Ilan Marek - Publications

Affiliations: 
Chemistry Technion - Israel Institute of Technology, Haifa, Haifa District, Israel 

115 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Lanke V, Marek I. Nucleophilic Substitution at Quaternary Carbon Stereocenters. Journal of the American Chemical Society. PMID 32141750 DOI: 10.1021/jacs.0c01133  1
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  1
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  1
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  1
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  0.52
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  0.44
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  1
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  0.52
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  0.84
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  0.84
2016 Vasseur A, Bruffaerts J, Marek I. Remote functionalization through alkene isomerization. Nature Chemistry. 8: 209-19. PMID 26892551 DOI: 10.1038/nchem.2445  0.84
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  0.84
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  0.84
2016 Müller DS, Marek I. Copper mediated carbometalation reactions Chemical Society Reviews. 45: 4552-4566. DOI: 10.1039/c5cs00897b  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2015 Schwarz H, Willner I, Marek I. The Scientific Bridge: Fifty Years of Germany-Israel Diplomatic Relations. Angewandte Chemie (International Ed. in English). 54: 12182-3. PMID 26332020 DOI: 10.1002/anie.201506694  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2015 Vasseur A, Perrin L, Eisenstein O, Marek I. Remote functionalization of hydrocarbons with reversibility enhanced stereocontrol Chemical Science. 6: 2770-2776. DOI: 10.1039/c5sc00445d  0.84
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  0.84
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  0.84
2015 Vabre R, Island B, Diehl CJ, Schreiner PR, Marek I. Forming Stereogenic Centers in Acyclic Systems from Alkynes Angewandte Chemie - International Edition. DOI: 10.1002/anie.201504756  0.84
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  0.84
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  0.84
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  0.84
2014 Marek I. Chemistry in Israel--at a crossroads? Angewandte Chemie (International Ed. in English). 53: 3754-5. PMID 24677677 DOI: 10.1002/anie.201401092  0.84
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  0.84
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  0.84
2014 Minko Y, Marek I. Oxenoids in organic synthesis. Organic & Biomolecular Chemistry. 12: 1535-46. PMID 24477293 DOI: 10.1039/c3ob42349b  0.84
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  0.84
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  0.84
2014 Minko Y, Marek I. Advances in Carbolithiation Lithium Compounds in Organic Synthesis: From Fundamentals to Applications. 329-350. DOI: 10.1002/9783527667512.ch11  0.84
2014 Didier D, Marek I. Carbometallation Reactions Copper-Catalyzed Asymmetric Synthesis. 267-282. DOI: 10.1002/9783527664573.ch10  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2013 Marek I. Carbometallation chemistry. Beilstein Journal of Organic Chemistry. 9: 234-5. PMID 23399965 DOI: 10.3762/bjoc.9.27  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.4
2010 Levin A, Basheer A, Marek I. Regiodivergent carbometalation reactions of ynol ether derivatives Synlett. 329-332. DOI: 10.1055/s-0029-1219221  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2009 Marek I. Chemistry. The basics of zinc activation. Science (New York, N.Y.). 326: 673-4. PMID 19900920 DOI: 10.1126/science.1181863  0.84
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  0.84
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  0.84
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  0.84
2009 Unger R, Cohen T, Marek I. Tandem Zn-Brook rearrangement/ene-allene carbocyclization European Journal of Organic Chemistry. 1749-1756. DOI: 10.1002/ejoc200900043  0.84
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  0.84
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  0.84
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  0.84
2008 Marek I. A shift in retrosynthetic paradigm. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 7460-8. PMID 18561353 DOI: 10.1002/chem.200800580  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2007 Simaan S, Marek I. Stereodivergent carbometalation reactions of cyclopropenylcarbinol derivatives. Organic Letters. 9: 2569-71. PMID 17536813 DOI: 10.1021/ol070974x  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2006 Chinkov N, Levin A, Marek I. Unsaturated fatty alcohol derivatives as a source of substituted allylzirconocene. Angewandte Chemie (International Ed. in English). 45: 465-8. PMID 16342305 DOI: 10.1002/anie.200501946  0.84
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  0.84
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  0.84
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  0.84
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  0.84
2005 Zohar E, Stanger A, Marek I. Synthesis of chiral methylenecyclopropane derivatives Synlett. 2239-2241. DOI: 10.1055/s-2005-872247  0.84
2005 Chechik-Lankin H, Livshin S, Marek I. Regiocontrolled carbometallation reactions of ynamides Synlett. 2098-2100. DOI: 10.1055/s-2005-871962  0.84
2005 Marek I. Multicomponent reactions Tetrahedron. 61: 11309. DOI: 10.1016/j.tet.2005.09.041  0.84
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  0.84
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  0.84
2004 Chinkov N, Majumdar S, Marek I. Stereoselective synthesis and reactivity of dienyl zirconocene derivatives Synthesis. 2411-2417. DOI: 10.1055/s-2004-829189  0.84
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  0.84
2004 Zohar E, Ram M, Marek I. Stereoselective preparation of deuteriated dienes by ring fragmentation of metallated cyclopropylcarbinols Synlett. 1288-1290.  0.84
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.  0.84
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.  0.84
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  0.84
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  0.84
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  0.84
2003 Motiei L, Marek I, Gottlieb HE, Marks V, Lellouche JP. C-C bond formation using allylic organozirconium compounds. Nucleophilic additions on to isolated and in situ generated η5-pentadienyl-Fe(CO)3/Fe(CO)2PPh 3(+1) cations Tetrahedron Letters. 44: 5909-5912. DOI: 10.1016/S0040-4039(03)01363-7  0.84
2003 Vu VA, Marek I, Knochel P. Stereoselective preparation of functionalized unsaturated lactones and esters via functionalized magnesium carbenoids Synthesis. 1797-1802.  0.84
2003 Marek I. Synthesis and reactivity of geminated organobismetallic derivatives Actualite Chimique. 17-24.  0.84
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  0.84
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  0.84
2002 Marek I. Sp3 organozinc carbenoid homologation in organic synthesis Tetrahedron. 58: 9463-9475. DOI: 10.1016/S0040-4020(02)01186-9  0.84
2002 Chinkov N, Chechik H, Majumdar S, Marek I, Liard A. New preparation of sp2 organometallic derivatives Synthesis. 2473-2483.  0.84
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.  0.84
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