| Year |
Citation |
Score |
| 2024 |
Colombo S, Oble J, Poli G, Lo Presti L, Macetti G, Contini A, Broggini G, Papis M, Loro C. Doubly Metathetic NiCl-Catalyzed Coupling Between Bis(2-oxazolines) and Aldehydes: A Novel Access to Bis(ester-imine) Derivatives. Molecules (Basel, Switzerland). 29. PMID 39683917 DOI: 10.3390/molecules29235756 |
0.365 |
|
| 2024 |
Di Matteo M, Gagliardi A, Pradal A, Veiros LF, Gallou F, Poli G. Pd-Catalyzed C(sp)-H/C(sp)-H Coupling of Limonene. The Journal of Organic Chemistry. PMID 39025478 DOI: 10.1021/acs.joc.4c00501 |
0.383 |
|
| 2023 |
Papis M, Bucci R, Contini A, Gelmi ML, Lo Presti L, Poli G, Broggini G, Loro C. Phosphine-Catalyzed Domino Regio- and Stereo-Selective Hexamerization of 2-(Bromomethyl)acrylates to 1,2-Bis(cyclohexenyl)ethenyl Derivatives. Organic Letters. 25: 7380-7384. PMID 37772494 DOI: 10.1021/acs.orglett.3c02836 |
0.366 |
|
| 2023 |
Loro C, Papis M, Foschi F, Broggini G, Poli G, Oble J. Copper(II)-Catalyzed Three-Component Arylation/Hydroamination Cascade from Allyl Alcohol: Access to 1-Aryl-2-sulfonylamino-propanes. The Journal of Organic Chemistry. 88: 13995-14003. PMID 37747795 DOI: 10.1021/acs.joc.3c01536 |
0.396 |
|
| 2022 |
Curpanen S, Reichert P, Lupidi G, Poli G, Oble J, Perez-Luna A. Modular synthesis of 2-furyl carbinols from 3-benzyldimethylsilylfurfural platforms relying on oxygen-assisted C-Si bond functionalization. Beilstein Journal of Organic Chemistry. 18: 1256-1263. PMID 36158173 DOI: 10.3762/bjoc.18.131 |
0.426 |
|
| 2022 |
Sala R, Kiala G, Veiros LF, Broggini G, Poli G, Oble J. Redox-Neutral Ru(0)-Catalyzed Alkenylation of 2-Carboxaldimine-heterocyclopentadienes. The Journal of Organic Chemistry. 87: 4640-4648. PMID 35290058 DOI: 10.1021/acs.joc.1c03044 |
0.325 |
|
| 2020 |
Foschi F, Loro C, Sala R, Oble J, Lo Presti L, Beccalli EM, Poli G, Broggini G. Intramolecular Aminoazidation of Unactivated Terminal Alkenes by Palladium-Catalyzed Reactions with Hydrogen Peroxide as the Oxidant. Organic Letters. 22: 1402-1406. PMID 32027136 DOI: 10.1021/acs.orglett.0c00010 |
0.347 |
|
| 2019 |
Ravasco JMJM, Monteiro CM, Siopa F, Trindade AF, Oble J, Poli G, Simeonov SP, Afonso CAM. Creating Diversity from Biomass: A Tandem Bio/Metal-Catalysis towards Chemoselective Synthesis of Densely Substituted Furans. Chemsuschem. PMID 31531965 DOI: 10.1002/cssc.201902051 |
0.362 |
|
| 2018 |
Liu Y, Mao Z, Pradal A, Huang PQ, Oble J, Poli G. Palladium-Catalyzed [3 + 2]-C-C/N-C Bond-Forming Annulation. Organic Letters. PMID 29897775 DOI: 10.1021/Acs.Orglett.8B01616 |
0.378 |
|
| 2018 |
Roudesly F, Veiros LF, Oble J, Poli G. Pd-Catalyzed Direct C-H Alkenylation and Allylation of Azine N-Oxides. Organic Letters. 20: 2346-2350. PMID 29629776 DOI: 10.1021/acs.orglett.8b00689 |
0.406 |
|
| 2017 |
Pezzetta C, Veiros LF, Oble J, Poli G. Murai Reaction on Furfural Derivatives Enabled by Removable N,N'-Bidentate Directing Groups. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 8385-8389. PMID 28445630 DOI: 10.1002/chem.201701850 |
0.34 |
|
| 2017 |
Bouhalleb G, Mhasni O, Poli G, Rezgui F. Direct palladium-catalyzed allylic alkylations of alcohols with enamines: Synthesis of homoallyl ketones Tetrahedron Letters. 58: 2525-2529. DOI: 10.1016/J.TETLET.2017.05.024 |
0.329 |
|
| 2017 |
Borelli T, Brenna S, Broggini G, Oble J, Poli G. (Diacyloxyiodo)benzenes-Driven Palladium-Catalyzed Cyclizations of UnsaturatedN-Sulfonylamides: Opportunities of Path Selection Advanced Synthesis & Catalysis. 359: 623-628. DOI: 10.1002/ADSC.201600813 |
0.356 |
|
| 2016 |
Ramirez Hernandez J, Chemla F, Ferreira F, Jackowski O, Oble J, Perez-Luna A, Poli G. tert-Butanesulfinamides as Nitrogen Nucleophiles in Carbon-Nitrogen Bond Forming Reactions. Chimia. 70: 84-92. PMID 26931222 DOI: 10.2533/Chimia.2016.84 |
0.461 |
|
| 2016 |
Lorion MM, Duarte FJ, Calhorda MJ, Oble J, Poli G. Opening the Way to Catalytic Aminopalladation/Proxicyclic Dehydropalladation: Access to Methylidene γ-Lactams. Organic Letters. 18: 1020-3. PMID 26902777 DOI: 10.1021/Acs.Orglett.6B00143 |
0.749 |
|
| 2016 |
Lorion MM, Oble J, Poli G. Palladium catalyzed oxidative aminations and oxylations: where are we? Pure and Applied Chemistry. 88: 381-389. DOI: 10.1515/Pac-2015-1102 |
0.804 |
|
| 2016 |
Diamante D, Gabrieli S, Benincori T, Broggini G, Oble J, Poli G. Dehydrogenative Allylic Aminations of But-3-enoic Acid Derivatives Synthesis. 48: 3400-3412. DOI: 10.1055/S-0035-1562453 |
0.356 |
|
| 2016 |
Duarte FJS, Poli G, Calhorda MJ. Mechanistic Study of the Direct Intramolecular Allylic Amination Reaction Catalyzed by Palladium(II) Acs Catalysis. 6: 1772-1784. DOI: 10.1021/Acscatal.5B02091 |
0.445 |
|
| 2016 |
Lorion MM, Oble J, Poli G. ChemInform Abstract: Palladium Catalyzed Oxidative Aminations and Oxylations: Where Are We? Cheminform. 47. DOI: 10.1002/CHIN.201641255 |
0.74 |
|
| 2015 |
Oble J, Poli G, Louafi F, Lorion M. Dichotomous Reaction Pathways for the Oxidative Palladium(II)-Catalyzed Intramolecular Acyloxylation of Alkenes Synlett. 26: 2237-2242. DOI: 10.1055/S-0035-1560071 |
0.779 |
|
| 2015 |
Broggini G, Poli G, Beccalli EM, Brusa F, Gazzola S, Oble J. Ruthenium‐Catalyzed Hydroamination of Aminoallenes: an Approach to Vinyl Substituted Heterocycles Advanced Synthesis & Catalysis. 357: 677-682. DOI: 10.1002/Adsc.201400776 |
0.486 |
|
| 2014 |
Kammerer C, Prestat G, Madec D, Poli G. Synthesis of γ-lactams and γ-lactones via intramolecular Pd-catalyzed allylic alkylations. Accounts of Chemical Research. 47: 3439-47. PMID 25415844 DOI: 10.1021/Ar500178N |
0.545 |
|
| 2014 |
Rajabi J, Lorion MM, Ly VL, Liron F, Oble J, Prestat G, Poli G. Dormant versus evolving aminopalladated intermediates: toward a unified mechanistic scenario in Pd(II)-catalyzed aminations. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1539-46. PMID 24403244 DOI: 10.1002/Chem.201302744 |
0.791 |
|
| 2014 |
Erray I, Rezgui F, Oble J, Poli G. Microwave-Assisted Palladium-Catalyzed Allylation of β-Enaminones Synlett. 25: 2196-2200. DOI: 10.1055/S-0034-1378540 |
0.494 |
|
| 2014 |
Mistico L, Ay E, Huynh V, Bourderioux A, Chemla F, Ferreira F, Oble J, Perez-Luna A, Poli G, Prestat G. Reactivity of tert-butanesulfinamides in palladium-catalyzed allylic substitutions Journal of Organometallic Chemistry. 760: 124-129. DOI: 10.1016/J.Jorganchem.2013.11.026 |
0.575 |
|
| 2014 |
Rigamonti M, Prestat G, Broggini G, Poli G. Synthesis of 1,4-benzodiazepinones via palladium-catalysed allene carbopalladation/amination domino sequence Journal of Organometallic Chemistry. 760: 149-155. DOI: 10.1016/J.Jorganchem.2013.11.010 |
0.568 |
|
| 2014 |
Liron F, Oble J, Lorion MM, Poli G. Direct Allylic Functionalization Through Pd-Catalyzed C-H Activation European Journal of Organic Chemistry. 2014: 5863-5883. DOI: 10.1002/Ejoc.201402049 |
0.779 |
|
| 2014 |
Liron F, Oble J, Lorion MM, Poli G. ChemInform Abstract: Direct Allylic Functionalization Through Pd-Catalyzed C-H Activation Cheminform. 45: no-no. DOI: 10.1002/CHIN.201451242 |
0.737 |
|
| 2014 |
Rigamonti M, Prestat G, Broggini G, Poli G. ChemInform Abstract: Synthesis of 1,4-Benzodiazepinones via Palladium-Catalyzed Allene Carbopalladation/Amination Domino Sequence. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201441195 |
0.364 |
|
| 2014 |
Mistico L, Ay E, Huynh V, Bourderioux A, Chemla F, Ferreira F, Oble J, Perez-Luna A, Poli G, Prestat G. ChemInform Abstract: Reactivity of tert-Butanesulfinamides in Palladium-Catalyzed Allylic Substitutions. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201440060 |
0.479 |
|
| 2014 |
Rajabi J, Lorion MM, Ly VL, Liron F, Oble J, Prestat G, Poli G. Dormant versus evolving aminopalladated intermediates: Toward a unified mechanistic scenario in PdII-catalyzed aminations Chemistry - a European Journal. 20: 1539-1546. DOI: 10.1002/chem.201302744 |
0.783 |
|
| 2013 |
Lorion MM, Matt B, Alves S, Proust A, Poli G, Oble J, Izzet G. Versatile post-functionalization of polyoxometalate platforms by using an unprecedented range of palladium-catalyzed coupling reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 12607-12. PMID 23983072 DOI: 10.1002/Chem.201301694 |
0.763 |
|
| 2013 |
Lorion MM, Gasperini D, Oble J, Poli G. Palladium-catalyzed arylic/allylic aminations: permutable domino sequences for the synthesis of dihydroquinolines from Morita-Baylis-Hillman adducts. Organic Letters. 15: 3050-3. PMID 23734985 DOI: 10.1021/Ol401234V |
0.788 |
|
| 2013 |
Erray I, Oble J, Poli G, Rezgui F. RegioselectiveS-allylation of thiols with cyclic Baylis–Hillman acetates Journal of Sulfur Chemistry. 35: 128-136. DOI: 10.1080/17415993.2013.809453 |
0.429 |
|
| 2013 |
Kammerer-Pentier C, Diez Martinez A, Oble J, Prestat G, Merino P, Poli G. ChemInform Abstract: Dual Reactivity of O-α-Allenyl Esters under Palladium(0) Catalysis: From Carbopalladation/Allylic Alkylation Domino Sequence to Decarboxylative Allenylation. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201304024 |
0.316 |
|
| 2012 |
Giboulot S, Liron F, Prestat G, Wahl B, Sauthier M, Castanet Y, Mortreux A, Poli G. Pd-catalyzed domino carbonylative-decarboxylative allylation: an easy and selective monoallylation of ketones. Chemical Communications (Cambridge, England). 48: 5889-91. PMID 22555554 DOI: 10.1039/C2Cc32391E |
0.526 |
|
| 2012 |
Boutier A, Kammerer-Pentier C, Krause N, Prestat G, Poli G. Pd-catalyzed asymmetric synthesis of N-allenyl amides and their Au-catalyzed cycloisomerizative hydroalkylation: a new route toward enantioenriched pyrrolidones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 3840-4. PMID 22378545 DOI: 10.1002/Chem.201103902 |
0.499 |
|
| 2012 |
Kammerer-Pentier C, Martinez AD, Oble J, Prestat G, Merino P, Poli G. Dual reactivity of O-α-allenyl esters under palladium(0) catalysis: From carbopalladation/allylic alkylation domino sequence to decarboxylative allenylation Journal of Organometallic Chemistry. 714: 53-59. DOI: 10.1016/J.Jorganchem.2012.03.014 |
0.499 |
|
| 2012 |
Broggini G, Borsini E, Fasana A, Poli G, Liron F. Transition-Metal-Catalyzed Hydroamination and Carboamination Reactions of Anthranilic Allenamides as a Route to 2-Vinyl- and 2-(α-Styryl)quinazolin-4-one Derivatives European Journal of Organic Chemistry. 2012: 3617-3624. DOI: 10.1002/Ejoc.201200353 |
0.499 |
|
| 2012 |
Broggini G, Borsini E, Fasana A, Poli G, Liron F. ChemInform Abstract: Transition-Metal-Catalyzed Hydroamination and Carboamination Reactions of Anthranilic Allenamides as a Route to 2-Vinyl- and 2-(α-Styryl)quinazolin-4-one Derivatives. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201248169 |
0.314 |
|
| 2012 |
Wahl B, Giboulot S, Mortreux A, Castanet Y, Sauthier M, Liron F, Poli G. ChemInform Abstract: Straightforward Synthesis of Allylated Keto Esters: The Palladium-Catalyzed Haloketone Alkoxycarbonylation/Allylation Domino Reaction. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201236042 |
0.488 |
|
| 2012 |
Le Duc G, Bernoud E, Prestat G, Cacchi S, Fabrizi G, Iazzetti A, Madec D, Poli G. ChemInform Abstract: Palladium-Catalyzed Aromatic Sulfonylation: A New Catalytic Domino Process Exploiting in situ Generated Sulfinate Anions. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201215073 |
0.358 |
|
| 2012 |
Wahl B, Bonin H, Mortreux A, Giboulot S, Liron F, Poli G, Sauthier M. A General and Efficient Method for the Alkoxycarbonylation of α-Chloro Ketones Advanced Synthesis & Catalysis. 354: 3105-3114. DOI: 10.1002/Adsc.201200378 |
0.426 |
|
| 2012 |
Wahl B, Giboulot S, Mortreux A, Castanet Y, Sauthier M, Liron F, Poli G. Straightforward Synthesis of Allylated Keto Esters: The Palladium-Catalysed Haloketone Alkoxycarbonylation/ Allylation Domino Reaction Advanced Synthesis & Catalysis. 354: 1077-1083. DOI: 10.1002/Adsc.201100848 |
0.566 |
|
| 2011 |
Kleimark J, Prestat G, Poli G, Norrby PO. Palladium-catalyzed allylic sulfinylation and the Mislow-Braverman-Evans rearrangement. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13963-5. PMID 22095834 DOI: 10.1002/Chem.201102937 |
0.58 |
|
| 2011 |
Cacchi S, Fabrizi G, Goggiamani A, Iazzetti A, Madec D, Poli G, Prestat G. Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters. Organic & Biomolecular Chemistry. 9: 8233-6. PMID 22041862 DOI: 10.1039/C1Ob06593A |
0.508 |
|
| 2011 |
Zaborova E, Deschamp J, Guieu S, Blériot Y, Poli G, Ménand M, Madec D, Prestat G, Sollogoub M. Cavitand supported tetraphosphine: cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling. Chemical Communications (Cambridge, England). 47: 9206-8. PMID 21743893 DOI: 10.1039/C1Cc12241J |
0.392 |
|
| 2011 |
Bantreil X, Prestat G, Moreno A, Madec D, Fristrup P, Norrby PO, Pregosin PS, Poli G. γ- and δ-lactams through palladium-catalyzed intramolecular allylic alkylation: enantioselective synthesis, NMR Investigation, and DFT rationalization. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 2885-96. PMID 21294194 DOI: 10.1002/Chem.201001300 |
0.559 |
|
| 2011 |
Madec D, Poli G, Le Duc G, Bernoud E, Prestat G, Cacchi S, Fabrizi G, Iazzetti A. Palladium-Catalyzed Aromatic Sulfonylation: A New Catalytic Domino Process Exploiting in situ Generated Sulfinate Anions Synlett. 2011: 2943-2946. DOI: 10.1055/S-0031-1289880 |
0.455 |
|
| 2010 |
Bernoud E, Le Duc G, Bantreil X, Prestat G, Madec D, Poli G. Aryl sulfoxides from allyl sulfoxides via [2,3]-sigmatropic rearrangement and domino Pd-catalyzed generation/arylation of sulfenate anions. Organic Letters. 12: 320-3. PMID 20000488 DOI: 10.1021/Ol902620T |
0.514 |
|
| 2010 |
Bernoud E, Duc GL, Bantreil X, Prestat G, Madec D, Poli G. Domino Palladium-Catalyzed Generation and Arylation of SulfenateAnions Synfacts. 2010: 465-465. DOI: 10.1055/S-0029-1219594 |
0.525 |
|
| 2010 |
Vogel S, Bantreil X, Maitro G, Prestat G, Madec D, Poli G. Palladium-catalyzed intramolecular allylic alkylation of α-sulfinyl carbanions: a new asymmetric route to enantiopure γ-lactams Tetrahedron Letters. 51: 1459-1461. DOI: 10.1016/J.Tetlet.2010.01.012 |
0.529 |
|
| 2010 |
Maitro G, Prestat G, Madec D, Poli G. An escapade in the world of sulfenate anions: generation, reactivity and applications in domino processes Tetrahedron: Asymmetry. 21: 1075-1084. DOI: 10.1016/J.Tetasy.2010.05.035 |
0.415 |
|
| 2010 |
Poli G, Giambastiani G. ChemInform Abstract: Regio- and Stereocontrol in Rhodium-Catalyzed Allylic Substitutions Cheminform. 33: no-no. DOI: 10.1002/CHIN.200201281 |
0.45 |
|
| 2010 |
Poli G, Giambastiani G. ChemInform Abstract: Palladium-Catalyzed Domino Processes Cheminform. 32: no-no. DOI: 10.1002/CHIN.200152261 |
0.314 |
|
| 2010 |
Poli G, Giambastiani G, Malacria M, Thorimbert S. ChemInform Abstract: Silylated Pyrrolidones via Diastereoselective Pd-Catalyzed Intramolecular Allylic Alkylations. Cheminform. 32: no-no. DOI: 10.1002/chin.200146111 |
0.393 |
|
| 2010 |
Poli G, Giambastiani G, Pacini B. ChemInform Abstract: Pd(0)-Catalyzed Allylic Alkylation/Heck Coupling in Domino Sequence. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200146107 |
0.364 |
|
| 2010 |
Giambastiani G, Poli G. ChemInform Abstract: Palladium-Catalyzed Alkylation with Allylic Acetates under Neutral Conditions. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199922061 |
0.417 |
|
| 2010 |
REGINATO G, MORDINI A, MESSINA F, DEGL'INNOCENTI A, POLI G. ChemInform Abstract: A New Stereoselective Synthesis of Chiral γ-Functionalized (E)- Allylic Amines. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199650198 |
0.301 |
|
| 2010 |
BELVISI L, GENNARI C, POLI G, SCOLASTICO C, SALOM B. ChemInform Abstract: Stereoselective Radical-Mediated Cyclization of Norephedrine Derived o- Bromobenzamides: Enantioselective Synthesis of 4-Substituted 1,2,3,4- Tetrahydroisoquinolines. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199325067 |
0.317 |
|
| 2010 |
BERNARDI A, DOTTI P, POLI G, SCOLASTICO C. ChemInform Abstract: Stereoselective Michael Additions of Titanium “Ate” Complexes of Ketone and Ester Enolates. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199243071 |
0.324 |
|
| 2010 |
PASQUARELLO A, POLI G, SCOLASTICO C. ChemInform Abstract: Stereoselective Reduction of 2-Methylacetoacetaldehydes Protected as Norephedrine-Derived Oxazolidines: A New Access to Enantiomerically Pure “Propanal-Type” Aldols. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199233070 |
0.302 |
|
| 2009 |
Nahra F, Liron F, Prestat G, Mealli C, Messaoudi A, Poli G. Striking AcOH acceleration in direct intramolecular allylic amination reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11078-82. PMID 19795438 DOI: 10.1002/Chem.200901946 |
0.463 |
|
| 2009 |
Liron F, Fontana F, Zirimwabagabo JO, Prestat G, Rajabi J, La Rosa C, Poli G. A new cross-coupling-based synthesis of carpanone. Organic Letters. 11: 4378-81. PMID 19725522 DOI: 10.1021/Ol9017326 |
0.515 |
|
| 2009 |
Kammerer C, Prestat G, Madec D, Poli G. Phosphine-free palladium-catalyzed allene carbopalladation/allylic alkylation domino sequence: a new route to 4-(alpha-styryl) gamma-lactams. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 4224-7. PMID 19301328 DOI: 10.1002/Chem.200900184 |
0.449 |
|
| 2009 |
Bantreil X, Prestat G, Madec D, Fristrup P, Poli G. Enantioselective γ-lactam synthesis via palladium-catalyzed intramolecular asymmetric allylic alkylation Synlett. 1441-1444. DOI: 10.1055/S-0029-1216747 |
0.525 |
|
| 2009 |
Kammerer C, Prestat G, Madec D, Poli G. ChemInform Abstract: Phosphine-Free Palladium-Catalyzed Allene Carbopalladation/Allylic Alkylation Domino Sequence: A New Route to 4-(α-Styryl) γ-Lactams. Cheminform. 40. DOI: 10.1002/CHIN.200935114 |
0.372 |
|
| 2009 |
Nahra F, Liron F, Prestat G, Mealli C, Messaoudi A, Poli G. Inside Cover: Striking AcOH Acceleration in Direct Intramolecular Allylic Amination Reactions (Chem. Eur. J. 42/2009) Chemistry - a European Journal. 15: 11038-11038. DOI: 10.1002/Chem.200990164 |
0.475 |
|
| 2008 |
Vitale M, Prestat G, Lopes D, Madec D, Kammerer C, Poli G, Girnita L. New picropodophyllin analogs via palladium-catalyzed allylic alkylation-Hiyama cross-coupling sequences. The Journal of Organic Chemistry. 73: 5795-805. PMID 18576606 DOI: 10.1021/Jo800707Q |
0.784 |
|
| 2008 |
Kammerer C, Prestat G, Gaillard T, Madec D, Poli G. Allylic alkylation and ring-closing metathesis in sequence: a successful cohabitation of Pd and Ru. Organic Letters. 10: 405-8. PMID 18183995 DOI: 10.1021/Ol702694V |
0.513 |
|
| 2008 |
Madec D, Poli G, Mingoia F, Prestat G. N-Substituted Tetronamides as Ambident Nucleophilic Building Blocks for the Synthesis of New 4-Aza-2,3-didehydropodophyllotoxins Synlett. 2008: 1475-1478. DOI: 10.1055/S-2008-1078429 |
0.424 |
|
| 2008 |
Mingoia F, Vitale M, Madec D, Prestat G, Poli G. Pseudo-domino palladium-catalyzed allylic alkylation/Mizoroki–Heck coupling reaction: a key sequence toward (±)-podophyllotoxin Tetrahedron Letters. 49: 760-763. DOI: 10.1016/J.Tetlet.2007.11.202 |
0.771 |
|
| 2007 |
Maitro G, Vogel S, Sadaoui M, Prestat G, Madec D, Poli G. Enantioselective synthesis of aryl sulfoxides via palladium-catalyzed arylation of sulfenate anions. Organic Letters. 9: 5493-6. PMID 18034497 DOI: 10.1021/Ol702343G |
0.456 |
|
| 2007 |
Madec D, Poli G, Thuong M, Sottocornola S, Prestat G, Broggini G. New Access to Kainic Acid via Intramolecular Palladium-Catalyzed Allylic Alkylation Synlett. 2007: 1521-1524. DOI: 10.1055/S-2007-982542 |
0.533 |
|
| 2007 |
Merino P, Tejero T, Mannucci V, Prestat G, Madec D, Poli G. Hydroxylamine Oxygen as Nucleophile in Palladium(0)- and Palladium(II)-Catalyzed Allylic Alkylation: A Novel Access to Isoxazolidines. Cheminform. 38. DOI: 10.1055/S-2007-973868 |
0.569 |
|
| 2007 |
Merino P, Poli G, Tejero T, Mannucci V, Prestat G, Madec D. Hydroxylamine Oxygen as Nucleophile in Palladium(0)- and Palladium(II)-Catalyzed Allylic Alkylation: A Novel Access to Isoxazolidines Synlett. 2007: 0944-0948. DOI: 10.1055/S-2007-973868 |
0.365 |
|
| 2007 |
Vitale M, Prestat G, Lopes D, Madec D, Poli G. A Palladium-Catalyzed Sequence of Allylic Alkylation and Hiyama Cross-Coupling: Convenient Synthesis of 4-(α-Styryl) γ-Lactones. Cheminform. 38. DOI: 10.1002/CHIN.200701105 |
0.365 |
|
| 2006 |
Maitro G, Vogel S, Prestat G, Madec D, Poli G. Aryl sulfoxides via palladium-catalyzed arylation of sulfenate anions. Organic Letters. 8: 5951-4. PMID 17165902 DOI: 10.1021/Ol062315A |
0.527 |
|
| 2006 |
Maitro G, Prestat G, Madec D, Poli G. Preparation of allyl sulfoxides by palladium-catalyzed allylic alkylation of sulfenate anions. The Journal of Organic Chemistry. 71: 7449-54. PMID 16958541 DOI: 10.1021/Jo061359U |
0.549 |
|
| 2006 |
Poli G, Vitale M, Prestat G, Lopes D, Madec D. A Palladium-Catalyzed Sequence of Allylic Alkylation and Hiyama Cross-Coupling: Convenient Synthesis of 4-(α-Styryl) γ-Lactones Synlett. 2006: 2231-2234. DOI: 10.1055/S-2006-949651 |
0.791 |
|
| 2006 |
Ferber B, Prestat G, Vogel S, Madec D, Poli G. Synthesis of 3,5-Disubstituted Piperazinones via Palladium(II)-Catalyzed Amination. Cheminform. 37. DOI: 10.1055/S-2006-948208 |
0.559 |
|
| 2006 |
Prestat G, Poli G, Ferber B, Vogel S, Madec D. Synthesis of 3,5-Disubstituted Piperazinones via Palladium(II)-Catalyzed Amination Synlett. 2006: 2133-2135. DOI: 10.1055/S-2006-948208 |
0.353 |
|
| 2006 |
Madec D, Poli G, Maitro G, Prestat G. Palladium-Catalyzed Allylic Alkylation of α-Sulfinyl Carbanions under Biphasic Conditions Synlett. 2006: 1055-1058. DOI: 10.1055/S-2006-939702 |
0.518 |
|
| 2006 |
Maitro G, Prestat G, Madec D, Poli G. Palladium-Catalyzed Allylic Alkylation of α-Sulfinyl Carbanions under Biphasic Conditions. Cheminform. 37. DOI: 10.1002/CHIN.200635077 |
0.37 |
|
| 2005 |
Madec D, Prestat G, Martini E, Fristrup P, Poli G, Norrby PO. Surprisingly mild "enolate-counterion-free"pd(0)-catalyzed intramolecular allylic alkylations. Organic Letters. 7: 995-8. PMID 15760122 DOI: 10.1002/CHIN.200532121 |
0.562 |
|
| 2005 |
Madec D, Mingoia F, Macovei C, Maitro G, Giambastiani G, Poli G. New Enantiopure Bis(thioether) and Bis(sulfoxide) Ligands from Benzothiophene European Journal of Organic Chemistry. 2005: 552-557. DOI: 10.1002/Ejoc.200400547 |
0.369 |
|
| 2004 |
Lemaire S, Giambastiani G, Prestat G, Poli G. Pyrrolizidine Alkaloids by Intramolecular Palladium-Catalysed Allylic Alkylation: Synthesis of (±)-Isoretronecanol European Journal of Organic Chemistry. 2004: 2840-2847. DOI: 10.1002/Ejoc.200400135 |
0.432 |
|
| 2004 |
Lemaire S, Giambastiani G, Prestat G, Poli G. Pyrrolizidine Alkaloids by Intramolecular Palladium-Catalyzed Allylic Alkylation: Synthesis of (.+-.)-Isoretronecanol. Cheminform. 35. DOI: 10.1002/CHIN.200446194 |
0.459 |
|
| 2003 |
Bisaro F, Prestat G, Vitale M, Poli G. Alkylation of Active Methylenes via Benzhydryl Cations. Cheminform. 34. DOI: 10.1055/S-2002-34884 |
0.723 |
|
| 2003 |
Norrby PO, Mader MM, Vitale M, Prestat G, Poli G. Rationalizing ring-size selectivity in intramolecular Pd-catalyzed allylations of resonance-stabilized carbanions Organometallics. 22: 1849-1855. DOI: 10.1021/Om030066D |
0.757 |
|
| 2003 |
Ferber B, Lemaire S, Mader MM, Prestat G, Poli G. A new access to 3,5-disubstituted piperazinones via Pd(0)-catalyzed amination Tetrahedron Letters. 44: 4213-4216. DOI: 10.1016/S0040-4039(03)00885-2 |
0.447 |
|
| 2003 |
Lemaire S, Prestat G, Giambastiani G, Madec D, Pacini B, Poli G. Palladium-catalyzed pseudo-domino cyclizations Journal of Organometallic Chemistry. 687: 291-300. DOI: 10.1016/S0022-328X(03)00621-1 |
0.521 |
|
| 2003 |
Thorimbert S, Giambastiani G, Commandeur C, Vitale M, Poli G, Malacria M. Diastereoselective Preparation of Silylated Pyrrolidones through Palladium-Catalysed Cyclisations European Journal of Organic Chemistry. 2003: 2702-2708. DOI: 10.1002/Ejoc.200300086 |
0.731 |
|
| 2003 |
Thorimbert S, Giambastiani G, Commandeur C, Vitale M, Poli G, Malacria M. Diastereoselective Preparation of Silylated Pyrrolidones Through Palladium-Catalyzed Cyclizations. Cheminform. 34. DOI: 10.1002/chin.200344098 |
0.469 |
|
| 2003 |
Ferber B, Lemaire S, Mader MM, Prestat G, Poli G. A New Access to 3,5-Disubstituted Piperazinones via Pd(0)-Catalyzed Amination. Cheminform. 34. DOI: 10.1002/CHIN.200336128 |
0.333 |
|
| 2002 |
Poli G, Giambastiani G. An epiisopicropodophyllin aza analogue via palladium-catalyzed pseudo-domino cyclization. The Journal of Organic Chemistry. 67: 9456-9. PMID 12492354 DOI: 10.1021/Jo026068+ |
0.46 |
|
| 2001 |
Poli G, Giambastiani G, Malacria M, Thorimbert S. Silylated pyrrolidones via diastereoselective Pd-catalysed intramolecular allylic alkylations Tetrahedron Letters. 42: 6287-6289. DOI: 10.1016/S0040-4039(01)01249-7 |
0.484 |
|
| 2001 |
Poli G, Giambastiani G, Pacini B. Pd(0)-catalyzed allylic alkylation/Heck coupling in domino sequence Tetrahedron Letters. 42: 5179-5182. DOI: 10.1016/S0040-4039(01)00951-0 |
0.464 |
|
| 2000 |
Poli G, Giambastiani G, Heumann A. Palladium in Organic Synthesis: Fundamental Transformations and Domino Processes Tetrahedron. 56: 5959-5989. DOI: 10.1016/S0040-4020(00)00438-5 |
0.312 |
|
| 1999 |
Poli G, Giambastiani G, Mordini A. Palladium-Catalyzed Allylic Alkylations via Titanated Nucleophiles: A New Early-Late Heterobimetallic System. The Journal of Organic Chemistry. 64: 2962-2965. PMID 11674378 DOI: 10.1021/Jo982266I |
0.483 |
|
| 1998 |
Giambastiani G, Pacini B, Porcelloni M, Poli G. A New Palladium-Catalyzed Intramolecular Allylation to Pyrrolidin-2-ones(1). The Journal of Organic Chemistry. 63: 804-807. PMID 11672076 DOI: 10.1021/Jo971849+ |
0.528 |
|
| 1998 |
Giambastiani G, Poli G. Palladium Catalyzed Alkylation with Allylic Acetates under Neutral Conditions The Journal of Organic Chemistry. 63: 9608-9609. DOI: 10.1021/Jo981599C |
0.506 |
|
| 1998 |
Bigi A, Mordini A, Thurner A, Faigl F, Poli G, Tõke L. Kinetic resolution of racemic alkoxy oxiranes by chiral lithium amides Tetrahedron: Asymmetry. 9: 2293-2299. DOI: 10.1016/S0957-4166(98)00239-0 |
0.373 |
|
| 1998 |
Reginato G, Mordini A, Degl'Innocenti A, Manganiello S, Capperucci A, Poli G. Stannylcupration of chiral γ-amino acetylenic esters: Stereocontrolled synthesis of 3-tributylstannyl γ-amino (E)-alkenoates a as precursors of 4-stannylated pyrrolinones Tetrahedron. 54: 10227-10238. DOI: 10.1016/S0040-4020(98)00624-3 |
0.482 |
|
| 1998 |
Poli G, Ciofi Baffoni S, Giambastiani G, Reginato G. A new asymmetric approach toward 5-substituted pyrrolidin-2-one derivatives Tetrahedron. 54: 10403-10418. DOI: 10.1016/S0040-4020(98)00494-3 |
0.429 |
|
| 1997 |
Poli G, Maccagni E, Manzoni L, Pilati T, Scolastico C. Diastereoselective addition of metal-coordinated and “naked” nucleophilic reagents to norephedrine derived 2-acyl-N-tosyl-oxazolidines Tetrahedron. 53: 1759-1776. DOI: 10.1016/S0040-4020(96)01087-3 |
0.369 |
|
| 1996 |
Reginato G, Mordini A, Messina F, Degl'Innocenti A, Poli G. A new stereoselective synthesis of chiral γ-functionalized (E)-allylic amines Tetrahedron. 52: 10985-10996. DOI: 10.1016/0040-4020(96)00617-5 |
0.446 |
|
| 1995 |
Poli G, Maccagni E, Manzoni L, Pilati T, Scolastico C. Diastereoselective Addition of Organometallic Reagents to Nor-Ephedrine-Derived 2-Acyl-N-Tosyl-Oxazolidines Synlett. 1995: 71-73. DOI: 10.1055/S-1995-4854 |
0.383 |
|
| 1995 |
Poli G, Ciofi S, Maccagni M, Sardone N. A new asymmetric approach towards 2-pyrrolidinones and pyrrolidines: Simple versus double stereodifferentiation Tetrahedron Letters. 36: 8669-8672. DOI: 10.1016/0040-4039(95)01788-J |
0.376 |
|
| 1993 |
Manzoni L, Poli G, Scolastico C. Asymmetric Synthesis of Enantiopure α-Sulfenyl Dithioacetals and α-Sulfenyl Aldehydes Phosphorus, Sulfur, and Silicon and the Related Elements. 74: 381-382. DOI: 10.1080/10426509308038125 |
0.374 |
|
| 1993 |
Belvisi L, Gennari C, Poli G, Scolastico C, Salom B. Stereoselective radical-mediated cyclization of norephedrine derived o-bromobenzamides: Enantioselective synthesis of 4-substituted 1,2,3,4-tetrahydroisoquinolines Tetrahedron: Asymmetry. 4: 273-280. DOI: 10.1016/S0957-4166(00)82347-2 |
0.39 |
|
| 1992 |
Pasquarello A, Poli G, Scolastico C. Stereoselective Reduction of 2-Methylacetoacetaldehydes Protected as Norephedrine-Derived Oxazolidines: A New Access to Enantiomerically Pure "Propanal-Type" Aldols Synlett. 1992: 93-95. DOI: 10.1055/S-1992-21992 |
0.393 |
|
| 1992 |
Manzoni L, Pilati T, Poli G, Scolastico C. Diastereoselective addition of metal-coordinated and ‘naked’ tri-sec-butylborohydrides to a norephedrine-derived 2-acetyloxazolidine Journal of the Chemical Society, Chemical Communications. 1027-1029. DOI: 10.1039/C39920001027 |
0.312 |
|
| 1992 |
Bernardi A, Cardani S, Poli G, Potenza D, Scolastico C. Norephedrine derived oxazolidines as chiral acylating agents: An NMR study of the intermediate cations. Tetrahedron. 48: 1343-1352. DOI: 10.1016/S0040-4020(01)90796-3 |
0.451 |
|
| 1992 |
Belvisi L, Gennari C, Poli G, Scolastico C, Salom B, Vassallo M. Stereoselective radical-mediated cyclization of norephdrine derived α-iodoamides: synthesis of enantiopure pyrrolidines and trandition state modelling1 Tetrahedron. 48: 3945-3960. DOI: 10.1016/S0040-4020(01)88474-X |
0.421 |
|
| 1992 |
Bernardi A, Dotti P, Poli G, Scolastico C. Stereoselective Michael additions of titanium “ate” complexes of ketone and ester enolates Tetrahedron. 48: 5597-5606. DOI: 10.1016/0040-4020(92)80010-D |
0.448 |
|
| 1992 |
Chiari M, Micheletti C, Righetti PG, Poli G. Polyacrylamide gel polymerization under non-oxidizing conditions, as monitored by capillary zone electrophoresis Journal of Chromatography A. 598: 287-297. DOI: 10.1016/0021-9673(92)85058-2 |
0.337 |
|
| 1991 |
Bernardi A, Poli G, Scolastico C, Zanda M. Addition of racemic alkoxyallylstannanes to an enantiomerically pure 2-methoxyoxazolidine: an example of combined mutual diastereoface selection and kinetic resolution The Journal of Organic Chemistry. 56: 6961-6963. DOI: 10.1021/Jo00025A001 |
0.354 |
|
| 1991 |
Gennari C, Poli G, Scolastico C, Vassallo M. Stereoselective radical-mediated cyclization of norephedrine derived α-iodoamides: Experiments and TS-modelling Tetrahedron: Asymmetry. 2: 793-796. DOI: 10.1016/S0957-4166(00)80462-0 |
0.367 |
|
| 1991 |
Bernardi A, Carugo O, Pasquarello A, Sidjimov A, Poli G. Asymmetric hydrogenation of 3-methyl-fumaric and maleic ester monoaldehydes protected as neph-derived oxazolidines Tetrahedron. 47: 7357-7362. DOI: 10.1016/S0040-4020(01)89738-6 |
0.343 |
|
| 1991 |
Bernardi A, Cavicchioli M, Poli G, Scolastico C, Sidjimov A. Highly stereoselective acetylations via norephedrine derived oxazolidines. Tetrahedron. 47: 7925-7936. DOI: 10.1016/S0040-4020(01)81947-5 |
0.445 |
|
| 1990 |
Pasquarello A, Poli G, Potenza D, Scolastico C. Stereoconvergent crotylstannane addition to nor-ephedrine-derived 2-methoxy oxazolidines. A clue towards a synclinal transition state geometry Tetrahedron: Asymmetry. 1: 429-432. DOI: 10.1016/S0957-4166(00)86345-4 |
0.412 |
|
| 1990 |
Palazzi C, Poli G, Scolastico C, Villa R. Electrophilic α-formylation of carbonyl compounds using nor-ephedrine-derived 2-metohoxy oxazolidines. A novel asymmetric formation of quaternary stereocenters Tetrahedron Letters. 31: 4223-4226. DOI: 10.1016/S0040-4039(00)97587-7 |
0.419 |
|
| 1989 |
Oppolzer W, Kingma AJ, Poli G. Asymmetric 1,4-additions of gilman reagents to α,β - disubstitoted (e)-enoylsultams / "enolate" protonations Tetrahedron. 45: 479-488. DOI: 10.1016/0040-4020(89)80075-4 |
0.437 |
|
| 1989 |
OPPOLZER W, DUPUIS D, POLI G, RAYNHAM TM, BERNARDINELLI G. ChemInform Abstract: Enantioselective Synthesis and Absolute Configuration of (-)-Pulo′upone by Asymmetric Intramolecular Diels-Alder Reaction. Cheminform. 20. DOI: 10.1002/CHIN.198920299 |
0.407 |
|
| 1989 |
CARDANI S, POLI G, SCOLASTICO C, VILLA R. ChemInform Abstract: Allylic Stereocenter Directed Asymmetric Conjugate Addition of Cuprates in the Presence of Trimethylchlorosilane. Enantioselective Synthesis of 2-Alkyl-4-benzyloxybutanal and 2-Alkyl-4-oxopentanal. Cheminform. 20. DOI: 10.1002/CHIN.198904140 |
0.405 |
|
| 1988 |
Bernardi A, Cardani S, Pilati T, Poli G, Scolastico C, Villa R. Norephedrine-derived 2-alkenyloxazolidines: stereochemistry of cyclization and allylic stereocenter directed asymmetric conjugate addition The Journal of Organic Chemistry. 53: 1600-1607. DOI: 10.1021/Jo00243A002 |
0.486 |
|
| 1988 |
Oppolzer W, Dupuis D, Poli G, Raynham TM, Bernardinelli G. Enantioselective synthesis and absolute configuration of (-)-pulo'upone by asymmetric intramolecular diels-alder reaction Tetrahedron Letters. 29: 5885-5888. DOI: 10.1016/S0040-4039(00)82216-9 |
0.397 |
|
| 1988 |
Cardani S, Poli G, Scolastico C, Villa R. Allylic stereocenter directed asymmetric conjugate addition of cuprates in the presence of trimethylchlorosilane. enantioselective synthesis of 2-alkyl-4-benzyioxybutanal and 2-alkyl-4-oxopentanal Tetrahedron. 44: 5929-5938. DOI: 10.1016/S0040-4020(01)81451-4 |
0.479 |
|
| 1988 |
Oppolzer W, Poli G, Starkemann C, Bernardinelli G. Stable and reactive conformations of N-enoyl-bornane-10.2-sultams in the absence of lewis acids : asymmetric 1.4-hydride additions Tetrahedron Letters. 29: 3559-3562. DOI: 10.1016/0040-4039(88)85292-4 |
0.362 |
|
| 1988 |
BERNARDI A, CARDANI S, PILATI T, POLI G, SCOLASTICO C, VILLA R. ChemInform Abstract: Norephedrine-Derived 2-Alkenyloxazolidines: Stereochemistry of Cyclization and Allylic Stereocenter Directed Asymmetric Conjugate Addition. Cheminform. 19. DOI: 10.1002/CHIN.198840168 |
0.387 |
|
| 1987 |
Bernardi A, Cardani S, Colombo L, Poli G, Schimperna G, Scolastico C. Magnesium bromide-promoted addition of heterosubstituted methylketene silyl acetals to alkoxy aldehydes. Diastereoselective synthesis of 3,4-syn-2-methylene- and 2-(alkoxymethyl)-3-hydroxy-4-alkoxy esters The Journal of Organic Chemistry. 52: 888-891. DOI: 10.1021/Jo00381A029 |
0.498 |
|
| 1987 |
Banfi L, Cabri W, Poli G, Potenza D, Scolastico C. Absolute configuration of A-32'287 [conocandin] and total synthesis of its methyl and tert-butyl esters The Journal of Organic Chemistry. 52: 5452-5457. DOI: 10.1021/Jo00233A028 |
0.302 |
|
| 1987 |
Oppolzer W, Poli G, Kingma AJ, Starkemann C, Bernardinelli G. Asymmetric Induction at C(?) and C(?) ofN-Enoylsultams by Organomagnesium 1,4-Addition/Enolate Trapping Helvetica Chimica Acta. 70: 2201-2214. DOI: 10.1002/Hlca.19870700825 |
0.357 |
|
| 1987 |
BERNARDI A, CARDANI S, COLOMBO L, POLI G, SCHIMPERNA G, SCOLASTICO C. ChemInform Abstract: MgBr2-Promoted Addition of Heterosubstituted Methyl Ketene Silyl Acetals to Alkoxy Aldehydes. Diastereoselective Synthesis of 3,4-syn-2-Methylene- and 2-(Alkoxymethyl)-3-hydroxy-4-alkoxy Esters. Cheminform. 18. DOI: 10.1002/CHIN.198741102 |
0.322 |
|
| 1987 |
BERNARDI A, CARDANI S, POLI G, SCOLASTICO C. ChemInform Abstract: Allylic Stereocenter Directed Asymmetric Conjugate Addition. Enantioselective Synthesis of 3-Alkylsuccinaldehydic Acid Methyl Esters. Cheminform. 18. DOI: 10.1002/CHIN.198730147 |
0.319 |
|
| 1986 |
Kritchevsky D, Poli G, Scolastico C, Sirtori CR. Novel derivatives of 3α,7α-dihydroxy-5β-cholan-24-OIC acid (chenodeoxycholic acid) and 3α,7β-dihydroxy-5β-cholan-24-OIC acid (ursodeoxycholic acid) Steroids. 47: 41-48. PMID 3810698 DOI: 10.1016/0039-128X(86)90075-9 |
0.349 |
|
| 1986 |
Bernardi A, Cardani S, Poli G, Scolastico C. Allylic stereocenter directed asymmetric conjugate addition. Enantioselective synthesis of 3-alkylsuccinaldehydic acid methyl esters The Journal of Organic Chemistry. 51: 5041-5043. DOI: 10.1021/Jo00375A064 |
0.343 |
|
| 1986 |
Oppolzer W, Poli G. Asymmetric induction at C(β) and C(α) of N-enoyl sultams by 1,4-hydride addition/enolate trapping Tetrahedron Letters. 27: 4717-4720. DOI: 10.1016/S0040-4039(00)85046-7 |
0.338 |
|
| 1986 |
BERNARDI A, CABRI W, POLI G, PRATI L. ChemInform Abstract: Synthesis of (E)-7-Methyltridec-6-en-1-ol: A Comparative Study on the Stereoselective Synthesis of E-Trisubstituted Double Bonds. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198633308 |
0.328 |
|
| 1986 |
BERNARDI A, BERETTA MG, COLOMBO L, GENNARI C, POLI G, SCOLASTICO C. ChemInform Abstract: Synthetic Opportunities Offered by Anti α-Methylene-β-hydroxy-γ-alkoxy Esters: Stereoselective Reactions at the Double Bond. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198618201 |
0.429 |
|
| 1985 |
Annunziata R, Cinquini M, Cozzi F, Gilardi A, Cardani S, Poli G, Scolastico C. Double stereoselection in the aldol-type synthesis of γ-methyl and γ-alkoxy β-hydroxy ketones mediated by α-sulphinyl hydrazones Journal of the Chemical Society-Perkin Transactions 1. 16: 255-259. DOI: 10.1039/P19850000255 |
0.458 |
|
| 1985 |
Annunziata R, Cozzi F, Cinquini M, Colombo L, Gennari C, Poli G, Scolastico C. Chiral α-sulphinyl hydrazones as effective reagents for stereoselective aldol-type condensation Journal of the Chemical Society-Perkin Transactions 1. 16: 251-254. DOI: 10.1039/P19850000251 |
0.394 |
|
| 1985 |
Bernardi A, Beretta MG, Colombo L, Gennari C, Poli G, Scolastico C. Synthetic opportunities offered by anti .alpha.-methylene-.beta.-hydroxy-.gamma.-alkoxy esters: stereoselective reactions at the double bond The Journal of Organic Chemistry. 50: 4442-4447. DOI: 10.1021/Jo00223A005 |
0.35 |
|
| 1985 |
Bernardi A, Cardani S, Gennari C, Poli G, Scolastico C. Lewis acid promoted aldol additions of α-thiosilylketeneacetals to α-alkoxy aldehydes: diastereoselective synthesis of -α-methylene-β-hydroxy-∂-alkoxy esters. Tetrahedron Letters. 26: 6509-6512. DOI: 10.1016/S0040-4039(00)99039-7 |
0.361 |
|
| 1985 |
Colombo L, Gennari C, Poli G, Scolastico C, De Munari S. Asymetric dihydroxylations via chiral oxazolidines Tetrahedron Letters. 26: 5459-5462. DOI: 10.1016/S0040-4039(00)98236-4 |
0.407 |
|
| 1985 |
Gennari C, Bernardi A, Poli G, Scolastico C. Stereoselective aldol additions to α-alkoxy aldehydes using thioester silyl ketene acetals, Tetrahedron Letters. 26: 2373-2376. DOI: 10.1016/S0040-4039(00)95102-5 |
0.398 |
|
| 1985 |
GENNARI C, BERNARDI A, POLI G, SCOLASTICO C. ChemInform Abstract: STEREOSELECTIVE ALDOL ADDITIONS TO α-ALKOXY ALDEHYDES USING THIOESTER SILYL KETENE ACETALS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198534190 |
0.308 |
|
| 1984 |
Gennari C, Colombo L, Poli G. Enolboronates: New practical reagents for regioselective aldol condensations. Tetrahedron Letters. 25: 2279-2282. DOI: 10.1016/S0040-4039(01)80232-X |
0.423 |
|
| 1983 |
Colombo L, Gennari C, Poli G, Scolastico C, Aragozzini F, Merendi C. Biosynthesis of austdiol and synthesis of a deuterium labelled biogenetic precursor Journal of the Chemical Society-Perkin Transactions 1. 15: 2745-2749. DOI: 10.1039/P19830002745 |
0.346 |
|
| 1983 |
Colombo L, Gennari C, Poli G, Scolastico C, Annunziata R, Cinquini M, Cozzi F. Enantionselective aldol-type condensation mediated by chiral α-sulphinyl hydrazones Journal of the Chemical Society, Chemical Communications. 403-404. DOI: 10.1039/C39830000403 |
0.405 |
|
| 1983 |
COLUMBO L, GENNARI C, POLI G, SCOLASTICO C, ANNUNZIATA R, CINQUINI M, COZZI F. ChemInform Abstract: Enantioselective Aldol-Type Condensation Mediated by Chiral α-Sulphinyl Hydrazones. Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198332156 |
0.374 |
|
| 1982 |
Colombo L, Gennari C, Poli G, Scolastico C. Enantioselective synthesis of secondary alcohols in the presence of chiral ligands Tetrahedron. 38: 2725-2727. DOI: 10.1016/0040-4020(82)80029-X |
0.472 |
|
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