| Year |
Citation |
Score |
| 2023 |
Patel K, Oginetz L, Marek I. Highly Diastereoselective Preparation of Tertiary Alkyl Thiocyanates en Route to Thiols by Stereoinvertive Nucleophilic Substitution at Nonclassical Carbocations. Organic Letters. 25: 8474-8477. PMID 37982581 DOI: 10.1021/acs.orglett.3c03396 |
0.454 |
|
| 2023 |
Chen X, Marek I. Highly Diastereoselective Preparation of Tertiary Alkyl Isonitriles by Stereoinvertive Nucleophilic Substitution at a Nonclassical Carbocation. Organic Letters. PMID 36976777 DOI: 10.1021/acs.orglett.3c00583 |
0.485 |
|
| 2022 |
Myronova V, Cahard D, Marek I. Stereoselective Preparation of CF-Containing Cyclopropanes. Organic Letters. 24: 9076-9080. PMID 36456393 DOI: 10.1021/acs.orglett.2c03714 |
0.323 |
|
| 2022 |
Pavlíčková T, Stöckl Y, Marek I. Synthesis and Functionalization of Tertiary Propargylic Boronic Esters by Alkynyllithium-Mediated 1,2-Metalate Rearrangement of Borylated Cyclopropanes. Organic Letters. 24: 8901-8906. PMID 36446049 DOI: 10.1021/acs.orglett.2c03756 |
0.364 |
|
| 2022 |
Chen X, Patel K, Marek I. Stereoselective Construction of Tertiary Homoallyl Alcohols and Ethers by Nucleophilic Substitution at Quaternary Carbon Stereocenter. Angewandte Chemie (International Ed. in English). PMID 36413111 DOI: 10.1002/anie.202212425 |
0.351 |
|
| 2022 |
Cohen A, Siddaraju Y, Marek I. Directed Diastereoselective Cyclopropanation and Epoxidation of Alkenyl Cyclopropyl Carbinol Derivatives. Organic Letters. 24: 8322-8325. PMID 36354275 DOI: 10.1021/acs.orglett.2c03305 |
0.456 |
|
| 2022 |
Cohen Y, Marek I. Regio- and Diastereoselective Carbometalation Reaction of Cyclopropenes. Accounts of Chemical Research. PMID 36102664 DOI: 10.1021/acs.accounts.2c00424 |
0.501 |
|
| 2022 |
Cohen Y, Toledano D, Marek I. Stereoselective Synthesis of Polysubstituted Spiropentanes. Journal of the American Chemical Society. PMID 36088586 DOI: 10.1021/jacs.2c07370 |
0.316 |
|
| 2022 |
Augustin AU, Di Silvio S, Marek I. Borylated Cyclopropanes as Spring-Loaded Entities: Access to Vicinal Tertiary and Quaternary Carbon Stereocenters in Acyclic Systems. Journal of the American Chemical Society. PMID 36041738 DOI: 10.1021/jacs.2c07394 |
0.794 |
|
| 2022 |
Siddaraju Y, Sabbatani J, Cohen A, Marek I. Preparation of Distant Quaternary Carbon Stereocenters by Double Selective Ring-Opening of 1,1-Biscyclopropyl Methanol Derivatives. Angewandte Chemie (International Ed. in English). e202203652. PMID 35521738 DOI: 10.1002/anie.202203652 |
0.412 |
|
| 2022 |
Chen X, Marek I. Stereoinvertive Nucleophilic Substitution at Quaternary Carbon Stereocenters of Cyclopropyl Ketones and Ethers. Angewandte Chemie (International Ed. in English). PMID 35471589 DOI: 10.1002/anie.202203673 |
0.421 |
|
| 2022 |
Patel K, Lanke V, Marek I. Stereospecific Construction of Quaternary Carbon Stereocenters from Quaternary Carbon Stereocenters. Journal of the American Chemical Society. PMID 35412821 DOI: 10.1021/jacs.2c01695 |
0.776 |
|
| 2022 |
Cohen A, Kaushansky A, Marek I. Mechanistic Insights on the Selectivity of the Tandem Heck-Ring-Opening of Cyclopropyldiol Derivatives. Jacs Au. 2: 687-696. PMID 35373195 DOI: 10.1021/jacsau.1c00547 |
0.415 |
|
| 2021 |
Marek I, Cohen Y. Directed Regioselective Carbometallation of 1,2-Dialkyl-Substituted Cyclopropenes. Angewandte Chemie (International Ed. in English). PMID 34617656 DOI: 10.1002/anie.202111382 |
0.367 |
|
| 2021 |
Wang PY, Massad I, Marek I. Stereoselective Sc(OTf) -Catalyzed Aldol Reactions of Disubstituted Silyl Enol Ethers of Aldehydes with Acetals. Angewandte Chemie (International Ed. in English). 60: 12765-12769. PMID 33779017 DOI: 10.1002/anie.202101634 |
0.418 |
|
| 2021 |
Marek I, Cohen Y, Augustin AU, Levy L, Jones PG, Werz DB. Regio- and Diastereoselective Copper-Catalyzed Carbomagnesiation for the Synthesis of Penta- and Hexa-Substituted Cyclopropanes. Angewandte Chemie (International Ed. in English). PMID 33742749 DOI: 10.1002/anie.202102509 |
0.842 |
|
| 2020 |
Lanke V, Marek I. Stereospecific nucleophilic substitution at tertiary and quaternary stereocentres. Chemical Science. 11: 9378-9385. PMID 34094203 DOI: 10.1039/d0sc02562c |
0.8 |
|
| 2020 |
Ho GM, Segura L, Marek I. Ru-catalyzed isomerization of ω-alkenylboronates towards stereoselective synthesis of vinylboronates with subsequent functionalization. Chemical Science. 11: 5944-5949. PMID 34094086 DOI: 10.1039/d0sc02542a |
0.387 |
|
| 2020 |
Dian L, Marek I. Pd-Catalyzed Enantioselective Hydroalkynylation of Cyclopropenes. Acs Catalysis. 10: 1289-1293. PMID 32953232 DOI: 10.1021/Acscatal.9B04960 |
0.776 |
|
| 2020 |
Marek I, Zhang FG, Wang XQ, Zhou Y, Shi HS, Feng Z, Ma JA. Remote Fluorination and Fluoroalkyl(thiol)ation Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32779797 DOI: 10.1002/Chem.202003416 |
0.411 |
|
| 2020 |
Marek I, Pierrot D. Stereospecific Access to Allylboronic Esters Within Acyclic Systems Bearing Distant Tetrasubstituted Stereocenters. Angewandte Chemie (International Ed. in English). PMID 32757448 DOI: 10.1002/Anie.202010135 |
0.466 |
|
| 2020 |
Cohen Y, Cohen A, Marek I. Creating Stereocenters within Acyclic Systems by C-C Bond Cleavage of Cyclopropanes. Chemical Reviews. PMID 32657576 DOI: 10.1021/Acs.Chemrev.0C00167 |
0.415 |
|
| 2020 |
Dian L, Marek I. Cobalt-Catalyzed Diastereoselective and Enantioselective Hydrosilylation of Achiral Cyclopropenes. Organic Letters. 22: 4914-4918. PMID 32506912 DOI: 10.1021/Acs.Orglett.0C01833 |
0.837 |
|
| 2020 |
Marek I, Massad I, Sommer H. Stereoselective Access to Fully Substituted Aldehyde Silyl Enol Ethers by Iridium-Catalyzed Alkene Isomerization. Angewandte Chemie (International Ed. in English). PMID 32392394 DOI: 10.1002/Anie.202005058 |
0.513 |
|
| 2020 |
Lanke V, Marek I. Correction to "Nucleophilic Substitution at Quaternary Carbon Stereocenters". Journal of the American Chemical Society. 142: 7710-7712. PMID 32274924 DOI: 10.1021/Jacs.0C03380 |
0.78 |
|
| 2020 |
Lanke V, Marek I. Nucleophilic Substitution at Quaternary Carbon Stereocenters. Journal of the American Chemical Society. PMID 32141750 DOI: 10.1021/Jacs.0C01133 |
0.814 |
|
| 2020 |
Lanke V, Marek I. Stereospecific nucleophilic substitution at tertiary and quaternary stereocentres Chemical Science. 11: 9378-9385. DOI: 10.1039/D0Sc02562C |
0.806 |
|
| 2020 |
Ho G, Segura L, Marek I. Ru-catalyzed isomerization of ω-alkenylboronates towards stereoselective synthesis of vinylboronates with subsequent in situ functionalization Chemical Science. 11: 5944-5949. DOI: 10.1039/D0Sc02542A |
0.49 |
|
| 2020 |
Cohen A, Chagneau J, Marek I. Stereoselective Preparation of Distant Stereocenters (1,5) within Acyclic Molecules Acs Catalysis. 10: 7154-7161. DOI: 10.1021/Acscatal.0C01762 |
0.315 |
|
| 2020 |
Massad I, Marek I. Alkene Isomerization through Allylmetals as a Strategic Tool in Stereoselective Synthesis Acs Catalysis. 10: 5793-5804. DOI: 10.1021/Acscatal.0C01174 |
0.377 |
|
| 2020 |
Huang J, Marek I. Construction of Acyclic Vicinal Tertiary and Quaternary Carbon Stereocenters via a Pd‐Catalyzed Allylic Alkylation of Stereodefined Polysubstituted Ketene Aminals European Journal of Organic Chemistry. 2020: 3133-3137. DOI: 10.1002/Ejoc.201901741 |
0.458 |
|
| 2020 |
Pierrot D, Marek I. Synthese enantiomerenangereicherter, vicinaler tertiärer und quartärer Kohlenstoff‐Stereozentren innerhalb einer acyclischen Kette Angewandte Chemie. 132: 36-49. DOI: 10.1002/Ange.201903188 |
0.345 |
|
| 2019 |
Sommer H, Weissbrod T, Marek I. A Tandem Iridium-Catalyzed "Chain-Walking"/Cope Rearrangement Sequence. Acs Catalysis. 9: 2400-2406. PMID 32953237 DOI: 10.1021/Acscatal.9B00118 |
0.49 |
|
| 2019 |
Lanke V, Zhang FG, Kaushansky A, Marek I. Diastereoselective ring opening of fully-substituted cyclopropanes intramolecular Friedel-Crafts alkylation. Chemical Science. 10: 9548-9554. PMID 32055326 DOI: 10.1039/C9Sc03832A |
0.796 |
|
| 2019 |
Cohen Y, Marek I. Regio- and Diastereoselective Copper-Catalyzed Carbometalation of Cyclopropenylsilanes. Organic Letters. PMID 31674787 DOI: 10.1021/Acs.Orglett.9B03531 |
0.436 |
|
| 2019 |
Zhang ZQ, Zheng MM, Xue XS, Marek I, Zhang FG, Ma JA. Catalytic Enantioselective Cyclopropenation of Internal Alkynes: Access to Difluoromethylated Three-Membered Carbocycles. Angewandte Chemie (International Ed. in English). PMID 31633856 DOI: 10.1002/Anie.201911701 |
0.494 |
|
| 2019 |
Marek I. Regio- and Stereoselective Synthesis of Fully Substituted Silyl Enol Ethers of Ketones and Aldehydes in Acyclic Systems. Angewandte Chemie (International Ed. in English). PMID 31424601 DOI: 10.1002/Anie.201909089 |
0.516 |
|
| 2019 |
Marek I, Pierrot D. Synthesis of Enantioenriched Vicinal Tertiary and Quaternary Carbon Stereogenic Centers Within an Acyclic Chain. Angewandte Chemie (International Ed. in English). PMID 31081180 DOI: 10.1002/Anie.201903188 |
0.423 |
|
| 2019 |
Simaan M, Marek I. Diastereo- and enantioselective preparation of cyclopropanol derivatives. Beilstein Journal of Organic Chemistry. 15: 752-760. PMID 30992723 DOI: 10.3762/Bjoc.15.71 |
0.493 |
|
| 2019 |
Ho GM, Sommer H, Marek I. Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers. Organic Letters. PMID 30942604 DOI: 10.1021/Acs.Orglett.9B00946 |
0.459 |
|
| 2019 |
Marek I. Synthesis and Reactivity of sp(2) Geminated Organobismetallic Derivatives. Chemical Reviews. 100: 2887-900. PMID 11749308 DOI: 10.1021/Cr990288E |
0.408 |
|
| 2019 |
Zhang Z, Zheng M, Xue X, Marek I, Zhang F, Ma J. Back Cover: Catalytic Enantioselective Cyclopropenation of Internal Alkynes: Access to Difluoromethylated Three‐Membered Carbocycles (Angew. Chem. Int. Ed. 50/2019) Angewandte Chemie. 58: 18298-18298. DOI: 10.1002/Anie.201913897 |
0.384 |
|
| 2019 |
Zhang Z, Zheng M, Xue X, Marek I, Zhang F, Ma J. Rücktitelbild: Catalytic Enantioselective Cyclopropenation of Internal Alkynes: Access to Difluoromethylated Three‐Membered Carbocycles (Angew. Chem. 50/2019) Angewandte Chemie. 131: 18464-18464. DOI: 10.1002/Ange.201913897 |
0.409 |
|
| 2018 |
Sommer H, Marek I. Diastereo- and enantioselective copper catalyzed hydroallylation of disubstituted cyclopropenes. Chemical Science. 9: 6503-6508. PMID 30310580 DOI: 10.1039/C8Sc02085J |
0.478 |
|
| 2018 |
Marek I, Tugny C, Zhang FG. Versatility in the Brook Rearrangement for the Selective Ring-Opening of Three-Membered Rings. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30294820 DOI: 10.1002/Chem.201805006 |
0.399 |
|
| 2018 |
Dian L, Marek I. Asymmetric Preparation of Polysubstituted Cyclopropanes Based on Direct Functionalization of Achiral Three-Membered Carbocycles. Chemical Reviews. PMID 30156832 DOI: 10.1021/Acs.Chemrev.8B00304 |
0.817 |
|
| 2018 |
Bruffaerts J, Pierrot D, Marek I. Efficient and stereodivergent synthesis of unsaturated acyclic fragments bearing contiguous stereogenic elements. Nature Chemistry. PMID 30150723 DOI: 10.1038/S41557-018-0123-7 |
0.456 |
|
| 2018 |
Marek I, Cormier M, de la Torre A. Total Synthesis of C30 Botryococcene and epi-Botryococcene via a Diastereoselective Ring Opening of Alkenylcyclopropanes. Angewandte Chemie (International Ed. in English). PMID 30134044 DOI: 10.1002/Anie.201808709 |
0.79 |
|
| 2018 |
Marek I, Ho GM, Judkele L, Bruffaerts J. Metal-Catalyzed Remote Functionalization of ω-Ene Unsaturated Ethers as A New Entry to Functionalized Vinyl Species. Angewandte Chemie (International Ed. in English). PMID 29744998 DOI: 10.1002/Anie.201802434 |
0.422 |
|
| 2018 |
Marek I, Singh S, Simaan M. Pd-Catalyzed Selective Remote Ring Opening of Polysubstituted Cyclopropanols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29694690 DOI: 10.1002/Chem.201802016 |
0.425 |
|
| 2018 |
Bruffaerts J, Vasseur A, Singh S, Masarwa A, Didier D, Oskar L, Perrin L, Eisenstein O, Marek I. Zirconocene-Mediated Selective C-C Bond Cleavage of Strained Carbocycles: Scope and Mechanism. The Journal of Organic Chemistry. PMID 29537856 DOI: 10.1021/Acs.Joc.7B03115 |
0.378 |
|
| 2018 |
Sommer H, Juliá-Hernández F, Martin R, Marek I. Walking Metals for Remote Functionalization. Acs Central Science. 4: 153-165. PMID 29532015 DOI: 10.1021/Acscentsci.8B00005 |
0.309 |
|
| 2018 |
Marek I, Dian L. Rh-Catalyzed Arylation of Cyclopropenes Based on Asymmetric Directed Functionalization of Three-Membered Carbocycles. Angewandte Chemie (International Ed. in English). PMID 29446194 DOI: 10.1002/Anie.201713324 |
0.828 |
|
| 2018 |
Huang JQ, Nairoukh Z, Marek I. Electrophilic fluorination of stereodefined disubstituted silyl ketene hemiaminals en route to tertiary α-fluorinated carbonyl derivatives. Organic & Biomolecular Chemistry. PMID 29368785 DOI: 10.1039/C8Ob00067K |
0.502 |
|
| 2018 |
Simaan M, Marek I. Asymmetric Catalytic Preparation of Polysubstituted Cyclopropanol and Cyclopropylamine Derivatives. Angewandte Chemie (International Ed. in English). PMID 29320599 DOI: 10.1002/Anie.201710707 |
0.48 |
|
| 2018 |
Bruffaerts J, Pierrot D, Marek I. Zirconocene-assisted remote cleavage of C-C and C-O bonds: application to acyclic stereodefined metalated hydrocarbons. Organic & Biomolecular Chemistry. 14: 10325-10330. PMID 27782275 DOI: 10.1039/C6Ob01910B |
0.309 |
|
| 2018 |
Shterenberg A, Haimov E, Smirnov P, Marek I. Convergent and flexible approach to stereodefined polyhydroxylated fragments Tetrahedron. 74: 6761-6768. DOI: 10.1016/J.Tet.2018.10.013 |
0.446 |
|
| 2018 |
Marek I. Rosarium Philosophorum on Organic Synthesis Israel Journal of Chemistry. 58: 122-126. DOI: 10.1002/Ijch.201700135 |
0.324 |
|
| 2018 |
Bruffaerts J, Vasseur A, Marek I. Alkene‐Zipper Catalyzed Selective and Remote Retro‐ene Reaction of Alkenyl Cyclopropylcarbinol Advanced Synthesis & Catalysis. 360: 1389-1396. DOI: 10.1002/Adsc.201701481 |
0.442 |
|
| 2017 |
Müller DS, Werner V, Akyol S, Schmalz HG, Marek I. Tandem Hydroalumination/Cu-Catalyzed Asymmetric Vinyl Metalation as a New Access to Enantioenriched Vinylcyclopropane Derivatives. Organic Letters. PMID 28741951 DOI: 10.1021/Acs.Orglett.7B01661 |
0.436 |
|
| 2017 |
Starkov P, Moore JT, Duquette DC, Stoltz BM, Marek I. Enantioselective Construction of Acyclic Quaternary Carbon Stereocen-ters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully-Substituted Amide Enolates. Journal of the American Chemical Society. PMID 28625056 DOI: 10.1021/Jacs.7B04086 |
0.56 |
|
| 2017 |
Zhang FG, Marek I. Brook Rearrangement as a Trigger for the Formation of Carbene: Formation of Stereodefined Fully-Substituted Cyclobutene Derivatives. Journal of the American Chemical Society. PMID 28571310 DOI: 10.1021/Jacs.7B04255 |
0.565 |
|
| 2017 |
Dian L, Müller DS, Marek I. Asymmetric Copper-Catalyzed Carbomagnesiation of Cyclopropenes. Angewandte Chemie (International Ed. in English). PMID 28504482 DOI: 10.1002/Anie.201701094 |
0.823 |
|
| 2017 |
Nairoukh Z, Kumar GGKSN, Minko Y, Marek I. Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres. Chemical Science. 8: 627-630. PMID 28451210 DOI: 10.1039/C6Sc03036J |
0.518 |
|
| 2017 |
Roy SR, Eijsberg H, Bruffaerts J, Marek I. Zirconocene catalyzed diastereoselective carbometalation of cyclobutenes. Chemical Science. 8: 334-339. PMID 28451177 DOI: 10.1039/C6Sc02617F |
0.628 |
|
| 2017 |
Singh S, Bruffaerts J, Vasseur A, Marek I. A unique Pd-catalysed Heck arylation as a remote trigger for cyclopropane selective ring-opening. Nature Communications. 8: 14200. PMID 28169276 DOI: 10.1038/Ncomms14200 |
0.447 |
|
| 2017 |
Vasseur A, Marek I. Merging allylic C-H bond activation and C-C bond cleavage en route to the formation of a quaternary carbon stereocenter in acyclic systems. Nature Protocols. 12: 74-87. PMID 27929522 DOI: 10.1038/Nprot.2016.161 |
0.458 |
|
| 2017 |
Huang JQ, Nairoukh Z, Marek I. Electrophilic Oxidation of Stereodefined Polysubstituted Silyl Ketone Aminals European Journal of Organic Chemistry. 2018: 614-618. DOI: 10.1002/Ejoc.201701516 |
0.317 |
|
| 2016 |
Roy SR, Didier D, Kleiner A, Marek I. Diastereodivergent combined carbometalation/zinc homologation/C-C fragmentation reaction as an efficient tool to prepare acyclic allylic quaternary carbon stereocenters. Chemical Science. 7: 5989-5994. PMID 30034740 DOI: 10.1039/C6Sc02191C |
0.801 |
|
| 2016 |
Cao B, Simaan M, Marek I, Wei Y, Shi M. Palladium-catalyzed oxidative cyclization of aniline-tethered alkylidenecyclopropanes with O2: a facile protocol to selectively synthesize 2- and 3-vinylindoles. Chemical Communications (Cambridge, England). PMID 27918016 DOI: 10.1039/C6Cc08731K |
0.438 |
|
| 2016 |
Müller DS, Marek I. Correction to "Asymmetric Copper-Catalyzed Carbozincation of Cyclopropenes en Route to the Formation of Diastereo- and Enantiomerically Enriched Polysubstituted Cyclopropanes". Journal of the American Chemical Society. 138: 14503. PMID 27802601 DOI: 10.1021/jacs.6b08103 |
0.349 |
|
| 2016 |
Leibeling M, Shurrush KA, Werner V, Perrin L, Marek I. Preparation and Reactivity of Acyclic Chiral Allylzinc Species by a Zinc-Brook Rearrangement. Angewandte Chemie (International Ed. in English). PMID 27061357 DOI: 10.1002/Anie.201602393 |
0.46 |
|
| 2016 |
Haimov E, Nairoukh Z, Shterenberg A, Berkovitz T, Jamison TF, Marek I. Stereoselective Formation of Fully Substituted Ketone Enolates. Angewandte Chemie (International Ed. in English). PMID 27027778 DOI: 10.1002/Anie.201601883 |
0.512 |
|
| 2016 |
Vasseur A, Bruffaerts J, Marek I. Remote functionalization through alkene isomerization. Nature Chemistry. 8: 209-19. PMID 26892551 DOI: 10.1038/Nchem.2445 |
0.421 |
|
| 2016 |
Preshel-Zlatsin M, Zhang FG, Eppe G, Marek I. Formation of Carbon Quaternary Stereogenic Center in Acyclic Systems via a Sequence of Carbometalation-Intramolecular Cyclization-Silicon Activation Synthesis (Germany). 48: 3279-3286. DOI: 10.1055/S-0035-1561666 |
0.512 |
|
| 2016 |
Roy SR, Didier D, Kleiner A, Marek I. Diastereodivergent combined carbometalation/zinc homologation/C-C fragmentation reaction as an efficient tool to prepare acyclic allylic quaternary carbon stereocenters Chemical Science. 7: 5989-5994. DOI: 10.1039/c6sc02191c |
0.674 |
|
| 2016 |
Müller DS, Marek I. Copper mediated carbometalation reactions Chemical Society Reviews. 45: 4552-4566. DOI: 10.1039/C5Cs00897B |
0.436 |
|
| 2015 |
Li DY, Wei Y, Marek I, Tang XY, Shi M. Gold(i)-catalyzed cycloisomerization of vinylidenecyclopropane-enes carbene or non-carbene processes. Chemical Science. 6: 5519-5525. PMID 29861890 DOI: 10.1039/C5Sc01806D |
0.41 |
|
| 2015 |
Vasseur A, Perrin L, Eisenstein O, Marek I. Remote functionalization of hydrocarbons with reversibility enhanced stereocontrol. Chemical Science. 6: 2770-2776. PMID 29142680 DOI: 10.1039/C5Sc00445D |
0.343 |
|
| 2015 |
Zhang FG, Eppe G, Marek I. Brook Rearrangement as a Trigger for the Ring Opening of Strained Carbocycles. Angewandte Chemie (International Ed. in English). PMID 26663399 DOI: 10.1002/Anie.201510094 |
0.471 |
|
| 2015 |
Müller DS, Marek I. Asymmetric Copper-Catalyzed Carbozincation of Cyclopropenes en Route to the Formation of Diastereo- and Enantiomerically Enriched Polysubstituted Cyclopropanes. Journal of the American Chemical Society. PMID 26624801 DOI: 10.1021/Jacs.5B11220 |
0.51 |
|
| 2015 |
Masarwa A, Gerbig D, Oskar L, Loewenstein A, Reisenauer HP, Lesot P, Schreiner PR, Marek I. Synthesis and Stereochemical Assignment of Crypto-Optically Active (2) H6 -Neopentane. Angewandte Chemie (International Ed. in English). 54: 13106-9. PMID 26480341 DOI: 10.1002/Anie.201505349 |
0.378 |
|
| 2015 |
Nairoukh Z, Marek I. Stereodefined Acyclic Polysubstituted Silyl Ketene Aminals: Asymmetric Formation of Aldol Products with Quaternary Carbon Stereocenters. Angewandte Chemie (International Ed. in English). 54: 14393-7. PMID 26448575 DOI: 10.1002/Anie.201507209 |
0.516 |
|
| 2015 |
Vabre R, Island B, Diehl CJ, Schreiner PR, Marek I. Forming Stereogenic Centers in Acyclic Systems from Alkynes. Angewandte Chemie (International Ed. in English). 54: 9996-9. PMID 26130570 DOI: 10.1002/Anie.201504756 |
0.491 |
|
| 2015 |
Eppe G, Didier D, Marek I. Stereocontrolled Formation of Several Carbon-Carbon Bonds in Acyclic Systems. Chemical Reviews. 115: 9175-206. PMID 25768205 DOI: 10.1021/Cr500715T |
0.334 |
|
| 2015 |
Simaan M, Delaye PO, Shi M, Marek I. Cyclopropene Derivatives as Precursors to Enantioenriched Cyclopropanols and n-Butenals Possessing Quaternary Carbon Stereocenters. Angewandte Chemie (International Ed. in English). PMID 25689601 DOI: 10.1002/Anie.201412440 |
0.515 |
|
| 2015 |
Starkov P, Jamison TF, Marek I. Electrophilic amination: the case of nitrenoids. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5278-300. PMID 25641706 DOI: 10.1002/Chem.201405779 |
0.304 |
|
| 2015 |
Marek I, Masarwa A, Delaye PO, Leibeling M. Selective carbon-carbon bond cleavage for the stereoselective synthesis of acyclic systems. Angewandte Chemie (International Ed. in English). 54: 414-29. PMID 25266824 DOI: 10.1002/Anie.201405067 |
0.426 |
|
| 2015 |
Li DY, Wei Y, Marek I, Tang XY, Shi M. Gold(I)-catalyzed cycloisomerization of vinylidenecyclopropane-enes via carbene or non-carbene processes Chemical Science. 6: 5519-5525. DOI: 10.1039/c5sc01806d |
0.301 |
|
| 2015 |
Vincent G, Cheli S, Martinez Mallorquin R, Abramovitch A, Beauvière S, Gomez C, Brebion F, Marek I, Malacria M, Goddard JP, Fensterbank L. Oxidation of bis-sulfinyl carbanions as the pivot of ionic/radical tandem reactions Comptes Rendus Chimie. DOI: 10.1016/J.Crci.2015.11.012 |
0.394 |
|
| 2015 |
Zhu PL, Zhang Z, Tang XY, Marek I, Shi M. Gold- and silver-catalyzed intramolecular cyclizations of indolylcyclopropenes for the divergent synthesis of azepinoindoles and spiroindoline piperidines Chemcatchem. 7: 595-600. DOI: 10.1002/Cctc.201402940 |
0.426 |
|
| 2015 |
Sklute G, Cavender H, Marek I. Carbozincation Reactions of Carbon–Carbon Multiple Bonds Organic Reactions. 507-764. DOI: 10.1002/0471264180.Or087.03 |
0.465 |
|
| 2014 |
Smirnov P, Katan E, Mathew J, Kostenko A, Karni M, Nijs A, Bolm C, Apeloig Y, Marek I. Formation of three new bonds and two stereocenters in acyclic systems by zinc-mediated enantioselective alkynylation of acylsilanes, Brook rearrangement, and ene-allene carbocyclization reactions. The Journal of Organic Chemistry. 79: 12122-35. PMID 25271364 DOI: 10.1021/Jo501977R |
0.485 |
|
| 2014 |
Klier L, Diène CR, Schickinger M, Metzger A, Wagner AJ, Karaghiosoff K, Marek I, Knochel P. Isoxazole-embedded allylic zinc reagent for the diastereoselective preparation of highly functionalized aldol-type derivatives bearing a stereocontrolled quaternary center. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 14096-101. PMID 25204300 DOI: 10.1002/Chem.201402733 |
0.537 |
|
| 2014 |
Minko Y, Marek I. Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres. Chemical Communications (Cambridge, England). 50: 12597-611. PMID 25054432 DOI: 10.1039/C4Cc04391J |
0.473 |
|
| 2014 |
Marek I, Minko Y, Pasco M, Mejuch T, Gilboa N, Chechik H, Das JP. All-carbon quaternary stereogenic centers in acyclic systems through the creation of several C-C bonds per chemical step. Journal of the American Chemical Society. 136: 2682-94. PMID 24512113 DOI: 10.1021/Ja410424G |
0.415 |
|
| 2014 |
Shen ZL, Peng Z, Yang CM, Helberg J, Mayer P, Marek I, Knochel P. Highly diastereoselective preparation of aldol products using new functionalized allylic aluminum reagents. Organic Letters. 16: 956-9. PMID 24479467 DOI: 10.1021/Ol403692K |
0.571 |
|
| 2014 |
Minko Y, Marek I. Oxenoids in organic synthesis. Organic & Biomolecular Chemistry. 12: 1535-46. PMID 24477293 DOI: 10.1039/C3Ob42349B |
0.344 |
|
| 2014 |
Didier D, Delaye PO, Simaan M, Island B, Eppe G, Eijsberg H, Kleiner A, Knochel P, Marek I. Modulable and highly diastereoselective carbometalations of cyclopropenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1038-48. PMID 24338953 DOI: 10.1002/Chem.201303569 |
0.804 |
|
| 2014 |
Masarwa A, Didier D, Zabrodski T, Schinkel M, Ackermann L, Marek I. Merging allylic carbon-hydrogen and selective carbon-carbon bond activation. Nature. 505: 199-203. PMID 24317692 DOI: 10.1038/Nature12761 |
0.409 |
|
| 2014 |
Knochel P, Haas D, Masarwa A, Didier D, Zabrodski T, Schinkel M, Ackermann L, Marek I. Zirconium-Promoted Combined C–H and C–C Bond Activation Synfacts. 10: 417-417. DOI: 10.1055/S-0033-1340933 |
0.353 |
|
| 2014 |
Didier D, Delaye P, Simaan M, Island B, Eppe G, Eijsberg H, Kleiner A, Knochel P, Marek I. Cover Picture: Modulable and Highly Diastereoselective Carbometalations of Cyclopropenes (Chem. Eur. J. 4/2014) Chemistry - a European Journal. 20: 909-909. DOI: 10.1002/Chem.201490010 |
0.35 |
|
| 2013 |
Smirnov P, Mathew J, Nijs A, Katan E, Karni M, Bolm C, Apeloig Y, Marek I. One-pot zinc-promoted asymmetric alkynylation/brook-type rearrangement/ene-allene cyclization: highly selective formation of three new bonds and two stereocenters in acyclic systems. Angewandte Chemie (International Ed. in English). 52: 13717-21. PMID 24155160 DOI: 10.1002/Anie.201306749 |
0.432 |
|
| 2013 |
Schinkel M, Wallbaum J, Kozhushkov SI, Marek I, Ackermann L. Carboxylate assistance for catalyzed hydroarylations of methylenecyclopropanes. Organic Letters. 15: 4482-4. PMID 23957454 DOI: 10.1021/Ol402037F |
0.379 |
|
| 2013 |
Mejuch T, Gilboa N, Gayon E, Wang H, Houk KN, Marek I. Axial preferences in allylation reactions via the Zimmerman-Traxler transition state. Accounts of Chemical Research. 46: 1659-69. PMID 23672428 DOI: 10.1021/Ar4000532 |
0.475 |
|
| 2013 |
Minko Y, Pasco M, Chechik H, Marek I. Regio- and stereoselective carbometallation reactions of N-alkynylamides and sulfonamides. Beilstein Journal of Organic Chemistry. 9: 526-32. PMID 23616793 DOI: 10.3762/Bjoc.9.57 |
0.443 |
|
| 2013 |
Delaye PO, Didier D, Marek I. Diastereodivergent carbometalation/oxidation/selective ring opening: formation of all-carbon quaternary stereogenic centers in acyclic systems. Angewandte Chemie (International Ed. in English). 52: 5333-7. PMID 23589464 DOI: 10.1002/Anie.201300664 |
0.353 |
|
| 2013 |
Minko Y, Pasco M, Lercher L, Marek I. Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems. Nature Protocols. 8: 749-54. PMID 23518666 DOI: 10.1038/Nprot.2013.036 |
0.498 |
|
| 2013 |
Schinkel M, Marek I, Ackermann L. Carboxylate-assisted ruthenium(II)-catalyzed hydroarylations of unactivated alkenes through C-H cleavage. Angewandte Chemie (International Ed. in English). 52: 3977-80. PMID 23440879 DOI: 10.1002/Anie.201208446 |
0.301 |
|
| 2013 |
Beauvière S, Brebion F, Chelli S, Delouvrié B, Gomez C, Kwasnieski O, Mallorquin RM, Najera F, Vincent G, Vitale MR, Derat E, Marek I, Malacria M, Goddard JP, Fensterbank L. New advances in bis(sulfoxides) chemistry Phosphorus, Sulfur and Silicon and the Related Elements. 188: 367-376. DOI: 10.1080/10426507.2012.738739 |
0.365 |
|
| 2013 |
Pasco M, Gilboa N, Mejuch T, Marek I. The renaissance of zinc carbenoid in stereoselective synthesis in acyclic systems Organometallics. 32: 942-950. DOI: 10.1021/Om301220A |
0.533 |
|
| 2013 |
Diers E, Phani Kumar NY, Mejuch T, Marek I, Ackermann L. Carboxylate-assisted ruthenium(II)-catalyzed C-H arylations of 5-aryl tetrazoles: Step-economical access to Valsartan Tetrahedron. 69: 4445-4453. DOI: 10.1016/J.Tet.2013.01.006 |
0.384 |
|
| 2012 |
Minko Y, Pasco M, Lercher L, Botoshansky M, Marek I. Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes. Nature. 490: 522-6. PMID 23099407 DOI: 10.1038/Nature11569 |
0.477 |
|
| 2012 |
Mejuch T, Dutta B, Botoshansky M, Marek I. Convergent diastereoselective preparation of adjacent quaternary stereocenters in an acyclic system. Organic & Biomolecular Chemistry. 10: 5803-6. PMID 22402794 DOI: 10.1039/C2Ob25121C |
0.545 |
|
| 2011 |
Basheer A, Mishima M, Marek I. Regioselective carbon-carbon bond cleavage in the oxidation of cyclopropenylcarbinols. Organic Letters. 13: 4076-9. PMID 21732683 DOI: 10.1021/Ol201581C |
0.414 |
|
| 2011 |
Mejuch T, Botoshansky M, Marek I. Combined carbometalation-zinc homologation-allylation reactions as a new approach for alkoxyallylation of aldehydes. Organic Letters. 13: 3604-7. PMID 21675728 DOI: 10.1021/Ol201221D |
0.489 |
|
| 2011 |
Gilboa N, Wang H, Houk KN, Marek I. Axial preferences in allylations via the Zimmerman-Traxler transition state. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 8000-4. PMID 21647996 DOI: 10.1002/Chem.201101049 |
0.525 |
|
| 2011 |
Brebion F, Vincent G, Chelli S, Kwasnieski O, Najera F, Delouvrié B, Marek I, Derat E, Goddard JP, Malacria M, Fensterbank L. Conjugate additions to alkylidene bis(sulfoxides). Chemistry, An Asian Journal. 6: 1825-33. PMID 21400664 DOI: 10.1002/Asia.201000904 |
0.535 |
|
| 2011 |
Das JP, Marek I. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems. Chemical Communications (Cambridge, England). 47: 4593-623. PMID 21359322 DOI: 10.1039/C0Cc05222A |
0.481 |
|
| 2011 |
Ackermann L, Kozhushkov SI, Yufit DS, Marek I. Efficient Brønsted acid catalyzed hydrations and hydroaminations of (dicyclopropylmethylene)cyclopropane Synlett. 1515-1518. DOI: 10.1055/S-0030-1260769 |
0.4 |
|
| 2010 |
Basheer A, Marek I. Recent advances in carbocupration of α-heterosubstituted alkynes. Beilstein Journal of Organic Chemistry. 6. PMID 20703385 DOI: 10.3762/Bjoc.6.77 |
0.428 |
|
| 2010 |
Masarwa A, Marek I. Selectivity in metal-catalyzed carbon-carbon bond cleavage of alkylidenecyclopropanes. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9712-21. PMID 20607773 DOI: 10.1002/Chem.201001246 |
0.454 |
|
| 2010 |
Dutta B, Gilboa N, Marek I. Highly diastereoselective preparation of homoallylic alcohols containing two contiguous quaternary stereocenters in acyclic systems from simple terminal alkynes. Journal of the American Chemical Society. 132: 5588-9. PMID 20355731 DOI: 10.1021/Ja101371X |
0.399 |
|
| 2010 |
Simaan S, Marek I. Hydroformylation reaction of alkylidenecyclopropane derivatives: a new pathway for the formation of acyclic aldehydes containing quaternary stereogenic carbons. Journal of the American Chemical Society. 132: 4066-7. PMID 20205421 DOI: 10.1021/Ja100544C |
0.516 |
|
| 2010 |
Simaan S, Goldberg AF, Rosset S, Marek I. Metal-catalyzed ring-opening of alkylidenecyclopropanes: new access to building blocks with an acyclic quaternary stereogenic center. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 774-8. PMID 19950341 DOI: 10.1002/Chem.200902656 |
0.59 |
|
| 2010 |
Levin A, Basheer A, Marek I. Regiodivergent carbometalation reactions of ynol ether derivatives Synlett. 329-332. DOI: 10.1055/S-0029-1219221 |
0.465 |
|
| 2010 |
Ivanov R, Marek I, Cohen T. The superiority of properly prepared lithium 1-N,N-dimethylaminonaphthalenide (LDMAN) over other aromatic radical-anions for the generation of organolithiums by reductive lithiation Tetrahedron Letters. 51: 174-176. DOI: 10.1016/J.Tetlet.2009.10.121 |
0.305 |
|
| 2010 |
Unger R, Cohen T, Marek I. Diastero- and enantioselective intramolecular carbometalation reaction Tetrahedron. 66: 4874-4881. DOI: 10.1016/J.Tet.2010.04.038 |
0.467 |
|
| 2010 |
Marek I, Gandelmann M. Nobel-winning chemistry Israel Journal of Chemistry. 50: 541. DOI: 10.1002/Ijch.201000072 |
0.311 |
|
| 2010 |
Majumdar S, de Meijere A, Marek I. ChemInform Abstract: Catalytic Asymmetric and Stereoselective Synthesis of Vinylcyclopropanes. Cheminform. 33: no-no. DOI: 10.1002/chin.200230093 |
0.376 |
|
| 2010 |
Vu VA, Marek I, Polborn K, Knochel P. ChemInform Abstract: Preparation of New Functionalized Cyclopropylmagnesium Reagents. Cheminform. 33: no-no. DOI: 10.1002/chin.200230092 |
0.367 |
|
| 2010 |
Chakraborty A, Marek I. ChemInform Abstract: New One-Pot Synthesis of ω-Iodoalkyne. Cheminform. 31: no-no. DOI: 10.1002/chin.200034077 |
0.303 |
|
| 2010 |
Avolio S, Malan C, Marek I, Knochel P. ChemInform Abstract: Preparation and Reactions of Functionalized Magnesium Carbenoids. Cheminform. 31: no-no. DOI: 10.1002/chin.200006070 |
0.454 |
|
| 2010 |
Marek I. ChemInform Abstract: Enantioselective Carbometalation of Unactivated Olefins Cheminform. 30: no-no. DOI: 10.1002/chin.199930265 |
0.362 |
|
| 2010 |
BRASSEUR D, REZAEI H, FUXA A, ALEXAKIS A, MANGENEY P, MAREK I, NORMANT JF. ChemInform Abstract: First Diastereoselective Asymmetric Carbometallation of Chiral Vinyl Metals. Cheminform. 29: no-no. DOI: 10.1002/chin.199839021 |
0.491 |
|
| 2010 |
NORSIKIAN S, MAREK I, POISSON J, NORMANT JF. ChemInform Abstract: Enantioselective Carbolithiation of Cinnamyl Acetals. New Access to Chiral Disubstituted Cyclopropanes. Cheminform. 28: no-no. DOI: 10.1002/chin.199752037 |
0.334 |
|
| 2010 |
LORTHIOIS E, MAREK I, NORMANT J. ChemInform Abstract: Zinca-ene-allene Cyclizations: A Way to Substituted Tetrahydrofurans or Pyrrolidines. Cheminform. 28: no-no. DOI: 10.1002/chin.199746064 |
0.383 |
|
| 2010 |
LORTHIOIS E, MAREK I, NORMANT J. ChemInform Abstract: Zinca-ene-allene and Zinc-enolate Cyclization. Towards the Synthesis of Polysubstituted Pyrrolidines. Cheminform. 28: no-no. DOI: 10.1002/chin.199720113 |
0.716 |
|
| 2010 |
CRETON I, MAREK I, NORMANT J. ChemInform Abstract: Stereoselective Synthesis of Polysubstituted Olefins via the Formation of 1,1-Bimetalloalkenes. Cheminform. 27: no-no. DOI: 10.1002/chin.199604105 |
0.388 |
|
| 2010 |
MEYER C, MAREK I, COURTEMANCHE G, NORMANT J. ChemInform Abstract: Intramolecular Metallo-Ene-Allene Reactions. A New Carbocycles Synthesis. Cheminform. 26: no-no. DOI: 10.1002/chin.199532118 |
0.426 |
|
| 2010 |
LORTHIOIS E, MAREK I, MEYER C, NORMANT J. ChemInform Abstract: Zinca-en-allene Cyclization: Synthesis of Substituted Tetrahydrofurans. Cheminform. 26: no-no. DOI: 10.1002/chin.199526108 |
0.407 |
|
| 2010 |
MEYER C, MAREK I, COURTEMANCHE G, NORMANT J. ChemInform Abstract: Intramolecular Carbometallation of Organozinc Reagents. Cheminform. 26: no-no. DOI: 10.1002/chin.199512096 |
0.331 |
|
| 2010 |
MAREK I, ALEXAKIS A, NORMANT J. ChemInform Abstract: γ-Tributylstannyl β-Metallated Acrolein: A Versatile Synthon. Cheminform. 23: no-no. DOI: 10.1002/chin.199227229 |
0.405 |
|
| 2010 |
MAREK I, ALEXAKIS A, NORMANT J. ChemInform Abstract: A Highly Efficient Synthesis of Z-γ-Iodo Allylic Alcohols. Cheminform. 23: no-no. DOI: 10.1002/chin.199223106 |
0.484 |
|
| 2010 |
ALEXAKIS A, MAREK I, MANGENEY P, NORMANT JF. ChemInform Abstract: Diastereoselective Syn or Anti Opening of Propargylic Epoxides. Synthesis of α-Allenic Alcohols. Cheminform. 22: no-no. DOI: 10.1002/chin.199123061 |
0.48 |
|
| 2010 |
Simaan S, Goldberg AFG, Rosset S, Marek I. Metal-catalyzed ring-opening of alkylidenecyclopropanes: New access to building blocks with an acyclic quaternary stereogenic center Chemistry - a European Journal. 16: 774-778. DOI: 10.1002/chem.200902656 |
0.541 |
|
| 2009 |
Das JP, Chechik H, Marek I. A unique approach to aldol products for the creation of all-carbon quaternary stereocentres. Nature Chemistry. 1: 128-32. PMID 21378825 DOI: 10.1038/Nchem.131 |
0.464 |
|
| 2009 |
Marek I. Chemistry. The basics of zinc activation. Science (New York, N.Y.). 326: 673-4. PMID 19900920 DOI: 10.1126/Science.1181863 |
0.368 |
|
| 2009 |
Masarwa A, Fürstner A, Marek I. Metal-catalyzed rearrangement of enantiomerically pure alkylidenecyclopropane derivatives as a new access to cyclobutenes possessing quaternary stereocenters. Chemical Communications (Cambridge, England). 5760-2. PMID 19774261 DOI: 10.1039/B910465H |
0.383 |
|
| 2009 |
Simaan S, Masarwa A, Zohar E, Stanger A, Bertus P, Marek I. Cyclopropenylcarbinol derivatives as new versatile intermediates in organic synthesis: application to the formation of enantiomerically pure alkylidenecyclopropane derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 8449-64. PMID 19609999 DOI: 10.1002/Chem.200901074 |
0.551 |
|
| 2009 |
Unger R, Weisser F, Chinkov N, Stanger A, Cohen T, Marek I. Enantio- and diastereoselective tandem zn-promoted brook rearrangement/ene-allene carbocyclization reaction. Organic Letters. 11: 1853-6. PMID 19290654 DOI: 10.1021/Ol9004036 |
0.505 |
|
| 2009 |
Simaan S, Marek I. Copper-catalyzed hydride transfer from LiAlH(4) for the formation of alkylidenecyclopropane derivatives. Chemical Communications (Cambridge, England). 292-4. PMID 19209306 DOI: 10.1039/B817710D |
0.427 |
|
| 2009 |
Unger R, Cohen T, Marek I. Tandem Zn-Brook rearrangement/ene-allene carbocyclization European Journal of Organic Chemistry. 1749-1756. DOI: 10.1002/Ejoc.200900043 |
0.431 |
|
| 2009 |
Tsoglin E, Chechik H, Karseboom G, Chinkov N, Stanger A, Marek I. Stereoselective synthesis of metalated cyclobutyl derivatives Advanced Synthesis and Catalysis. 351: 1005-1008. DOI: 10.1002/Adsc.200800719 |
0.507 |
|
| 2008 |
Levin A, Marek I. Cyclopropenyllithiums as a new source of 1,1-bismetalated cyclopropyl derivatives. Chemical Communications (Cambridge, England). 4300-2. PMID 18802550 DOI: 10.1039/B807635A |
0.358 |
|
| 2008 |
Abramovitch A, Fensterbank L, Malacria M, Marek I. Convergent preparation of enantiomerically pure polyalkylated cyclopropane derivatives. Angewandte Chemie (International Ed. in English). 47: 6865-8. PMID 18661465 DOI: 10.1002/Anie.200802093 |
0.402 |
|
| 2008 |
Marek I. A shift in retrosynthetic paradigm. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 7460-8. PMID 18561353 DOI: 10.1002/Chem.200800580 |
0.431 |
|
| 2008 |
Füger B, Sklute G, Marek I, Bolm GY, Bolm C. Synthesis of sulfoximidoyl-substituted triazoles by huisgen 1,3-dipolar cycloaddition Synlett. 0116-0118. DOI: 10.1055/S-2007-1000837 |
0.496 |
|
| 2008 |
Abramovitch A, Marek I. Zinc homologation-elimination reaction of α-sulfinyl carbanions as a new route to olefins European Journal of Organic Chemistry. 4924-4931. DOI: 10.1002/Ejoc.200800529 |
0.389 |
|
| 2008 |
Kolodney G, Sklute G, Perrone S, Knochel P, Marek I. ChemInform Abstract: Diastereodivergent Synthesis of Enantiomerically Pure Homoallylic Amine Derivatives Containing Quaternary Carbon Stereocenters. Cheminform. 39. DOI: 10.1002/chin.200815071 |
0.493 |
|
| 2008 |
Marek I, Simaan S, Masarwa A. Enantiomerically enriched cyclopropene derivatives: Versatile building blocks in asymmetric synthesis (Angewandte Chemie - International Edition (2007) 46, (7364-7376) DOI: 10.1002/anie.200604774 Angewandte Chemie - International Edition. 47: 1982. DOI: 10.1002/anie.200890046 |
0.303 |
|
| 2007 |
Cohen T, Gibney H, Ivanov R, Yeh EA, Marek I, Curran DP. Intramolecular carbozincation of unactivated alkenes occurs through a zinc radical transfer mechanism. Journal of the American Chemical Society. 129: 15405-9. PMID 17988132 DOI: 10.1021/Ja076554K |
0.367 |
|
| 2007 |
Kolodney G, Sklute G, Perrone S, Knochel P, Marek I. Diastereodivergent synthesis of enantiomerically pure homoallylic amine derivatives containing quaternary carbon stereocenters. Angewandte Chemie (International Ed. in English). 46: 9291-4. PMID 17893895 DOI: 10.1002/Anie.200702981 |
0.557 |
|
| 2007 |
Masarwa A, Stanger A, Marek I. An efficient, facile, and general stereoselective synthesis of heterosubstituted alkylidenecyclopropanes. Angewandte Chemie (International Ed. in English). 46: 8039-42. PMID 17854109 DOI: 10.1002/Anie.200702713 |
0.403 |
|
| 2007 |
Marek I, Simaan S, Masarwa A. Enantiomerically enriched cyclopropene derivatives: versatile building blocks in asymmetric synthesis. Angewandte Chemie (International Ed. in English). 46: 7364-76. PMID 17663496 DOI: 10.1002/Anie.200604774 |
0.447 |
|
| 2007 |
Simaan S, Marek I. Stereodivergent carbometalation reactions of cyclopropenylcarbinol derivatives. Organic Letters. 9: 2569-71. PMID 17536813 DOI: 10.1021/Ol070974X |
0.464 |
|
| 2007 |
Marek I, Sklute G. Creation of quaternary stereocenters in carbonyl allylation reactions. Chemical Communications (Cambridge, England). 1683-91. PMID 17457409 DOI: 10.1039/B615042J |
0.446 |
|
| 2007 |
Sklute G, Bolm C, Marek I. Regio- and stereoselective copper-catalyzed carbozincation reactions of alkynyl sulfoximines and sulfones. Organic Letters. 9: 1259-61. PMID 17348664 DOI: 10.1021/Ol070070B |
0.513 |
|
| 2006 |
Simaan S, Masarwa A, Bertus P, Marek I. Enantiomerically pure cyclopropenylcarbinols as a source of chiral alkylidenecyclopropane derivatives. Angewandte Chemie (International Ed. in English). 45: 3963-5. PMID 16625668 DOI: 10.1002/Anie.200600556 |
0.43 |
|
| 2006 |
Sklute G, Marek I. New multicomponent approach for the creation of chiral quaternary centers in the carbonyl allylation reactions. Journal of the American Chemical Society. 128: 4642-9. PMID 16594701 DOI: 10.1021/Ja060498Q |
0.468 |
|
| 2006 |
Marek I, Chinkov N, Levin A. A zirconium promenade - An efficient tool in organic synthesis Synlett. 501-514. DOI: 10.1055/S-2006-932483 |
0.524 |
|
| 2005 |
Unger R, Cohen T, Marek I. New tandem Zn-promoted Brook rearrangement/ene-allene carbocyclization reactions. Organic Letters. 7: 5313-6. PMID 16268566 DOI: 10.1021/Ol052237B |
0.483 |
|
| 2005 |
Kopp F, Sklute G, Polborn K, Marek I, Knochel P. Stereoselective functionalization of cyclopropane derivatives using bromine/magnesium and sulfoxide/magnesium exchange reactions. Organic Letters. 7: 3789-91. PMID 16092876 DOI: 10.1021/Ol051452P |
0.501 |
|
| 2005 |
Chechik-Lankin H, Marek I. Preparation and synthetic transformation of alkenyl carbamates into vinyl zirconocene derivatives Synthesis. 3311-3318. DOI: 10.1055/S-2005-918436 |
0.482 |
|
| 2005 |
Zohar E, Stanger A, Marek I. Synthesis of chiral methylenecyclopropane derivatives Synlett. 2239-2241. DOI: 10.1055/S-2005-872247 |
0.492 |
|
| 2005 |
Chechik-Lankin H, Livshin S, Marek I. Regiocontrolled carbometallation reactions of ynamides Synlett. 2098-2100. DOI: 10.1055/S-2005-871962 |
0.484 |
|
| 2005 |
Kopp F, Sklute G, Polborn K, Marek I, Knochel P. Stereoselective Functionalization of Cyclopropane Derivatives Using Bromine/Magnesium and Sulfoxide/Magnesium Exchange Reactions. Cheminform. 36. DOI: 10.1002/chin.200552054 |
0.468 |
|
| 2005 |
Leroux F, Schlosser M, Zohar E, Marek I. The Preparation of Organolithium Reagents and Intermediates Cheminform. 36. DOI: 10.1002/9780470682531.Pat0305 |
0.384 |
|
| 2004 |
Abramovitch A, Varghese JP, Marek I. Alpha-sulfinyl carbanions as a new source of olefins. Organic Letters. 6: 621-3. PMID 14961638 DOI: 10.1021/Ol036450O |
0.306 |
|
| 2004 |
Zohar E, Marek I. Diastereoselective reduction of cyclopropenylcarbinol: new access to anti-cyclopropylcarbinol derivatives. Organic Letters. 6: 341-3. PMID 14748588 DOI: 10.1021/Ol036143I |
0.443 |
|
| 2004 |
Chinkov N, Sklute G, Chechik H, Abramovitch A, Amsallem D, Varghese J, Majumdar S, Marek I. New regio-, stereo-, diastereo-, and enantioselective one-pot reactions mediated by organometallic derivatives Pure and Applied Chemistry. 76: 517-535. DOI: 10.1351/Pac200476030517 |
0.572 |
|
| 2004 |
Chinkov N, Majumdar S, Marek I. Stereoselective synthesis and reactivity of dienyl zirconocene derivatives Synthesis. 2411-2417. DOI: 10.1055/S-2004-829189 |
0.538 |
|
| 2004 |
Zohar E, Ram M, Marek I. Stereoselective preparation of deuteriated dienes by ring fragmentation of metallated cyclopropylcarbinols Synlett. 1288-1290. DOI: 10.1055/S-2004-822918 |
0.534 |
|
| 2004 |
Vu VA, Marek I, Knochel P. Stereoselective Preparation of Functionalized Unsaturated Lactones and Esters via Functionalized Magnesium Carbenoids. Cheminform. 35. DOI: 10.1055/S-2003-41035 |
0.538 |
|
| 2004 |
Farhat S, Zouev I, Marek I. From vinyl sulfides, sulfoxides and sulfones to vinyl zirconocene derivatives Tetrahedron. 60: 1329-1337. DOI: 10.1016/J.Tet.2003.08.074 |
0.475 |
|
| 2004 |
Wiedemann S, Rauch K, Savchenko A, Marek I, De Meijere A. Convenient Route to 2-(Trialkylstannyl)cyclopropylamines and Their Application in Palladium-Catalyzed Cross-Coupling Reactions European Journal of Organic Chemistry. 631-635. DOI: 10.1002/Ejoc.200300454 |
0.479 |
|
| 2004 |
Wiedemann S, Rauch K, Savchenko A, Marek I, de Meijere A. Cyclopropyl Building Blocks for Organic Synthesis. Part 97. Convenient Route to 2-(Trialkylstannyl)cyclopropylamines and Their Application in Palladium-Catalyzed Cross-Coupling Reactions. Cheminform. 35. DOI: 10.1002/chin.200422090 |
0.329 |
|
| 2003 |
Chechik-Lankin H, Marek I. Regio- and stereoselective synthesis of novel (E)-1-alkenyl carbamate via carbocupration reaction. Organic Letters. 5: 5087-9. PMID 14682771 DOI: 10.1021/Ol036154B |
0.497 |
|
| 2003 |
Chinkov N, Majumdar S, Marek I. Stereoselective preparation of dienyl zirconocene complexes via a tandem allylic C-H bond activation-elimination sequence. Journal of the American Chemical Society. 125: 13258-64. PMID 14570502 DOI: 10.1021/Ja036751T |
0.399 |
|
| 2003 |
Sklute G, Amsallem D, Shabli A, Varghese JP, Marek I. Four-component reactions for a new diastereoselective synthesis of chiral quaternary centers. Journal of the American Chemical Society. 125: 11776-7. PMID 14505373 DOI: 10.1021/Ja036872T |
0.55 |
|
| 2003 |
Chinkov N, Chechik H, Majumdar S, Liard A, Marek I. New Preparation of sp2 Organometallic Derivatives Cheminform. 34. DOI: 10.1055/S-2002-35622 |
0.438 |
|
| 2003 |
Marek I. Sp3 Organozinc Carbenoid Homologation in Organic Synthesis. Cheminform. 34. DOI: 10.1016/S0040-4020(02)01186-9 |
0.331 |
|
| 2003 |
Vu VA, Marek I, Knochel P. Stereoselective preparation of functionalized unsaturated lactones and esters via functionalized magnesium carbenoids Synthesis. 1797-1802. |
0.361 |
|
| 2003 |
Marek I. Synthesis and reactivity of geminated organobismetallic derivatives Actualite Chimique. 17-24. |
0.344 |
|
| 2002 |
Vu VA, Marek I, Polborn K, Knochel P. Preparation of new functionalized cyclopropylmagnesium reagents. Angewandte Chemie (International Ed. in English). 41: 351-2. PMID 12491430 DOI: 10.1002/1521-3773(20020118)41:2<351::Aid-Anie351>3.0.Co;2-5 |
0.445 |
|
| 2002 |
Chinkov N, Majumdar S, Marek I. New approach to the stereoselective synthesis of metalated dienes via an isomerization-elimination sequence. Journal of the American Chemical Society. 124: 10282-3. PMID 12197722 DOI: 10.1021/Ja027027Y |
0.445 |
|
| 2002 |
Hupe E, Marek I, Knochel P. Diastereoselective reduction of alkenylboronic esters as a new method for controlling the stereochemistry of up to three adjacent centers in cyclic and acyclic molecules. Organic Letters. 4: 2861-3. PMID 12182574 DOI: 10.1021/Ol0262486 |
0.525 |
|
| 2002 |
Majumdar S, de Meijere A, Marek I. Catalytic Asymmetric and Stereoselective Synthesis of Vinylcyclopropanes Synlett. 2002: 0423-0426. DOI: 10.1055/S-2002-20456 |
0.501 |
|
| 2002 |
Chinkov N, Morlender-Vais N, Marek I. New preparation of stereodefined α, α-unsaturated ketones by carbomagnesiation of α-allenyl ketones Tetrahedron Letters. 43: 6009-6010. DOI: 10.1016/S0040-4039(02)01211-X |
0.377 |
|
| 2002 |
Vu VA, Marek I, Polborn K, Knochel P. Preparation of New Functionalized Cyclopropylmagnesium Reagents Angewandte Chemie. 114: 361-362. DOI: 10.1002/1521-3757(20020118)114:2<361::aid-ange361>3.0.co;2-q |
0.346 |
|
| 2002 |
Varghese JP, Zouev I, Aufauvre L, Knochel P, Marek I. Carbocupration/Zinc Carbenoid Homologation and β‐Elimination Reactions for a New Synthesis of Allenes − Application to the Enantioselective Synthesis of Chiral Allenes by Deracemization of sp3‐Organometallic Derivatives European Journal of Organic Chemistry. 2002: 4151-4158. DOI: 10.1002/1099-0690(200212)2002:24<4151::Aid-Ejoc4151>3.0.Co;2-S |
0.61 |
|
| 2002 |
Chinkov N, Chechik H, Majumdar S, Marek I, Liard A. New preparation of sp2 organometallic derivatives Synthesis. 2473-2483. |
0.394 |
|
| 2002 |
Varghese JP, Zouev I, Aufauvre L, Knochel P, Marek I. Carbocupration/zinc carbenoid homologation and β-elimination reactions for a new synthesis of allenes - Application to the enantioselective synthesis of chiral allenes by deracemization of sp3-organometallic derivatives European Journal of Organic Chemistry. 4151-4158. |
0.455 |
|
| 2001 |
Shibli A, Varghese JP, Knochel P, Marek I. Improved Preparation of Secondary Zinc Iodides by 1,2-Migration of sp3 Carbenoids Synlett. 2001: 818-820. DOI: 10.1055/S-2001-14602 |
0.428 |
|
| 2001 |
Rezaei H, Marek I, Normant JF. Diastereoselective carbozincation of propargylic amines Tetrahedron. 57: 2477-2483. DOI: 10.1016/S0040-4020(01)00069-2 |
0.707 |
|
| 2001 |
Liard A, Kaftanov J, Chechik H, Farhat S, Morlender-Vais N, Averbuj C, Marek I. Addition–β-elimination: a new method for the preparation of organometallic compounds Journal of Organometallic Chemistry. 624: 26-33. DOI: 10.1016/S0022-328X(00)00842-1 |
0.429 |
|
| 2001 |
Marek I. Foreword by the Guest Editors: Asymmetric Synthesis Israel Journal of Chemistry. 41: NA-NA. DOI: 10.1002/Ijch.5680410401 |
0.444 |
|
| 2000 |
Liard A, Marek I. Stereoselective preparation of E vinyl zirconium derivatives from E or Z enol ethers Journal of Organic Chemistry. 65: 7218-7220. PMID 11031055 DOI: 10.1021/Jo005561N |
0.31 |
|
| 2000 |
Varghese JP, Knochel P, Marek I. New allene synthesis via carbocupration-zinc carbenoid homologation and beta-elimination sequence. Organic Letters. 2: 2849-52. PMID 10964381 DOI: 10.1021/Ol006276T |
0.521 |
|
| 2000 |
Chakraborty A, Marek I. New One-Pot Synthesis of ò-Iodoalkyne Synthetic Communications. 30: 1895-1901. DOI: 10.1080/00397910008087238 |
0.4 |
|
| 2000 |
Morlender-Vais N, Kaftanov J, Marek I. Synthesis and Reactivity of Functionalized Alkynyl Titanium Derivatives Synthesis. 2000: 917-920. DOI: 10.1055/S-2000-6288 |
0.426 |
|
| 2000 |
Morlender-Vais N, Solodovnikova N, Marek I. Intramolecular carbometalation of functionalized terminal alkynes via low-valent titanium complexes Chemical Communications. 1849-1850. DOI: 10.1039/B005027J |
0.394 |
|
| 2000 |
Kaftanov J, Averbuj C, Vais-Morlender N, Liard A, Marek I. Synthesis and reactivity of polymetallated olefins and functionalized metalloalkynes Polyhedron. 19: 563-566. DOI: 10.1016/S0277-5387(99)00408-8 |
0.395 |
|
| 2000 |
Morlender-Vais N, Kaftanov J, Marek I. ChemInform Abstract: Synthesis and Reactivity of Functionalized Alkynyl Titanium Derivatives. Cheminform. 31: no-no. DOI: 10.1002/chin.200039060 |
0.334 |
|
| 1999 |
Averbuj C, Kaftanov J, Marek I. First Synthesis of Metallated Titanacyclopropenes Synlett. 1999: 1939-1941. DOI: 10.1055/S-1999-2964 |
0.327 |
|
| 1999 |
Avolio S, Malan C, Marek I, Knochel P. Preparation and Reactions of Functionalized Magnesium Carbenoids Synlett. 1999: 1820-1822. DOI: 10.1055/S-1999-2935 |
0.516 |
|
| 1999 |
Aufauvre L, Marek I, Knochel P. A new approach towards the synthesis of sp3 1,1-diiodoalkanes Chemical Communications. 2207-2208. DOI: 10.1039/A907355H |
0.476 |
|
| 1999 |
Chakraborty A, Marek I. Iodine transfer cyclization mediated by DIBAL-H/THF Chemical Communications. 2375-2376. DOI: 10.1039/A906952F |
0.34 |
|
| 1999 |
Marek I, Schreiner PR, Normant JF. Allyl zincation of vinyl metals: A computational study Organic Letters. 1: 929-931. DOI: 10.1021/Ol990843Z |
0.683 |
|
| 1999 |
Bremand N, Marek I, Normant JF. Diastereoselective 'contra-Michael' addition of (-)- sparteine/organolithium complexes to secondary chiral cinnamyl amides Tetrahedron Letters. 40: 3383-3386. DOI: 10.1016/S0040-4039(99)00495-5 |
0.681 |
|
| 1999 |
Bremand N, Marek I, Normant JF. Regioselective addition of nbutyllithium on secondary cinnamyl amides: 'Michael' versus 'contra-Michael' process Tetrahedron Letters. 40: 3379-3382. DOI: 10.1016/S0040-4039(99)00494-3 |
0.646 |
|
| 1999 |
Creton I, Rezaei H, Marek I, Normant JF. First transfer of chirality in the Fritsch-Buttenberg-Wiechell rearrangement, via zinc carbenoids: A migration with retention of configuration Tetrahedron Letters. 40: 1899-1902. DOI: 10.1016/S0040-4039(99)00090-8 |
0.696 |
|
| 1999 |
Norsikian S, Marek I, Klein S, Poisson JF, Normant JF. Enantioselective carbometalation of cinnamyl derivatives: New access to chiral disubstituted cyclopropanes - Configurational stability of benzylic organozinc halides Chemistry - a European Journal. 5: 2055-2068. DOI: 10.1002/(Sici)1521-3765(19990702)5:7<2055::Aid-Chem2055>3.0.Co;2-9 |
0.72 |
|
| 1998 |
Brasseur D, Marek I, Normant JF. Diastereoselective carbometalation of chiral vinyl metals Comptes Rendus De L'Academie Des Sciences - Series Iic: Chemistry. 1: 621-625. DOI: 10.1016/S1387-1609(99)80017-6 |
0.696 |
|
| 1998 |
Brasseur D, Rezaei H, Fuxa A, Alexakis A, Mangeney P, Marek I, Normant JF. First diastereoselective asymmetric carbometallation of chiral vinyl metals Tetrahedron Letters. 39: 4821-4824. DOI: 10.1016/S0040-4039(98)00942-3 |
0.761 |
|
| 1998 |
Folléas B, Marek I, Normant J, Jalmes LS. Fluoroform: an efficient precursor for the trifluoromethylation of aldehydes Tetrahedron Letters. 39: 275-283. DOI: 10.1016/S0040-4020(99)00951-5 |
0.374 |
|
| 1997 |
Norsikian S, Marek I, Poisson JF, Normant JF. Enantioselective carbolithiation of cinnamyl acetals. New access to chiral disubstituted cyclopropanes Journal of Organic Chemistry. 62: 4898-4899. DOI: 10.1021/Jo9705172 |
0.708 |
|
| 1997 |
Norsikian S, Marek I, Normant JF. Enantioselective carbolithiation of β-alkylated styrene Tetrahedron Letters. 38: 7523-7526. DOI: 10.1016/S0040-4039(97)10022-3 |
0.665 |
|
| 1997 |
Lorthiois E, Marek I, Normant J. Zinca-ene-allene and zinc-enolate cyclization. Towards the synthesis of polysubstituted pyrrolidines Tetrahedron Letters. 38: 89-92. DOI: 10.1016/S0040-4039(96)02222-8 |
0.752 |
|
| 1996 |
Marek I, Normant JF. Synthesis and Reactivity of sp(3)-Geminated Organodimetallics. Chemical Reviews. 96: 3241-3268. PMID 11848859 DOI: 10.1021/Cr9600161 |
0.678 |
|
| 1996 |
Creton I, Marek I, Normant JF. Synthesis of polysubstituted stereodefined olefins via the reactivity of sp2 organo-gem-bismetallics Synthesis. 1499-1508. DOI: 10.1055/S-1996-4422 |
0.691 |
|
| 1996 |
Lorthiois E, Marek I, Meyer C, Normant JF. Intermolecular carbolithiation of silylated enynes Tetrahedron Letters. 37: 6689-6692. DOI: 10.1016/S0040-4039(96)01447-5 |
0.796 |
|
| 1996 |
Lorthiois E, Marek I, Normant JF. Intramolecular carbolithiation of silylated enynes Tetrahedron Letters. 37: 6693-6694. DOI: 10.1016/S0040-4039(96)01447-5 |
0.718 |
|
| 1996 |
Marek I, Normant JF. Synthesis and reactivity of sp3-geminated organodimetallics Chemical Reviews. 96: 3241-3267. |
0.651 |
|
| 1995 |
Meyer C, Marek I, Courtemanche G, Normant J. Intramolecular Metallo-Ene-Allene Reactions. A New Carbocycles Synthesis The Journal of Organic Chemistry. 60: 863-871. DOI: 10.1021/Jo00109A017 |
0.51 |
|
| 1995 |
Klein S, Marek I, Poisson JF, Normant JF. Asymmetric carbolithiation of cinnamyl derivatives in the presence of (-)-sparteine Journal of the American Chemical Society. 117: 8853-8854. DOI: 10.1021/Ja00139A020 |
0.694 |
|
| 1995 |
Creton I, Marek I, Normant JF. Stereoselective synthesis of polysubstituted olefins via the formation of 1,1-bimetalloalkenes Tetrahedron Letters. 36: 7451-7454. DOI: 10.1016/0040-4039(95)01551-5 |
0.766 |
|
| 1995 |
Marek I, Beruben D, Normant JF. Metal-alkene π-chelation: A stereodirecting effect in allylzincation reactions and in zinc mediated cyclopropanations Tetrahedron Letters. 36: 3695-3698. DOI: 10.1016/0040-4039(95)00614-I |
0.715 |
|
| 1995 |
Lorthiois E, Marek I, Meyer C, Normant JF. Zinca-en-allene cyclization synthesis of substituted tetrahydrofurans Tetrahedron Letters. 36: 1263-1266. DOI: 10.1016/0040-4039(94)02483-R |
0.839 |
|
| 1994 |
Klein S, Marek I, Normant JF. Carbolithiation of cinnamyldialkylamines. Stereochemistry of the Li to Zn transmetalation and configurational stability of benzylic organozinc halides Journal of Organic Chemistry. 59: 2925-2926. DOI: 10.1021/Jo00090A005 |
0.678 |
|
| 1994 |
Meyer C, Marek I, Courtemanche G, Normant JF. Intramolecular carbometallation of organozinc reagents. Tetrahedron. 50: 11665-11692. DOI: 10.1016/S0040-4020(01)85661-1 |
0.83 |
|
| 1994 |
Creton I, Marek I, Brasseur D, Jestin JL, Normant JF. Phenylthioacetylene as a source of stereodefined trisubstituted alkenes Tetrahedron Letters. 35: 6873-6876. DOI: 10.1016/0040-4039(94)85028-3 |
0.675 |
|
| 1993 |
Meyer C, Marek I, Normant J. (E)- or (Z)-β-Iodoacrolein. A Novel Versatile Synthon Synlett. 1993: 386-388. DOI: 10.1055/S-1993-22463 |
0.613 |
|
| 1993 |
Meyer C, Marek I, Courtemanche G, Normant J. Carbocyclization of Functionalized Zinc Organometallics Synlett. 1993: 266-268. DOI: 10.1055/S-1993-22426 |
0.631 |
|
| 1992 |
Marek I, Lefrançois JM, Normant JF. Iodocyclization of olefinic t-butyl ethers : an easy stereocontrolled synthesis of cis-substituted tetrahydrofurans. Tetrahedron Letters. 33: 1747-1748. DOI: 10.1016/S0040-4039(00)91722-2 |
0.672 |
|
| 1991 |
Marek I, Alexakis A, Normant JF. A highly efficient synthesis of (Z) γ-iodo allylic alcohols Tetrahedron Letters. 32: 5329-5332. DOI: 10.1016/S0040-4039(00)92377-3 |
0.757 |
|
| 1991 |
Alexakis A, Marek I, Mangeney P, Normant JF. Diastereoselective syn or anti opening of propargylic epoxides. Synthesis of α-allenic alcohols Tetrahedron. 47: 1677-1696. DOI: 10.1016/S0040-4020(01)96911-X |
0.759 |
|
| 1991 |
Marek I, Alexakis A, Normant JF. γ-Tributylstannyl-β-metallated acrolein : a versatile synthon Tetrahedron Letters. 32: 6337-6340. DOI: 10.1016/0040-4039(91)80163-Z |
0.71 |
|
| 1990 |
Alexakis A, Marek I, Mangeney P, Normant JF. Mechanistic aspects of the formation of chiral allenes from propargylic ethers and organocopper reagents Journal of the American Chemical Society. 112: 8042-8047. DOI: 10.1021/ja00178a029 |
0.563 |
|
| 1990 |
Alexakis A, Marek I, Mangeney P, Normant JF. Mechanistic aspects on the formation of chiral allenes from propargylic ethers and organocopper reagents Journal of the American Chemical Society. 112: 8042-8047. DOI: 10.1021/Ja00178A029 |
0.769 |
|
| 1989 |
Alexakis A, Marek I, Mangeney P, Normant JF. Diastereoselective synthesis of α-allenic alcohols from propargylic epoxides Tetrahedron Letters. 30: 2387-2390. DOI: 10.1016/S0040-4039(01)80406-8 |
0.754 |
|
| 1989 |
ALEXAKIS A, MAREK I, MANGENEY P, NORMANT JF. ChemInform Abstract: Diastereoselective Synthesis of α-Allenic Alcohols from Propargylic Epoxides. Cheminform. 20. DOI: 10.1002/chin.198950071 |
0.479 |
|
| 1988 |
Alexakis A, Mangeney P, Ghribi A, Marek I, Sedrani R, Guir C, Normant J. Chiral acetals in enantio- and diastereoselective substitution or elimination reactions Pure and Applied Chemistry. 60: 49-56. DOI: 10.1351/Pac198860010049 |
0.639 |
|
| 1988 |
ALEXAKIS A, MANGENEY P, GHRIBI A, MAREK I, SEDRANI R, GUIR C, NORMANT J. ChemInform Abstract: Chiral Acetals in Enantio- and Diastereoselective Substitution or Elimination Reactions Cheminform. 19. DOI: 10.1002/chin.198828334 |
0.623 |
|
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