lewis acid catalyst for chemo-, regio-, and diastereo-selective allylation of various aldehydes , 2010 .

[14]  H. Alper,et al.  Rhodium-catalyzed reductive allylation of conjugated aldehydes with allyl acetate. , 2010, The Journal of organic chemistry.

[15]  S. Yin,et al.  Air-stable hypervalent organobismuth(III) tetrafluoroborate as effective and reusable catalyst for the allylation of aldehyde with tetraallyltin , 2010 .

[16]  Jing‐Mei Huang,et al.  Zn-mediated electrochemical allylation of aldehydes in aqueous ammonia. , 2009, Chemical communications.

[17]  K. Szabó,et al.  Performance of SCS palladium pincer complexes in borylation of allylic alcohols. Control of the regioselectivity in the one-pot borylation-allylation process. , 2009, The Journal of organic chemistry.

[18]  Y. Kubota,et al.  Mesoporous aluminosilicate-catalyzed allylation of aldehydes with allylsilanes , 2009 .

[19]  M. Navarro,et al.  Aqueous Barbier allylation of aldehydes mediated by tin. , 2007, Molecules.

[20]  Paul T Anastas,et al.  Innovations and green chemistry. , 2007, Chemical reviews.

[21]  G. Hutchings.  A golden future for green chemistry , 2007 .

[22]  M. Kidwai.  Green chemistry trends toward sustainability , 2007 .

[23]  D. Seyferth.  Alkyl and Aryl Derivatives of the Alkali Metals: Useful Synthetic Reagents as Strong Bases and Potent Nucleophiles. 1. Conversion of Organic Halides to Organoalkali-Metal Compounds , 2006 .

[24]  P. Ramachandran,et al.  Asymmetric allylboration of α, β-enals as a surrogate for the enantioselective synthesis of allylic amines and α-amino acids , 2005 .

[25]  S. Denmark,et al.  Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones , 2003 .

[26]  D. Hall,et al.  Recent advances in the activation of boron and silicon reagents for stereocontrolled allylation reactions. , 2003, Angewandte Chemie.

[27]  R. Batey,et al.  A Mild Protocol for Allylation and Highly Diastereoselective syn or anti Crotylation of Aldehydes in Biphasic and Aqueous Media Utilizing Potassium Allyl‐ and Crotyltrifluoroborates. , 2003 .

[28]  Yoshinori Yamamoto,et al.  SELECTIVE REACTIONS USING ALLYLIC METALS , 1993 .

[29]  Jean-Louis Luche,et al.  Sonochemistry: the use of ultrasonic waves in synthetic organic chemistry , 1989 .

[30]  P. Boudjouk,et al.  Organic sonochemistry. Sonic acceleration of the Reformatsky reaction , 1982 .

[31]  D. D. Perrin,et al.  Purification of Laboratory Chemicals , 2022 .