Year |
Citation |
Score |
2015 |
Olszewski TK, Majewski M. Highly diastereoselective addition of chiral H-phosphonate to tert-butylsulfinyl aldimines: a convenient approach to (R)-α-aminophosphonic acids Tetrahedron Asymmetry. 26: 846-852. DOI: 10.1016/j.tetasy.2015.06.008 |
0.339 |
|
2014 |
Savela R, Majewski M, Leino R. Iron-catalyzed arylation of aromatic ketones and aldehydes mediated by organosilanes European Journal of Organic Chemistry. 2014: 4137-4147. DOI: 10.1002/ejoc.201402023 |
0.388 |
|
2012 |
Palyam N, Niewczas I, Majewski M. Stereodivergent synthesis of D,D- and L,L-glycero-β-alloa- heptopyranoses on a dioxanone scaffold Synlett. 23: 2367-2370. DOI: 10.1055/S-0032-1290461 |
0.711 |
|
2010 |
Majewski M. ChemInform Abstract: Enantioselective Deprotonation of Cyclic Ketones Cheminform. 30: no-no. DOI: 10.1002/chin.199928319 |
0.368 |
|
2009 |
Palyam N, Majewski M. Organocatalytic syn-aldol reactions of dioxanones with (S)-isoserinal hydrate: synthesis of L-deoxymannojirimycin and L-deoxyidonojirimycin. The Journal of Organic Chemistry. 74: 4390-2. PMID 19405512 DOI: 10.1021/Jo900263S |
0.708 |
|
2009 |
Green JR, Alo BI, Majewski M, Snieckus V. γ-Silylated α,β-unsaturated amides — Preparation by [1,5]-sigmatropic rearrangement and use as masked dienolate equivalents in carbonyl condensations Canadian Journal of Chemistry. 87: 745-759. DOI: 10.1139/V09-054 |
0.308 |
|
2009 |
Green JR, Alo BI, Majewski M, Snieckus V. ChemInform Abstract: γ-Silylated α,β-Unsaturated Amides â Preparation by [1,5]-Sigmatropic Rearrangement and Use as Masked Dienolate Equivalents in Carbonyl Condensations. Cheminform. 40. DOI: 10.1002/CHIN.200950079 |
0.306 |
|
2008 |
Niewczas I, Majewski M. Building Higher Carbohydrates via Dioxanone Aldol Chemistry: The α,α′-Bisaldol Approach European Journal of Organic Chemistry. 2009: 33-37. DOI: 10.1002/Ejoc.200800844 |
0.51 |
|
2007 |
Palyam N, Niewczas I, Majewski M. Building carbohydrates on the dioxanone scaffold: stereoselective synthesis of d-glycero-d-manno-2-octulose Tetrahedron Letters. 48: 9195-9198. DOI: 10.1016/J.Tetlet.2007.10.100 |
0.703 |
|
2006 |
Majewski M, Ulaczyk-Lesanko A, Wang F. Chiral lithium amides on polymer support Synthesis and use in deprotonation of ketones Canadian Journal of Chemistry. 84: 257-268. DOI: 10.1139/V06-006 |
0.404 |
|
2006 |
Majewski M, Niewczas I, Palyam N. Acids as proline co-catalysts in the aldol reaction of 1,3-dioxan-5-ones Synlett. 2006: 2387-2390. DOI: 10.1055/S-2006-950421 |
0.69 |
|
2005 |
Majewski M. Organolithiums in Enantioselective Synthesis Advanced Synthesis & Catalysis. 347: 719-720. DOI: 10.1002/Adsc.200404329 |
0.498 |
|
2002 |
Majewski M, Wang F. Are there concentration effects in enantioselective deprotonation of cyclic ketones Tetrahedron. 58: 4567-4571. DOI: 10.1016/S0040-4020(02)00363-0 |
0.407 |
|
2001 |
Majewski M, DeCaire M, Nowak P, Wang F. Studies on enolate chemistry of 8-thiabicyclo[3.2.1]- octan-3-one: enantioselective deprotonation and synthesis of sulfur analogs of tropane alkaloids Canadian Journal of Chemistry. 79: 1792-1798. DOI: 10.1139/V01-157 |
0.504 |
|
2000 |
Majewski M, Nowak P. Aldol addition of lithium and boron enolates of 1,3-dioxan-5-ones to aldehydes. A new entry into monosaccharide derivatives Journal of Organic Chemistry. 65: 5152-5160. PMID 10993340 DOI: 10.1021/Jo0002238 |
0.409 |
|
2000 |
Majewski M, DeCaire M, Nowak P, Wang F. ChemInform Abstract: Enolates of Thiabicyclic Ketones as Stepping Stones Towards Synthesis of Sulfur Analogues of Tropane Alkaloids. Cheminform. 31: no-no. DOI: 10.1002/chin.200048177 |
0.413 |
|
1999 |
Majewski M, Nowak P. Stereoselective Synthesis Of Protected Ketohexoses Via Aldol Reaction Of Chiral Dioxanone Enolate Synlett. 1999: 1447-1449. DOI: 10.1055/S-1999-2862 |
0.55 |
|
1999 |
Majewski M, Ulaczyk A, Wang F. Chiral lithium amides on solid support: synthesis and applications in enantioselective deprotonation of cyclic ketones Tetrahedron Letters. 40: 8755-8758. DOI: 10.1016/S0040-4039(99)01882-1 |
0.462 |
|
1998 |
Majewski M, Nowak P. Stereoselective synthesis of (+)-frontalin Tetrahedron-Asymmetry. 9: 2611-2617. DOI: 10.1016/S0957-4166(98)00263-8 |
0.451 |
|
1998 |
Majewski M, Shao J, Nelson K, Nowak P, Irvine NM. Stereoselective synthesis of hydroxyindolizidines via sparteine-assisted deprotonation of N-Boc-pyrrolidine Tetrahedron Letters. 39: 6787-6790. DOI: 10.1016/S0040-4039(98)01491-9 |
0.519 |
|
1998 |
Majewski M, Nowak P. Rate of deprotonation of a simple ketone by lithium diisopropylamide Tetrahedron Letters. 39: 1661-1664. DOI: 10.1016/S0040-4039(98)00015-X |
0.358 |
|
1997 |
Majewski M, Lazny R, Ulaczyk A. Enantioselective ring opening of tropinone. A new entry into tropane alkaloids Canadian Journal of Chemistry. 75: 754-761. DOI: 10.1139/V97-091 |
0.518 |
|
1996 |
Majewski M, Lazny R. Stereoselective Synthesis of Tropane Alkaloids: Physoperuvine and Dihydroxytropanes Synlett. 1996: 785-786. DOI: 10.1055/S-1996-5532 |
0.489 |
|
1995 |
Majewski M, Gleave DM, Nowak P. 1,3-Dioxan-5-ones: synthesis, deprotonation, and reactions of their lithium enolates Canadian Journal of Chemistry. 73: 1616-1626. DOI: 10.1139/V95-201 |
0.532 |
|
1995 |
Majewski M, Irvine NM, Zook SE. Reactions Of Verbenone Dienolate With Aromatic Aldehydes Synthetic Communications. 25: 3237-3246. DOI: 10.1080/00397919508015475 |
0.454 |
|
1995 |
Irvine NM, Majewski M. Synthesis Of 1,3-Dimethylazulene Organic Preparations and Procedures International. 27: 592-595. DOI: 10.1080/00304949509458513 |
0.45 |
|
1995 |
Majewski M, Lazny R. Synthesis Of Tropane Alkaloids Via Enantioselective Deprotonation Of Tropinone Journal of Organic Chemistry. 60: 5825-5830. DOI: 10.1021/Jo00123A018 |
0.39 |
|
1995 |
Majewski M, Irvine NM, MacKinnon J. Synthesis of butenolides via enantioselective deprotonation of protected 4-hydroxycyclohexanone Tetrahedron-Asymmetry. 6: 1837-1840. DOI: 10.1016/0957-4166(95)00231-D |
0.432 |
|
1995 |
Majewski M, Lazny R, Nowak P. Effect Of Lithium Salts On Enantioselective Deprotonation Of Cyclic Ketones Tetrahedron Letters. 36: 5465-5468. DOI: 10.1016/0040-4039(95)01056-N |
0.446 |
|
1994 |
Majewski M, MacKinnon J. Enantioselective deprotonation of protected 4-hydroxycyclohexanones Canadian Journal of Chemistry. 72: 1699-1704. DOI: 10.1139/V94-214 |
0.42 |
|
1994 |
Majewski M, Irvine NM, Bantle GW. Stereoselective Synthesis Of Dimethylrobustadials Journal of Organic Chemistry. 59: 6697-6702. DOI: 10.1021/Jo00101A031 |
0.483 |
|
1994 |
Majewski M, Lazny R. Synthesis of pyranotropanes via enantioselective deprotonation strategy Tetrahedron Letters. 35: 3653-3656. DOI: 10.1016/S0040-4039(00)73063-2 |
0.474 |
|
1994 |
Majewski M, Gleave DM. Reduction with lithium dialkylamides Journal of Organometallic Chemistry. 470: 1-16. DOI: 10.1016/0022-328X(94)80142-8 |
0.426 |
|
1992 |
Majewski M, Bantle GW. Synthesis of 3,4-Dihydrospiro[2H-1-Benzopyran-2,2′-bicyclo[2.2.1]heptane] Ring System Synthetic Communications. 22: 23-33. DOI: 10.1080/00397919208021075 |
0.407 |
|
1992 |
Majewski M, Gleave DM. Enantioselective formation of cis-3,5-dimethylcyclohexanone lithium enolate and stereoselective aldol reaction with benzaldehyde Journal of Organic Chemistry. 57: 3599-3605. DOI: 10.1021/Jo00039A018 |
0.473 |
|
1991 |
Majewski M, Zheng G. Enantioselective Deprotonation of Tropinone and Reactions of Tropinone Lithium Enolate Synlett. 1991: 173-175. DOI: 10.1055/S-1991-20667 |
0.552 |
|
1990 |
Majewski M, Bantle GW. Reactions of β-Pinene with Aromatic Aldehydes Synthetic Communications. 20: 2549-2558. DOI: 10.1080/00397919008053204 |
0.482 |
|
1990 |
Clive DLJ, Murthy KSK, Wee AGH, Prasad JS, Da Silva GVJ, Majewski M, Anderson PC, Evans CF, Haugen RD. Total synthesis of both (+)-compactin and (+)-mevinolin. A general strategy based on the use of a special titanium reagent for dicarbonyl coupling Journal of the American Chemical Society. 112: 3018-3028. DOI: 10.1021/Ja00164A024 |
0.303 |
|
1989 |
Majewski M, Gleave DM. Diastereoselective aldol reactions of cyclohexanone lithium enolate Tetrahedron Letters. 30: 5681-5684. DOI: 10.1016/S0040-4039(00)76169-7 |
0.498 |
|
1989 |
Majewski M, Bantle G. Stereoselective construction of the ring system of robustadials Tetrahedron Letters. 30: 6653-6656. DOI: 10.1016/S0040-4039(00)70642-3 |
0.482 |
|
1988 |
Majewski M. Lithium diisopropylamide as a hydride donor. Reduction of aldehydes. Tetrahedron Letters. 29: 4057-4060. DOI: 10.1016/S0040-4039(00)80416-5 |
0.339 |
|
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