Page 62 - Book of Invited & Keynotes Talks
P. 62

th
                                   8  Biannual Conference on Chemistry - CHEM 08


                       Multicomponent Synthesis of Novel Heterocycles via Michael
                         Addition, Hantzsch, Biginelli, Baylis-Hillman and π4+ π2
                                               Cycloaddition Reactions

                                             Ismail Abdelshafy Abdelhamid
                       Chemistry Department, Faculty of Science, Cairo University, Giza, Egypt.

                                                        ABSTRACT
                    The reported approaches for the synthesis of heterocycles include carbon-heteroatom
                    bond formation. The synthesis through carbon-carbon bond formation is little bit more
                    difficult, multistep and usually occurs using the transition metals as catalysts for C–H
                    bond functionalization. In our work we managed to achieve this target using the simple
                    reactions that include Michael addition 1–3 , Hantzsch 4–7 , Biginelli 8–10  Baylis-Hillman 11,12
                         4
                             2
                    and π +π  Cycloaddition 13,14  reactions.
                    References :
                    (1)   Ghozlan, S. A. S.; Ramadan, M. A.; Abdelmoniem, A. M.; Abdelhamid, I. A. Arkivoc
                          2019, 30.
                    (2)   Diab, H. M.; Abdelhamid, I. A.; Elwahy, A. H. M. Synlett 2018, 1627.
                    (3)   Abdelhamid, I. A.; Darwish, E. S.; Nasra, M. A.; Abdel-Gallil, F. M.; Fleita, D. H. Synthesis
                          2010, 1107.
                    (4)   Abdelhamid, I. A.; Darweesh, A. F.; Elwahy, A. H. M. Tetrahedron Lett. 2015, 56, 7085.
                    (5)   Abdelmoniem, A. M.; Elwahy, A. H. M.; Abdelhamid, I. A. Arkivoc 2016, iii, 304.
                    (6)   Kassab, R. M.; Elwahy, A. H. M.; Abdelhamid, I. A. Monatshefte für Chemie - Chem.
                          Mon. 2016, 147, 1227.
                    (7)   Mohamed, M. F.; Darweesh, A. F.; Elwahy, A. H. M.; Abdelhamid, I. A. RSC Adv. 2016,
                          6, 40900.
                    (8)   Darwish, E. S.; Abdelhamid, I. A.; Nasra, M. A.; Abdel-Gallil, F. M.; Fleita, D. H. Helv.
                          Chim. Acta 2010, 93, 1204.
                    (9)   Ghozlan, S. A. S.; Abdelhamid, I. A.; Gaber, H.; Elnagdi, M. H. J. Chem. Res. 2004, 2004,
                          789.
                    (10)   M.E. Hassaneen, H.; A. Abdelhamid, I. Curr. Org. Synth. 2013, 10, 974.
                    (11)   Abdelhamid, I. A.; Darwish, E. S.; Nasra, M. A.; Abdel-gallil, F. M.; Fleita, D. H. Arkivoc
                          2008, 2008, 117.
                    (12)   Al-Awadi, N. A.; Ibrahim, M. R.; Abdelhamid, I. A.; Elnagdi, M. H. Tetrahedron 2008, 64,
                          8202.
                    (13)   Abdelhamid, I. A.; Habib, O. M. A.; Butenschön, H. European J. Org. Chem. 2011, 2011,
                          4877.
                    (14)   Al-Mousawi, S. M.; Abdelhamid, I. A.; Moustafa, S. Arkivoc 2007, 2007, 213.












                   BOOK OF INVITED SPEAKERS & KEYNOTES                  CHEM 08 (2020)            Page 62
   57   58   59   60   61   62   63   64   65   66   67