| Year |
Citation |
Score |
| 2022 |
Flores O, Locquet P, Suffert J. An Alternative Route to Complex Allenes or Cyclooctatrienes via a Suzuki Cyclocarbopalladation Cascade. Chemistry (Weinheim An Der Bergstrasse, Germany). 28: e202103502. PMID 34735041 DOI: 10.1002/chem.202103502 |
0.372 |
|
| 2021 |
Flores O, Wagner P, Suffert J. Cyclocarbopalladation/Stille Cascade: Stereoselective Access to Quaternary Functionalized Carbons. Organic Letters. PMID 34375102 DOI: 10.1021/acs.orglett.1c02400 |
0.362 |
|
| 2019 |
Salacz L, Girard N, Suffert J, Blond G. Synthesis of Aromatic Rings Embedded in Polycyclic Scaffolds by Triyne Cycloaddition: Competition between Carbonylative and Non-Carbonylative Pathways. Molecules (Basel, Switzerland). 24. PMID 30736454 DOI: 10.3390/Molecules24030595 |
0.499 |
|
| 2018 |
Salacz L, Girard N, Blond G, Suffert J. Synthesis of Polyheterocyclic Tropones by [2 + 2 + 2 + 1] Carbonylative Cycloaddition of Triynes. Organic Letters. PMID 29943991 DOI: 10.1021/Acs.Orglett.8B01496 |
0.509 |
|
| 2018 |
Salacz L, Girard N, Suffert J, Blond G. Carbonylative cycloaddition for the synthesis of medium-sized carbo- and heterocycles Monatshefte FüR Chemie - Chemical Monthly. 149: 671-686. DOI: 10.1007/S00706-017-2136-0 |
0.399 |
|
| 2018 |
Blouin S, Pertschi R, Schoenfelder A, Suffert J, Blond G. Molecular Diversity of Cyclooctatetraenes through Palladium-Catalyzed Cascade Reactions Advanced Synthesis & Catalysis. 360: 2166-2171. DOI: 10.1002/Adsc.201800110 |
0.483 |
|
| 2017 |
Wagner P, Gulea M, Suffert J, Donnard M. Synthesis of Benzo[c]silole derivatives Bearing a Tetrasubstituted Exocyclic C=C Double Bond by Palladium-Catalyzed Domino Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28422328 DOI: 10.1002/Chem.201701736 |
0.687 |
|
| 2017 |
Salacz L, Charpentier C, Suffert J, Girard N. Desymmetrizing Hydroformylation of Dihydromuconic Acid Diesters: Application to the Synthesis of (+/-)-Vindeburnol. The Journal of Organic Chemistry. PMID 28124911 DOI: 10.1021/Acs.Joc.6B02939 |
0.467 |
|
| 2017 |
Suffert J, Blouin S, Blond G, Donnard M, Gulea M. Cyclocarbopalladation as a Key Step in Cascade Reactions: Recent Developments Synthesis. 49: 1767-1784. DOI: 10.1055/S-0036-1588708 |
0.699 |
|
| 2017 |
Joussot J, Schoenfelder A, Suffert J, Blond G. Synthesis of original polycycles containing five-, six- and seven-membered rings through cyclocarbopalladations/C–H activation cascade reactions Comptes Rendus Chimie. 20: 665-681. DOI: 10.1016/J.Crci.2017.01.005 |
0.465 |
|
| 2017 |
Castanheiro T, Schoenfelder A, Suffert J, Donnard M, Gulea M. Comparative study on the reactivity of propargyl and alkynyl sulfides in palladium-catalyzed domino reactions Comptes Rendus Chimie. 20: 624-633. DOI: 10.1016/J.Crci.2016.12.007 |
0.701 |
|
| 2016 |
Castanheiro T, Suffert J, Gulea M, Donnard M. Aerobic Copper-Mediated Domino Three-Component Approach to 2-Aminobenzothiazole Derivatives. Organic Letters. PMID 27192105 DOI: 10.1021/Acs.Orglett.6B00967 |
0.708 |
|
| 2016 |
Blouin S, Gandon V, Blond G, Suffert J. Synthesis of Cyclooctatetraenes through a Palladium-Catalyzed Cascade Reaction. Angewandte Chemie (International Ed. in English). PMID 27135905 DOI: 10.1002/Anie.201602586 |
0.509 |
|
| 2016 |
Castanheiro T, Suffert J, Donnard M, Gulea M. Synthesis of sulfur heterocycles via domino metal-mediated reactions Phosphorus, Sulfur, and Silicon and the Related Elements. 192: 162-165. DOI: 10.1080/10426507.2016.1255621 |
0.693 |
|
| 2016 |
Suffert J, Blond G, Ghosh N, Maiereanu C. Hopping of Palladium: Access to Original Polycyclic Structures Containing Three-, Four-, Five- and Six-Membered Rings Synlett. 28: 451-455. DOI: 10.1055/S-0036-1588658 |
0.454 |
|
| 2016 |
Joussot J, Schoenfelder A, Larquetoux L, Nicolas M, Suffert J, Blond G. Synthesis of 3-Substituted Chromones and Quinolones from Enaminones Synthesis. 48: 3364-3372. DOI: 10.1055/S-0035-1562513 |
0.478 |
|
| 2015 |
Castanheiro T, Suffert J, Donnard M, Gulea M. Recent advances in the chemistry of organic thiocyanates. Chemical Society Reviews. PMID 26658383 DOI: 10.1039/C5Cs00532A |
0.623 |
|
| 2014 |
Regenass P, Margathe JF, Mann A, Suffert J, Hibert M, Girard N, Bonnet D. Diastereoselective synthesis of novel aza-diketopiperazines via a domino cyclohydrocarbonylation/addition process. Chemical Communications (Cambridge, England). 50: 9657-60. PMID 25019687 DOI: 10.1039/C4Cc03660C |
0.482 |
|
| 2014 |
Castanheiro T, Donnard M, Gulea M, Suffert J. Cyclocarbopalladation/cross-coupling cascade reactions in sulfide series: access to sulfur heterocycles. Organic Letters. 16: 3060-3. PMID 24820009 DOI: 10.1021/Ol501165H |
0.724 |
|
| 2014 |
Castanheiro T, Gulea M, Donnard M, Suffert J. Practical access to aromatic thiocyanates by CuCN-mediated direct aerobic oxidative cyanation of thiophenols and diaryl disulfides European Journal of Organic Chemistry. 2014: 7814-7817. DOI: 10.1002/Ejoc.201403279 |
0.657 |
|
| 2014 |
Boudhar A, Charpenay M, Blond G, Suffert J. Corrigendum: Fenestranes in Synthesis: Unique and Highly Inspiring Scaffolds Angewandte Chemie International Edition. 53: 911-911. DOI: 10.1002/anie.201310665 |
0.3 |
|
| 2013 |
Boudhar A, Charpenay M, Blond G, Suffert J. Fenestranes in synthesis: unique and highly inspiring scaffolds. Angewandte Chemie (International Ed. in English). 52: 12786-98. PMID 24281879 DOI: 10.1002/Anie.201304555 |
0.366 |
|
| 2013 |
Charpenay M, Boudhar A, Hulot C, Blond G, Suffert J. Expeditious cascade reactions: Controlled syntheses of fenestradienes and cyclooctatrienes under palladium catalysis Tetrahedron. 69: 7568-7591. DOI: 10.1016/J.Tet.2013.05.089 |
0.52 |
|
| 2013 |
Boudhar A, Charpenay M, Blond G, Suffert J. Fenestrane in der Synthese: einzigartige und inspirierende Grundgerüste Angewandte Chemie. 125: 13020-13032. DOI: 10.1002/Ange.201304555 |
0.331 |
|
| 2012 |
Charpenay M, Boudhar A, Blond G, Suffert J. An expeditious and atom-economical synthesis of a new generation of substituted [4.6.4.6]fenestradienes. Angewandte Chemie (International Ed. in English). 51: 4379-82. PMID 22438292 DOI: 10.1002/Anie.201107934 |
0.502 |
|
| 2011 |
Petrignet J, Boudhar A, Blond G, Suffert J. Step-economical synthesis of taxol-like tricycles through a palladium-catalyzed domino reaction. Angewandte Chemie (International Ed. in English). 50: 3285-9. PMID 21381167 DOI: 10.1002/Anie.201007751 |
0.531 |
|
| 2011 |
Charpenay M, Boudhar A, Siby A, Schigand S, Blond G, Suffert J. New palladium-catalyzed cascades: 4-exo-dig cyclocarbopalladation reaction followed by suzuki-miyaura or sonogashira cross-coupling Advanced Synthesis and Catalysis. 353: 3151-3156. DOI: 10.1002/Adsc.201100465 |
0.486 |
|
| 2010 |
BRUECKNER R, SCHEUPLEIN SW, SUFFERT J. ChemInform Abstract: Rapid and Stereoselective Synthesis of Dienediynes Related to the Neocarcinostatin Chromophore. Cheminform. 23: no-no. DOI: 10.1002/chin.199202161 |
0.318 |
|
| 2008 |
Blond G, Bour C, Salem B, Suffert J. A new pd-catalyzed cascade reaction for the synthesis of strained aromatic polycycles. Organic Letters. 10: 1075-8. PMID 18275204 DOI: 10.1021/Ol702855H |
0.685 |
|
| 2006 |
Bour C, Blond G, Salem B, Suffert J. 4-exo-dig and 5-exo-dig Cyclocarbopalladations: an expeditious solution toward molecular complexity? Tetrahedron. 62: 10567-10581. DOI: 10.1016/J.Tet.2006.06.116 |
0.684 |
|
| 2006 |
Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-Membered Ring Analogues of the Dienediyne Core of Neocarzinostatine Chromophore by Palladium(0)-Mediated Ring-Closure Reaction Liebigs Annalen. 1996: 447-456. DOI: 10.1002/jlac.199619960405 |
0.565 |
|
| 2006 |
Bour C, Suffert J. 4-exo-dig cyclocarbopalladation: A straightforward synthesis of cyclobutanediols from acyclic γ-bromopropargylic diols under microwave irradiation conditions European Journal of Organic Chemistry. 1390-1395. DOI: 10.1002/Ejoc.200500813 |
0.675 |
|
| 2005 |
Mota AJ, Dedieu A, Bour C, Suffert J. Cyclocarbopalladation involving an unusual 1,5-palladium vinyl to aryl shift as termination step: theoretical study of the mechanism. Journal of the American Chemical Society. 127: 7171-82. PMID 15884959 DOI: 10.1021/Ja050453+ |
0.634 |
|
| 2005 |
Bour C, Suffert J. Cyclocarbopalladation: sequential cyclization and C-h activation/Stille cross-coupling in the Pd-5-exo-dig reaction. Organic Letters. 7: 653-6. PMID 15704917 DOI: 10.1021/Ol047537S |
0.689 |
|
| 2003 |
Salem B, Delort E, Klotz P, Suffert J. Cyclocarbopalladation: 5-exo-dig cyclization versus direct Stille cross-coupling reaction. The influence of the alpha,beta-propargylic substitution. Organic Letters. 5: 2307-10. PMID 12816435 DOI: 10.1021/Ol034647A |
0.504 |
|
| 2003 |
Salem B, Klotz P, Suffert J. Cyclocarbopalladation: formation of bicyclic 1,2-cyclobutanediols through a rare 4-exo-dig cyclization. Organic Letters. 5: 845-8. PMID 12633087 DOI: 10.1021/ol0274965 |
0.365 |
|
| 2002 |
Brückner S, Abraham E, Klotz P, Suffert J. Cascade cyclization: an easy access to highly unsaturated polycyclic ring systems through a tandem stille/[4 + 2] reaction under mild conditions. Organic Letters. 4: 3391-3. PMID 12323026 DOI: 10.1021/ol0264253 |
0.388 |
|
| 2002 |
Abraham E, Suffert J. In situ generation of 1-propyne: A useful introduction of 1-propyne on unsaturated halogenated compounds through the sonogashira reaction Synlett. 328-330. |
0.317 |
|
| 2001 |
Morice C, Domostoj M, Briner K, Mann A, Suffert J, Wermuth CG. Synthesis of constrained arylpiperidines using intramolecular Heck or radical reactions Tetrahedron Letters. 42: 6499-6502. DOI: 10.1016/S0040-4039(01)01191-1 |
0.419 |
|
| 2000 |
Suffert J, Raeppel S, Raeppel F, Didier B. Straightforward access to [6]metacyclophene-based enynes by an inter- intramolecular tandem etherification through a one-pot double S(N)Ar reaction Synlett. 874-876. DOI: 10.1055/S-2000-6703 |
0.418 |
|
| 1999 |
Brückner R, Suffert J. The Bis(enol triflate) Route to Dienediyne Models of the Biradical Forming and DNA-Cleaving Natural Product Neocarzinostatin Chromophore Synlett. 1999: 657-679. DOI: 10.1055/s-1999-2699 |
0.378 |
|
| 1998 |
Raeppel S, Raeppel F, Suffert J. Novel exploration of the SNAr reaction Synlett. 794-796. DOI: 10.1055/S-1998-1762 |
0.443 |
|
| 1998 |
Raeppel S, Toussaint D, Suffert J. Towards a new type of aromatic diynes activation : Synthesis of a novel bicyclic enediyne Synlett. 537-539. DOI: 10.1055/S-1998-1693 |
0.395 |
|
| 1997 |
Raeppel S, Toussaint D, Suffert J. An Alternative Synthesis of Both Enantiomers of trans-3,4-Bis(benzyloxy)cyclopentanone Synlett. 1997: 1061-1062. DOI: 10.1055/S-1997-1524 |
0.446 |
|
| 1996 |
Rohr M, Toussaint D, Chayer S, Mann A, Suffert J, Wermuth CG. Convenient preparation of 3-methoxycarbonylpyridazines by palladium catalyzed alkoxycarbonylation of pyridazinetriflates Heterocycles. 43: 1459-1464. |
0.406 |
|
| 1996 |
Brickmann K, Hambloch F, Suffert J, Brückner R. Synthesis of 6-/10-membered ring analogs of the dienediyne core of the neocarzinostatin chromophore by palladium(0)-mediated ring-closure reactions Liebigs Annales. 457-471. |
0.41 |
|
| 1996 |
Suffert J, Abraham E, Raeppel S, Brückner R. Synthesis of 5-/10-membered ring analogues of the dienediyne core of neocarzinostatine chromophore by palladium(0)-mediated ring-closure reaction Liebigs Annales. 447-456. |
0.411 |
|
| 1995 |
Eckhardt M, Brückner R, Suffert J. The first 6-membered/10-membered ring analogues of the dienediyne core of neocarzinostatin chromophore Tetrahedron Letters. 36: 5167-5170. DOI: 10.1016/0040-4039(95)01025-D |
0.532 |
|
| 1994 |
Solladié-Cavallo A, Csaky AG, Gantz I, Suffert J. Diastereoselective alkylation of 8-phenylmenthyl phenylacetate: Aggregated lithium enolate versus "naked" enolate Journal of Organic Chemistry. 59: 5343-5346. DOI: 10.1021/Jo00097A041 |
0.359 |
|
| 1994 |
Moniatte M, Eckhardt M, Brickmann K, Brückner R, Suffert J. Study of the regioselectivity of palladium-catalyzed monocouplings between conjugated bis(enoltriflates) and trimethylsilylacetylene Tetrahedron Letters. 35: 1965-1968. DOI: 10.1016/S0040-4039(00)73023-1 |
0.664 |
|
| 1994 |
Toussaint D, Suffert J, Wermuth CG. Synthesis of 3-alkynylpyridazines from 3-trifluoromethanesulfonylpyridazines Heterocycles. 38: 1273-1286. |
0.317 |
|
| 1993 |
Suffert J, Eggers A, Scheuplein SW, Brückner R. Contrasteric regioselectivity of palladium(O) catalyzed couplings of alkynes with a bis(enoltriflate). Novel syntheses of E-configurated dienediynes Tetrahedron Letters. 34: 4177-4180. DOI: 10.1016/S0040-4039(00)60521-X |
0.484 |
|
| 1993 |
Scheuplein SW, Machinek R, Suffert J, Brückner R. Activation of a dienediyne model of neocarzinostatin chromophore through an acid mediated solvolysis. Evidence for a new cyclization mode of enyne[3]cumulenes Tetrahedron Letters. 34: 6549-6552. DOI: 10.1016/0040-4039(93)88101-N |
0.508 |
|
| 1992 |
Scheuplein SW, Harms K, Brückner R, Suffert J. Regiocontrol in Pd(0)-Mediated Couplings of a Bis(enol triflate) with Alkynes — Stereoselective Syntheses of Monocyclic Dienediynes Related to the Neocarzinostatin Chromophore Chemische Berichte. 125: 271-278. DOI: 10.1002/cber.19921250143 |
0.462 |
|
| 1991 |
Suffert J, Brückner R. Palladium catalyzed couplings of enol triflates with alkynes under very mild conditions - the stereoselective synthesis of dienediynes from bis(enoltriflates) Tetrahedron Letters. 32: 1453-1456. DOI: 10.1016/0040-4039(91)80356-B |
0.725 |
|
| 1991 |
Brückner R, Scheuplein SW, Suffert J. Rapid and stereoselective construction of dienediynes related to the neocarzinostatin chromophore Tetrahedron Letters. 32: 1449-1452. DOI: 10.1016/0040-4039(91)80355-A |
0.381 |
|
| 1990 |
Suffert J. Synthesis of a new 10-membered ring functionalised cyclodiynol related to neocarziostatin chromophore Tetrahedron Letters. 31: 7437-7440. DOI: 10.1016/S0040-4039(00)88509-3 |
0.304 |
|
| 1988 |
Wender PA, Harmata M, Jeffrey D, Mukai C, Suffert J. Studies on DNA - active agents: The synthesis of the parent carbocyclic subunit of neocarzinostatin chromophore A Tetrahedron Letters. 29: 909-912. DOI: 10.1016/S0040-4039(00)82479-X |
0.593 |
|
| 1980 |
Solladié-Cavallo A, Suffert J, Haesslein J. New Arene(dicarbonyl)chromium Chelates: Application to Asymmetric Synthesis of Amines Angewandte Chemie International Edition in English. 19: 1005-1006. DOI: 10.1002/anie.198010051 |
0.338 |
|
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