Year |
Citation |
Score |
2022 |
Abegg T, Cossy J, Meyer C. Cascade Cope/Winstein Rearrangements: Synthesis of Azido-Cycloheptadienes from Dialkenylcyclopropanes Possessing a Vinyl Azide. Organic Letters. PMID 35787030 DOI: 10.1021/acs.orglett.2c01888 |
0.577 |
|
2021 |
Lefebvre G, Charron O, Cossy J, Meyer C. Radical Addition of SFCl to Cyclopropenes: Synthesis of (Pentafluorosulfanyl)cyclopropanes. Organic Letters. PMID 34170712 DOI: 10.1021/acs.orglett.1c01840 |
0.475 |
|
2020 |
Meyer C, Yamani K, Pierre H, Archambeau A, Cossy J. Asymmetric transfer hydrogenation of gem-difluoro-cyclopropenyl esters. Access to enantio-enriched gem-difluorocyclopropanes. Angewandte Chemie (International Ed. in English). PMID 32614985 DOI: 10.1002/Anie.202008572 |
0.55 |
|
2019 |
Saiegh TJ, Chédotal H, Meyer C, Cossy J. Rhodium(III)-Catalyzed C(sp)-H Functionalization of Cyclobutenes. Access to Cyclobuta[]pyridones and -pyridines. Organic Letters. PMID 31584826 DOI: 10.1021/Acs.Orglett.9B03139 |
0.641 |
|
2019 |
Dupas A, Lhotellier PA, Guillamot G, Meyer C, Cossy J. Synthesis of Highly Substituted Azepanones from 2 H-Azirines by a Stepwise Annulation/Ring-Opening Sequence. Organic Letters. PMID 31026165 DOI: 10.1021/Acs.Orglett.9B00999 |
0.612 |
|
2019 |
Ernouf G, Brayer JL, Meyer C, Cossy J. Sigmatropic rearrangements of cyclopropenylcarbinol derivatives. Access to diversely substituted alkylidenecyclopropanes. Beilstein Journal of Organic Chemistry. 15: 333-350. PMID 30800182 DOI: 10.3762/Bjoc.15.29 |
0.553 |
|
2019 |
Lecourt C, Dhambri S, Yamani K, Boissonnat G, Specklin S, Fleury E, Hammad K, Auclair E, Sable S, Grondin A, Arimondo PB, Sautel F, Massiot G, Meyer C, Cossy J, et al. Assembly of the Entire Carbon Backbone of a Stereoisomer of the Antitumor Marine Natural Product Hemicalide. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30600846 DOI: 10.1002/Chem.201806327 |
0.473 |
|
2018 |
Ernouf G, Brayer JL, Folleas B, Demoute JP, Meyer C, Cossy J. [3,3]-Sigmatropic Rearrangement of Cyclopropenylcarbinyl Cyanates. Access to Alkylidene(aminocyclopropane) Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30021051 DOI: 10.1002/Chem.201803231 |
0.537 |
|
2017 |
Krieger JP, Lesuisse D, Ricci G, Perrin MA, Meyer C, Cossy J. Rhodium(III)-Catalyzed C-H Activation/Heterocyclization as a Macrocyclization Strategy. Synthesis of Macrocyclic Pyridones. Organic Letters. PMID 28485944 DOI: 10.1021/Acs.Orglett.7B01051 |
0.527 |
|
2017 |
Ernouf G, Brayer JL, Folleas B, Demoute JP, Meyer C, Cossy J. Synthesis of Alkylidene(gem-Difluorocyclopropanes) from Propargyl Glycolates by a One-Pot Difluorocyclopropenation/Ireland-Claisen Rearrangement Sequence. The Journal of Organic Chemistry. PMID 28277662 DOI: 10.1021/Acs.Joc.7B00197 |
0.526 |
|
2016 |
Lecourt C, Boinapally S, Dhambri S, Boissonnat G, Meyer C, Cossy J, Sautel F, Massiot G, Ardisson J, Sorin G, Lannou MI. Elaboration of Sterically Hindered δ-Lactones through Ring-Closing Metathesis: Application to the Synthesis of the C1-C27 Fragment of Hemicalide. The Journal of Organic Chemistry. 81: 12275-12290. PMID 27978725 DOI: 10.1021/Acs.Joc.6B02208 |
0.592 |
|
2016 |
Krieger JP, Ricci G, Lesuisse D, Cossy J, Meyer C. Harnessing C-H Activation of Benzhydroxamates as a Macrocyclization Strategy: Synthesis of Structurally Diverse Macrocyclic Isoquinolones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27219876 DOI: 10.1002/Chem.201602332 |
0.562 |
|
2016 |
Archambeau A, Nguyen DV, Meyer C, Cossy J. Rhodium(II)-Catalyzed Isomerization of Cyclopropenylmethyl Esters into (Acyloxymethylene)cyclopropanes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26990014 DOI: 10.1002/Chem.201505063 |
0.544 |
|
2016 |
Hiault F, Archambeau A, Miege F, Meyer C, Cossy J. Gold-Catalyzed Rearrangement of (Silylcyclopropenyl)methyl Ethers into (Silylmethylene)cyclopropanes Synthesis. 48: 3165-3174. DOI: 10.1055/S-0035-1561486 |
0.545 |
|
2015 |
Ernouf G, Brayer JL, Folléas B, Demoute JP, Meyer C, Cossy J. Synthesis of Functionalized Alkylidenecyclopropanes by Ireland-Claisen Rearrangement of Cyclopropenylcarbinyl Esters. Organic Letters. 17: 3786-9. PMID 26186488 DOI: 10.1021/Acs.Orglett.5B01759 |
0.626 |
|
2015 |
Brioche J, Meyer C, Cossy J. Synthesis of 2-aminoindolizines by 1,3-dipolar cycloaddition of pyridinium ylides with electron-deficient ynamides. Organic Letters. 17: 2800-3. PMID 25988320 DOI: 10.1021/Acs.Orglett.5B01205 |
0.803 |
|
2015 |
Specklin S, Boissonnat G, Lecourt C, Sorin G, Lannou MI, Ardisson J, Sautel F, Massiot G, Meyer C, Cossy J. Synthetic Studies toward the C32-C46 Segment of Hemicalide. Assignment of the Relative Configuration of the C36-C42 Subunit. Organic Letters. 17: 2446-9. PMID 25906322 DOI: 10.1021/Acs.Orglett.5B00955 |
0.461 |
|
2015 |
Archambeau A, Miege F, Meyer C, Cossy J. Intramolecular cyclopropanation and C-H insertion reactions with metal carbenoids generated from cyclopropenes. Accounts of Chemical Research. 48: 1021-31. PMID 25763601 DOI: 10.1021/Acs.Accounts.5B00016 |
0.576 |
|
2014 |
De Gussem E, Herrebout W, Specklin S, Meyer C, Cossy J, Bultinck P. Strength by joining methods: combining synthesis with NMR, IR, and vibrational circular dichroism spectroscopy for the determination of the relative configuration in hemicalide. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 17385-94. PMID 25346258 DOI: 10.1002/Chem.201404822 |
0.438 |
|
2014 |
Krieger JP, Ricci G, Lesuisse D, Meyer C, Cossy J. Efficient and modular synthesis of new structurally diverse functionalized [n]paracyclophanes by a ring-distortion strategy. Angewandte Chemie (International Ed. in English). 53: 8705-8. PMID 24981087 DOI: 10.1002/Anie.201401070 |
0.521 |
|
2013 |
Sorin G, Fleury E, Tran C, Prost E, Molinier N, Sautel F, Massiot G, Specklin S, Meyer C, Cossy J, Lannou MI, Ardisson J. Synthetic studies on hemicalide: development of a convergent approach toward the C1-C25 fragment. Organic Letters. 15: 4734-7. PMID 24001374 DOI: 10.1021/Ol402077E |
0.434 |
|
2013 |
de Carné-Carnavalet B, Meyer C, Cossy J, Folléas B, Brayer JL, Demoute JP. A Sonogashira cross-coupling/5-exo-dig cyclization/ionic hydrogenation sequence: synthesis of 4-substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides. The Journal of Organic Chemistry. 78: 5794-9. PMID 23638839 DOI: 10.1021/Jo400713U |
0.575 |
|
2013 |
Brioche J, Meyer C, Cossy J. Synthesis of functionalized allenamides from ynamides by enolate Claisen rearrangement. Organic Letters. 15: 1626-9. PMID 23496162 DOI: 10.1021/Ol400402N |
0.813 |
|
2012 |
de Carné-Carnavalet B, Archambeau A, Meyer C, Cossy J, Folléas B, Brayer JL, Demoute JP. Efficient synthesis of substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides using a copper-free Sonogashira coupling. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 16716-27. PMID 23180687 DOI: 10.1002/Chem.201203153 |
0.628 |
|
2012 |
Archambeau A, Miege F, Meyer C, Cossy J. Highly efficient stereoselective catalytic C(sp3)-H insertions with donor rhodium carbenoids generated from cyclopropenes. Angewandte Chemie (International Ed. in English). 51: 11540-4. PMID 23042749 DOI: 10.1002/Anie.201205913 |
0.516 |
|
2012 |
Miege F, Meyer C, Cossy J. Gold(I)-catalysed cycloisomerisation of 1,6-cyclopropene-enes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 7810-22. PMID 22588697 DOI: 10.1002/Chem.201200566 |
0.578 |
|
2012 |
Druais V, Meyer C, Cossy J. Catalytic diastereoselective reduction of α,β-epoxy and α,β-aziridinyl ynones. Organic Letters. 14: 516-9. PMID 22217034 DOI: 10.1021/Ol203114A |
0.407 |
|
2011 |
Miege F, Meyer C, Cossy J. When cyclopropenes meet gold catalysts. Beilstein Journal of Organic Chemistry. 7: 717-34. PMID 21804867 DOI: 10.3762/Bjoc.7.82 |
0.416 |
|
2011 |
Miege F, Meyer C, Cossy J. Rhodium-catalyzed cycloisomerization involving cyclopropenes: efficient stereoselective synthesis of medium-sized heterocyclic scaffolds. Angewandte Chemie (International Ed. in English). 50: 5932-7. PMID 21567678 DOI: 10.1002/Anie.201101220 |
0.605 |
|
2011 |
Trigili C, Pera B, Barbazanges M, Cossy J, Meyer C, Pineda O, Rodríguez-Escrich C, Urpí F, Vilarrasa J, Díaz JF, Barasoain I. Mechanism of action of the cytotoxic macrolides amphidinolide X and J. Chembiochem : a European Journal of Chemical Biology. 12: 1027-30. PMID 21500335 DOI: 10.1002/Cbic.201100042 |
0.373 |
|
2011 |
Barbazanges M, Meyer C, Cossy J, Turner P. Synthesis of 1,2-amino alcohols by sigmatropic rearrangements of 3-(N-tosylamino)allylic alcohol derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 4480-95. PMID 21337437 DOI: 10.1002/Chem.201003265 |
0.564 |
|
2011 |
de Carné-Carnavalet B, Archambeau A, Meyer C, Cossy J, Folléas B, Brayer JL, Demoute JP. Copper-free Sonogashira coupling of cyclopropyl iodides with terminal alkynes. Organic Letters. 13: 956-9. PMID 21268662 DOI: 10.1021/Ol1029996 |
0.511 |
|
2010 |
Miege F, Meyer C, Cossy J. Synthesis of 3-oxa- and 3-azabicyclo[4.1.0]heptanes by gold-catalyzed cycloisomerization of cyclopropenes. Organic Letters. 12: 4144-7. PMID 20726564 DOI: 10.1021/Ol101741F |
0.651 |
|
2010 |
Miege F, Meyer C, Cossy J. Ring-rearrangement metathesis of cyclopropenes: synthesis of heterocycles. Organic Letters. 12: 248-51. PMID 19994906 DOI: 10.1021/Ol9025606 |
0.617 |
|
2010 |
Cossy J, Lutz F, Alauze V, Meyer C. ChemInform Abstract: Carbon-Carbon Bond Forming Reactions Using Bistrifluoromethanesulfonimide. Cheminform. 33: no-no. DOI: 10.1002/chin.200218082 |
0.406 |
|
2010 |
LAUTENS M, MEYER C, LORENZ A. ChemInform Abstract: Ring Opening in the Hydrostannation of Methylenecyclopropanes: Effect of the Catalyst and Substrate. Cheminform. 28: no-no. DOI: 10.1002/chin.199708178 |
0.357 |
|
2009 |
Cantagrel G, de Carné-Carnavalet B, Meyer C, Cossy J. Iron trichloride-promoted cyclization of o-alkynylaryl isocyanates: synthesis of 3-(chloromethylene)oxindoles. Organic Letters. 11: 4262-5. PMID 19739609 DOI: 10.1021/Ol9014877 |
0.555 |
|
2009 |
Druais V, Hall MJ, Corsi C, Wendeborn SV, Meyer C, Cossy J. A convergent approach toward the C1-C11 subunit of phoslactomycins and formal synthesis of phoslactomycin B. Organic Letters. 11: 935-8. PMID 19170620 DOI: 10.1021/Ol8029142 |
0.496 |
|
2009 |
Couty S, Meyer C, Cossy J. Gold-catalyzed cycloisomerizations of ene-ynamides Tetrahedron. 65: 1809-1832. DOI: 10.1016/J.Tet.2008.10.108 |
0.572 |
|
2009 |
Lorthiois E, Meyer C. Carbozincation of Alkenes and Alkynes Patai's Chemistry of Functional Groups. 863-978. DOI: 10.1002/9780470682531.Pat0382 |
0.466 |
|
2008 |
Barbazanges M, Meyer C, Cossy J. Total synthesis of amphidinolide J. Organic Letters. 10: 4489-92. PMID 18811171 DOI: 10.1021/Ol801708X |
0.587 |
|
2008 |
Barbazanges M, Meyer C, Cossy J. Synthesis of optically enriched 1,2-aminoalcohols by [2,3]-Wittig rearrangements of 3-aza-allylic alcohol derivatives Tetrahedron Letters. 49: 2902-2906. DOI: 10.1016/J.Tetlet.2008.03.023 |
0.539 |
|
2008 |
Salit AF, Meyer C, Cossy J, Delouvrié B, Hennequin L. Synthetic studies toward cytostatin, a natural product inhibitor of protein phosphatase 2A Tetrahedron. 64: 6684-6697. DOI: 10.1016/J.Tet.2008.05.012 |
0.511 |
|
2007 |
Barbazanges M, Meyer C, Cossy J. Stereoselective synthesis of 1,2-aminoalcohols by [2,3]-wittig rearrangements Organic Letters. 9: 3245-3248. PMID 17655314 DOI: 10.1021/Ol0711725 |
0.547 |
|
2007 |
Amans D, Flohic AL, Bellosta V, Meyer C, Cossy J. Synthesis of an analog of mycothiazole and total synthesis of pseudotrienic acid B Pure and Applied Chemistry. 79: 677-684. DOI: 10.1351/Pac200779040677 |
0.597 |
|
2007 |
Cantagrel G, Meyer C, Cossy J. Synthetic studies towards the marine natural product palmerolide A: Synthesis of the C3-C15 and C16-C23 fragments Synlett. 2983-2986. DOI: 10.1055/S-2007-992366 |
0.437 |
|
2007 |
Couty S, Meyer C, Cossy J. Chemoselective epoxidation of ene-ynamides: Intramolecular cyclopropanation induced by the intermediate α-oxocarbene Synlett. 2819-2822. DOI: 10.1055/S-2007-990841 |
0.476 |
|
2007 |
Salit AF, Meyer C, Cossy J. Formal synthesis of cytostatin by a convergent approach Synlett. 934-938. DOI: 10.1055/S-2007-970786 |
0.487 |
|
2006 |
Couty S, Meyer C, Cossy J. Diastereoselective gold-catalyzed cycloisomerizations of ene-ynamides. Angewandte Chemie (International Ed. in English). 45: 6726-30. PMID 16986188 DOI: 10.1002/Anie.200602270 |
0.571 |
|
2006 |
Couty S, Meyer C, Cossy J. A Short Synthesis of Lennoxamine via Ynamides. Cheminform. 37. DOI: 10.1016/J.Tetlet.2005.11.093 |
0.644 |
|
2006 |
Flohic AL, Meyer C, Cossy J. Reactivity of unsaturated sultones synthesized from unsaturated alcohols by ring-closing metathesis. Application to the racemic synthesis of the originally proposed structure of mycothiazole Tetrahedron. 62: 9017-9037. DOI: 10.1016/J.Tet.2006.07.010 |
0.61 |
|
2006 |
Couty S, Liegault B, Meyer C, Cossy J. Synthesis of 3-(Arylmethylene)isoindolin-1-ones from Ynamides by Heck—Suzuki—Miyaura Domino Reactions. Application to the Synthesis of Lennoxamine. Cheminform. 37. DOI: 10.1016/J.Tet.2005.11.089 |
0.655 |
|
2005 |
Le Flohic A, Meyer C, Cossy J. Total synthesis of (+/-)-mycothiazole and formal enantioselective approach. Organic Letters. 7: 339-42. PMID 15646992 DOI: 10.1021/Ol047603Q |
0.65 |
|
2005 |
Cossy J, Meyer C, Defosseux M, Blanchard N. Total synthesis of zincophorin Pure and Applied Chemistry. 77: 1131-1137. DOI: 10.1351/Pac200577071131 |
0.774 |
|
2005 |
Defosseux M, Blanchard N, Meyer C, Cossy J. Synthesis of polypropionate subunits from cyclopropanes Tetrahedron. 61: 7632-7653. DOI: 10.1016/J.Tet.2005.05.099 |
0.749 |
|
2004 |
Couty S, Liégault B, Meyer C, Cossy J. Heck-Suzuki-Miyaura domino reactions involving ynamides. An efficient access to 3-(arylmethylene)isoindolinones. Organic Letters. 6: 2511-4. PMID 15255678 DOI: 10.1021/Ol049302M |
0.61 |
|
2004 |
Defosseux M, Blanchard N, Meyer C, Cossy J. Total synthesis of zincophorin and its methyl ester. The Journal of Organic Chemistry. 69: 4626-47. PMID 15230584 DOI: 10.1021/Jo0496042 |
0.744 |
|
2004 |
Taillier C, Bellosta V, Meyer C, Cossy J. Synthesis of omega-hydroxy ketones from omega-benzyloxy Weinreb amides by using a chemoselective nucleophilic addition/Birch reduction process. Organic Letters. 6: 2145-7. PMID 15200306 DOI: 10.1021/Ol049434F |
0.636 |
|
2004 |
Meyer C, Defosseux M, Blanchard N, Cossy J. Chapter 10 Total synthesis of zincophorin and its methyl ester Strategies and Tactics in Organic Synthesis. 5: 303-352. DOI: 10.1016/S1874-6004(04)80033-9 |
0.767 |
|
2004 |
Le Flohic A, Meyer C, Cossy J, Desmurs J. Synthesis of Unsaturated [1,2]Oxazines by Using Sigmatropic Rearrangements and the Ring-Closing Metathesis Reaction. Cheminform. 35. DOI: 10.1016/J.Tetlet.2003.09.125 |
0.66 |
|
2003 |
Defosseux M, Blanchard N, Meyer C, Cossy J. Total synthesis of zincophorin methyl ester. Organic Letters. 5: 4037-40. PMID 14572243 DOI: 10.1021/Ol035177N |
0.754 |
|
2003 |
Meyer C, Blanchard N, Defosseux M, Cossy J. Stereoselective synthesis of polypropionate units and heterocyclic compounds by cyclopropylcarbinol ring-opening with mercury(II) salts. Accounts of Chemical Research. 36: 766-72. PMID 14567710 DOI: 10.1021/Ar020154E |
0.772 |
|
2003 |
Flohic AL, Meyer C, Cossy J, Desmurs J, Galland J. Unsaturated Sultones from Unsaturated Sulfonates: Synthesis by Ring-Closing Metathesis and Reactivity Synlett. 2003: 667-670. DOI: 10.1055/S-2003-38363 |
0.617 |
|
2003 |
Pevet I, Meyer C, Cossy J. [2,3]-Wittig Sigmatropic Rearrangement of γ-Allyloxy-β-enaminoesters. Cheminform. 34. DOI: 10.1055/S-2003-38362 |
0.391 |
|
2003 |
His S, Meyer C, Cossy J, Emeric G, Greiner A. Solid phase synthesis of amides by the Beckmann rearrangement of ketoxime carbonates Tetrahedron Letters. 44: 8581-8584. DOI: 10.1016/J.Tetlet.2003.09.113 |
0.547 |
|
2002 |
Cossy J, Blanchard N, Defosseux M, Meyer C. A synthetic approach towards the C1-C9 subunit of zincophorin. Angewandte Chemie (International Ed. in English). 41: 2144-6. PMID 19746623 DOI: 10.1002/1521-3773(20020617)41:12<2144::Aid-Anie2144>3.0.Co;2-E |
0.679 |
|
2002 |
Cossy J, Lutz F, Alauze V, Meyer C. Carbon-Carbon Bond Forming Reactions by using Bistrifluoromethanesulfonimide Synlett. 2002: 0045-0048. DOI: 10.1055/S-2002-19329 |
0.551 |
|
2002 |
Cossy J, Blanchard N, Meyer C. Stereoselective oxymercuration of cyclopropylcarbinols with anchimeric assistance by aromatic groups Tetrahedron Letters. 43: 1801-1805. DOI: 10.1016/S0040-4039(02)00069-2 |
0.725 |
|
2001 |
Cossy J, Blanchard N, Meyer C. Synthesis of stereotriads by oxymercuration of substituted cyclopropylcarbinols. Organic Letters. 3: 2567-9. PMID 11483062 DOI: 10.1021/Ol0162365 |
0.754 |
|
2001 |
Cossy J, Defosseux M, Meyer C. Diastereoselective Synthesis of Homopropargylic Alcohols on Solid Support Synlett. 2001: 0815-0817. DOI: 10.1055/S-2001-14599 |
0.525 |
|
2001 |
Pévet I, Meyer C, Cossy J. [2,3]-Wittig rearrangement of γ-allyloxy-β-ketoesters. A new access to tetronic acids Tetrahedron Letters. 42: 5215-5218. DOI: 10.1016/S0040-4039(01)00982-0 |
0.458 |
|
2001 |
Cossy J, Pévet I, Meyer C. Total Synthesis of (−)‐4a,5‐Dihydrostreptazolin European Journal of Organic Chemistry. 2001: 2841-2850. DOI: 10.1002/1099-0690(200108)2001:15<2841::Aid-Ejoc2841>3.0.Co;2-W |
0.586 |
|
2001 |
Cossy J, Blanchard N, Meyer C. Synthesis of isopropenylcyclopropanes - Revision of the relative configuration of cyclopropyl ketones obtained by 1,3-elimination of γ-epoxy ketones European Journal of Organic Chemistry. 339-348. DOI: 10.1002/1099-0690(200101)2001:2<339::Aid-Ejoc339>3.0.Co;2-J |
0.78 |
|
2000 |
Cossy J, Pévet I, Meyer C. A Short and Efficient Synthesis of (-)-4a,5-Dihydrostreptazolin Synlett. 2000: 122-124. DOI: 10.1055/S-2000-6433 |
0.497 |
|
1999 |
Cossy J, Blanchard N, Hamel C, Meyer C. Diastereoselective Hydroboration of Isopropenylcyclopropanes. The Journal of Organic Chemistry. 64: 2608-2609. PMID 11674323 DOI: 10.1021/Jo990001D |
0.782 |
|
1999 |
Cossy J, Blanchard N, Meyer C. Stereoselective synthesis of cyclopropanes bearing adjacent stereocenters Synthesis. 1063-1075. DOI: 10.1055/S-1999-3507 |
0.782 |
|
1999 |
Cossy J, Blanchard N, Meyer C. Diastereoselectivity in the dihydroxylation of isopropenyl substituted three-membered rings Tetrahedron Letters. 40: 8361-8364. DOI: 10.1016/S0040-4039(99)01727-X |
0.759 |
|
1998 |
Cossy J, Blanchard N, Meyer C. Directing Effect of a Neighboring Aromatic Group in the Cyclopropanation of Allylic Alcohols. The Journal of Organic Chemistry. 63: 5728-5729. PMID 11672161 DOI: 10.1021/Jo9806815 |
0.695 |
|
1997 |
Meyer C, Cossy J. Synthesis of oxygenated heterocycles from cyclic allylsiloxanes using ring-closing olefin metathesis Tetrahedron Letters. 38: 7861-7864. DOI: 10.1016/S0040-4039(97)10147-2 |
0.653 |
|
1997 |
Lautens M, Meyer C, van Oeveren A. Synthesis and reactions of 1,2-disubstituted methylenecyclopropanes prepared via intramolecular cyclopropanation of allenic diazoacetates Tetrahedron Letters. 38: 3833-3836. DOI: 10.1016/S0040-4039(97)00765-X |
0.505 |
|
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 |
0.767 |
|
1996 |
Meyer C, Piva O, Pete J. Competition between intramolecular [2+2] photocycloaddition and hydrogen-abstraction reactions from 2-carboxamidocyclopent-2-enones Tetrahedron Letters. 37: 5885-5888. DOI: 10.1016/0040-4039(96)01268-3 |
0.41 |
|
1996 |
Meyer C, Marek I, Normant JF. Stereoselective synthesis of linear and angular triquinanes skeletons via the zinca-ene-allene reactions Tetrahedron Letters. 37: 857-860. DOI: 10.1016/0040-4039(95)02325-9 |
0.704 |
|
1996 |
Lautens M, Kumanovic S, Meyer C. Heterogeneous Palladium-Catalyzed Regioselective Hydrostannation of Alkenes Angewandte Chemie International Edition in English. 35: 1329-1330. DOI: 10.1002/Anie.199613291 |
0.509 |
|
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 |
0.814 |
|
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 |
0.798 |
|
1993 |
Meyer C, Marek I, Courtemanche G, Normant JF. Intramolecular carbometallation of secondary organozinc reagents. Tetrahedron Letters. 34: 6053-6056. DOI: 10.1016/S0040-4039(00)61725-2 |
0.717 |
|
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