| Year |
Citation |
Score |
| 2017 |
Rarig RF, Nelson JM, Vedejs E. Synthesis of a Nonracemic C2 Symmetric Tetrahydro-1,4-azaborine and Evaluation of Hydroboration Enantioselectivity. The Journal of Organic Chemistry. PMID 29110479 DOI: 10.1021/acs.joc.7b01904 |
0.765 |
|
| 2017 |
Kinens A, Sejejs M, Kamlet AS, Piotrowski DW, Vedejs E, Suna E. Development of a Chiral DMAP Catalyst for the Dynamic Kinetic Resolution of Azole Hemiaminals. The Journal of Organic Chemistry. PMID 28060519 DOI: 10.1021/Acs.Joc.6B02955 |
0.302 |
|
| 2015 |
Peris G, Vedejs E. Enantiocontrolled synthesis of a tetracyclic aminal corresponding to the core subunit of diazonamide A. The Journal of Organic Chemistry. 80: 3050-7. PMID 25705992 DOI: 10.1021/Jo502939A |
0.68 |
|
| 2013 |
Prokofjevs A, Jermaks J, Borovika A, Kampf JW, Vedejs E. Electrophilic C-H Borylation and Related Reactions of B-H Boron Cations. Organometallics. 32. PMID 24347788 DOI: 10.1021/Om400651P |
0.806 |
|
| 2013 |
Cazorla C, De Vries TS, Vedejs E. P-directed borylation of phenols. Organic Letters. 15: 984-7. PMID 23363045 DOI: 10.1021/Ol303203M |
0.377 |
|
| 2012 |
De Vries TS, Majumder S, Sandelin AM, Wang G, Vedejs E. Mechanistic variations in ionic hydrogenation of unsaturated phosphine and amine boranes. Organic Letters. 14: 688-91. PMID 22251083 DOI: 10.1021/Ol2031203 |
0.343 |
|
| 2012 |
Wiedner SD, Vedejs E. Reactivity of aziridinomitosene derivatives related to FK317 in the presence of protic nucleophiles. The Journal of Organic Chemistry. 77: 1045-55. PMID 22208619 DOI: 10.1021/Jo202286A |
0.788 |
|
| 2011 |
Vedejs E. Review of Enantioselective Chemical Synthesis: Methods, Logic and Practice Journal of the American Chemical Society. 133: 3686-3686. DOI: 10.1021/Ja2011127 |
0.315 |
|
| 2010 |
Nelson JM, Vedejs E. Metalated aziridines for cross-coupling with aryl and alkenyl halides via palladium catalysis. Organic Letters. 12: 5085-7. PMID 20945857 DOI: 10.1021/Ol101904A |
0.373 |
|
| 2010 |
Wiedner SD, Vedejs E. Aziridinomitosanes via lactam cyclization. Organic Letters. 12: 4030-3. PMID 20738104 DOI: 10.1021/Ol101595U |
0.806 |
|
| 2010 |
Duffey TA, Mackay JA, Vedejs E. Catalytic parallel kinetic resolution under homogeneous conditions. The Journal of Organic Chemistry. 75: 4674-85. PMID 20557113 DOI: 10.1021/Jo100695Z |
0.765 |
|
| 2010 |
Vedejs E, Daugulis O. ChemInform Abstract: Chiral Phosphines as Enantioselective Acylating Agents; Phosphorus Configuration and the Search for Reactive Catalysts Cheminform. 30: no-no. DOI: 10.1002/chin.199949231 |
0.584 |
|
| 2009 |
Wang G, Vedejs E. Stereocontrol in N-directed hydroboration: synthesis of amino alcohols related to the piperidine alkaloids. Organic Letters. 11: 1059-61. PMID 19182927 DOI: 10.1021/Ol802781C |
0.396 |
|
| 2009 |
Duffey TA, Shaw SA, Vedejs E. AcOLeDMAP and BnOLeDMAP: conformationally restricted nucleophilic catalysts for enantioselective rearrangement of indolyl acetates and carbonates. Journal of the American Chemical Society. 131: 14-5. PMID 19093886 DOI: 10.1021/Ja805541U |
0.71 |
|
| 2008 |
Karatjas AG, Vedejs E. Formation of pinacol boronate esters via pyridine iodoborane hydroboration. The Journal of Organic Chemistry. 73: 9508-10. PMID 19007135 DOI: 10.1021/Jo8020049 |
0.435 |
|
| 2008 |
Rarig RA, Scheideman M, Vedejs E. Oxygen-directed intramolecular hydroboration. Journal of the American Chemical Society. 130: 9182-3. PMID 18572941 DOI: 10.1021/Ja800402G |
0.761 |
|
| 2008 |
Scheideman M, Wang G, Vedejs E. Amine-directed hydroboration: scope and limitations. Journal of the American Chemical Society. 130: 8669-76. PMID 18549217 DOI: 10.1021/Ja0774663 |
0.783 |
|
| 2008 |
Peris G, Vedejs E. Diastereoselective carboxyl migrations of 3-arylbenzofuranones. The Journal of Organic Chemistry. 73: 1158-61. PMID 18179233 DOI: 10.1021/Jo7021444 |
0.642 |
|
| 2008 |
Clay JM, Karatjas AG, Vedejs E. Hydroboration with pyridine borane at room temperature (Journal of the American Chemical Society (2005) 127 (5166-5167)) Journal of the American Chemical Society. 130: 10828. DOI: 10.1021/ja8046602 |
0.733 |
|
| 2007 |
Warner DL, Hibberd AM, Kalman M, Klapars A, Vedejs E. N-silyl protecting groups for labile aziridines: application toward the synthesis of N-H aziridinomitosenes. The Journal of Organic Chemistry. 72: 8519-22. PMID 17910500 DOI: 10.1021/Jo7013615 |
0.804 |
|
| 2007 |
Bobeck DR, Warner DL, Vedejs E. Internal azomethine ylide cycloaddition methodology for access to the substitution pattern of aziridinomitosene A. The Journal of Organic Chemistry. 72: 8506-18. PMID 17910499 DOI: 10.1021/Jo7013559 |
0.812 |
|
| 2006 |
Shapland P, Vedejs E. Isopinocampheylborane derivatives with >99% ee via the DMAP complex. The Journal of Organic Chemistry. 71: 6666-9. PMID 16901168 DOI: 10.1021/Jo061002Q |
0.342 |
|
| 2006 |
Shaw SA, Aleman P, Christy J, Kampf JW, Va P, Vedejs E. Enantioselective TADMAP-catalyzed carboxyl migration reactions for the synthesis of stereogenic quaternary carbon. Journal of the American Chemical Society. 128: 925-34. PMID 16417383 DOI: 10.1021/Ja056150X |
0.316 |
|
| 2006 |
MacKay JA, Vedejs E. Synthesis and reactivity of new chiral bicyclic phospholanes as acyl-transfer catalysts. The Journal of Organic Chemistry. 71: 498-503. PMID 16408956 DOI: 10.1021/Jo0519155 |
0.605 |
|
| 2005 |
Rink SM, Warner DL, Klapars A, Vedejs E. Sequence-specific DNA interstrand cross-linking by an aziridinomitosene in the absence of exogenous reductant. Biochemistry. 44: 13981-6. PMID 16229487 DOI: 10.1021/Bi050426W |
0.759 |
|
| 2005 |
Atkins JM, Vedejs E. A two-stage iterative process for the synthesis of poly-oxazoles. Organic Letters. 7: 3351-4. PMID 16018658 DOI: 10.1021/Ol051244X |
0.424 |
|
| 2005 |
Vedejs E, Jure M. Efficiency in nonenzymatic kinetic resolution. Angewandte Chemie (International Ed. in English). 44: 3974-4001. PMID 15942973 DOI: 10.1002/Anie.200460842 |
0.348 |
|
| 2005 |
Clay JM, Vedejs E. Hydroboration with pyridine borane at room temperature. Journal of the American Chemical Society. 127: 5766-7. PMID 15839656 DOI: 10.1021/Ja043743J |
0.784 |
|
| 2004 |
Kim M, Vedejs E. A synthetic approach toward the proposed tetracyclic aziridinomitosene derived from FK317. The Journal of Organic Chemistry. 69: 7262-5. PMID 15471479 DOI: 10.1021/Jo040211C |
0.69 |
|
| 2004 |
Kim M, Vedejs E. A reinvestigation of 4-hydroxyindole-6-carboxylate synthesis from pyrrole-2-carboxaldehyde: a facile synthesis of indoles and indolizines. The Journal of Organic Chemistry. 69: 6945-8. PMID 15387633 DOI: 10.1021/Jo040191E |
0.654 |
|
| 2004 |
MacKay JA, Vedejs E. Enantioselective acylation using a second-generation P-aryl-2-phosphabicyclo[3.3.0]octane catalyst. The Journal of Organic Chemistry. 69: 6934-7. PMID 15387630 DOI: 10.1021/Jo049112P |
0.635 |
|
| 2004 |
Vedejs E. Studies in heteroelement-based synthesis. The Journal of Organic Chemistry. 69: 5159-67. PMID 15287757 DOI: 10.1021/Jo049360L |
0.363 |
|
| 2004 |
Shapland P, Vedejs E. Intramolecular hydroboration of unsaturated phosphine boranes. The Journal of Organic Chemistry. 69: 4094-100. PMID 15176834 DOI: 10.1021/Jo040125C |
0.386 |
|
| 2004 |
Vedejs E, Little JD. Synthesis of the aziridinomitosene skeleton by intramolecular Michael addition of alpha-lithioaziridines: an aromatic route featuring deuterium as a removable blocking group. The Journal of Organic Chemistry. 69: 1794-9. PMID 15058920 DOI: 10.1021/jo030223i |
0.743 |
|
| 2004 |
Vedejs E, Little JD, Seaney LM. Synthesis of the aziridinomitosene skeleton by intramolecular Michael addition: alpha-lithioaziridines and nonaromatic substrates. The Journal of Organic Chemistry. 69: 1788-93. PMID 15058919 DOI: 10.1021/Jo030224A |
0.753 |
|
| 2004 |
Vedejs E, Daugulis O, Tuttle N. Desymmetrization of meso-hydrobenzoin using chiral, nucleophilic phosphine catalysts. The Journal of Organic Chemistry. 69: 1389-92. PMID 14961701 DOI: 10.1021/jo030279c |
0.613 |
|
| 2004 |
Zajac MA, Vedejs E. A synthesis of the diazonamide heteroaromatic biaryl macrocycle/hemiaminal core. Organic Letters. 6: 237-40. PMID 14723537 DOI: 10.1021/Ol036179A |
0.802 |
|
| 2004 |
Klapars A, Vedejs E. Activation of pyridinium salts for electrophilic acylation: A method for conversion of pyridines into 3-acylpyridines Khimiya Geterotsiklicheskikh Soedinenii. 887-894. DOI: 10.1023/B:COHC.0000040772.13427.0b |
0.66 |
|
| 2004 |
Klapars A, Vedejs E. Activation of pyridinium salts for electrophilic acylation: A method for conversion of pyridines into 3-acylpyridines Khimiya Geterotsiklicheskikh Soedinenii. 887-894. DOI: 10.1023/B:Cohc.0000040772.13427.0B |
0.68 |
|
| 2003 |
Vedejs E, Naidu BN, Klapars A, Warner DL, Li VS, Na Y, Kohn H. Synthetic enantiopure aziridinomitosenes: preparation, reactivity, and DNA alkylation studies. Journal of the American Chemical Society. 125: 15796-806. PMID 14677970 DOI: 10.1021/Ja030452M |
0.799 |
|
| 2003 |
Shaw SA, Aleman P, Vedejs E. Development of chiral nucleophilic pyridine catalysts: applications in asymmetric quaternary carbon synthesis. Journal of the American Chemical Society. 125: 13368-9. PMID 14583027 DOI: 10.1021/Ja037223K |
0.385 |
|
| 2003 |
Smulik JA, Vedejs E. Improved reagent for electrophilic amination of stabilized carbanions. Organic Letters. 5: 4187-90. PMID 14572281 DOI: 10.1021/Ol035629W |
0.791 |
|
| 2003 |
Scheideman M, Shapland P, Vedejs E. A mechanistic alternative for the intramolecular hydroboration of homoallylic amine and phosphine borane complexes. Journal of the American Chemical Society. 125: 10502-3. PMID 12940716 DOI: 10.1021/Ja034655M |
0.782 |
|
| 2003 |
Vedejs E, Daugulis O, Harper LA, MacKay JA, Powell DR. A comparison of monocyclic and bicyclic phospholanes as acyl-transfer catalysts. The Journal of Organic Chemistry. 68: 5020-7. PMID 12816454 DOI: 10.1021/jo030007+ |
0.769 |
|
| 2003 |
Vedejs E, Daugulis O. A highly enantioselective phosphabicyclooctane catalyst for the kinetic resolution of benzylic alcohols. Journal of the American Chemical Society. 125: 4166-73. PMID 12670239 DOI: 10.1021/Ja021224F |
0.645 |
|
| 2003 |
Vedejs E, Prasad ASB, Kendall JT, Russel JS. The stereochemistry of aziridine borane lithiation: Diastereoselectivity and enantioselectivity Tetrahedron. 59: 9849-9856. DOI: 10.1016/j.tet.2003.09.035 |
0.336 |
|
| 2003 |
Vedejs E, Larsen S. Hydroxylation of Enolates with Oxodiperoxymolybdenum(Pyridine)(Hexamethylphosphoric Triamide), MoO5·Py·HMPA(MoOPH): 3‐Hydroxy‐1,7,7‐Trimethylbicyclo[2.2.1]Heptan‐2‐one Organic Syntheses. 127-127. DOI: 10.1002/0471264180.Os064.20 |
0.346 |
|
| 2002 |
Vedejs E, Little J. Aziridinomitosenes by anionic cyclization: deuterium as a removable blocking group. Journal of the American Chemical Society. 124: 748-9. PMID 11817939 DOI: 10.1021/ja0120835 |
0.731 |
|
| 2001 |
Vedejs E, Klapars A, Warner DL, Weiss AH. Reductive deprotection of N-tritylaziridines. The Journal of Organic Chemistry. 66: 7542-6. PMID 11681978 DOI: 10.1021/jo0106243 |
0.763 |
|
| 2001 |
Vedejs E, Kongkittingam C. A total synthesis of (-)-hemiasterlin using N-Bts methodology. The Journal of Organic Chemistry. 66: 7355-64. PMID 11681948 DOI: 10.1021/Jo0104882 |
0.8 |
|
| 2001 |
Vedejs E, Zajac MA. Synthesis of the diazonamide A macrocyclic core via a Dieckmann-type cyclization. Organic Letters. 3: 2451-4. PMID 11483032 DOI: 10.1021/Ol016097R |
0.801 |
|
| 2001 |
Vedejs E, MacKay JA. Kinetic resolution of allylic alcohols using a chiral phosphine catalyst. Organic Letters. 3: 535-6. PMID 11178818 DOI: 10.1021/Ol006923G |
0.606 |
|
| 2001 |
Vedejs E, Daugulis O, MacKay JA, Rozners E. Enantioselective acyl transfer using chiral phosphine catalysts Synlett. 1499-1505. DOI: 10.1055/S-2001-17436 |
0.711 |
|
| 2000 |
Vedejs E, Duncan SM. A synthesis of C(16),C(18)-bis-epi-cytochalasin D via Reformatsky cyclization. The Journal of Organic Chemistry. 65: 6073-81. PMID 10987942 DOI: 10.1021/jo000533q |
0.34 |
|
| 2000 |
Vedejs E, Piotrowski DW, Tucci FC. Oxazolium-derived azomethine ylides. External oxazole activation and internal dipole trapping in the synthesis of an aziridinomitosene. The Journal of Organic Chemistry. 65: 5498-505. PMID 10970287 DOI: 10.1021/Jo0001277 |
0.43 |
|
| 2000 |
Vedejs E, Barda DA. Progress toward synthesis of diazonamide A. Preparation of a 3-(oxazol-5-yl)-4-trifluoromethyl-sulfonyloxyindole and its use in biaryl coupling reactions. Organic Letters. 2: 1033-5. PMID 10804547 DOI: 10.1021/Ol005548P |
0.435 |
|
| 2000 |
Vedejs E, Wang J. A tyrosine-derived benzofuranone related to diazonamide A. Organic Letters. 2: 1031-2. PMID 10804546 DOI: 10.1021/Ol005547X |
0.363 |
|
| 2000 |
Vedejs E, Donde Y. Crystallization-induced asymmetric transformation of a tertiary phosphine The Journal of Organic Chemistry. 65: 2337-43. PMID 10789444 DOI: 10.1021/Jo991493X |
0.37 |
|
| 2000 |
Vedejs E, Kongkittingam C. Solution-phase synthesis of a hindered N-methylated tetrapeptide using Bts-protected amino acid chlorides: efficient coupling and methylation steps allow purification by extraction. The Journal of Organic Chemistry. 65: 2309-18. PMID 10789440 DOI: 10.1021/Jo9914115 |
0.791 |
|
| 2000 |
Vedejs E, Klapars A, Naidu BN, Piotrowski DW, Tucci FC. Enantiocontrolled synthesis of (1S,2S)-6-desmethyl- (methylaziridino)mitosene [8] Journal of the American Chemical Society. 122: 5401-5402. DOI: 10.1021/ja994504c |
0.639 |
|
| 2000 |
Vedejs E, Kruger AW, Lee N, Sakata ST, Stec M, Suna E. Enantioselective enolate protonation with chiral anilines: Scope, structural requirements, and mechanistic implications Journal of the American Chemical Society. 122: 4602-4607. DOI: 10.1021/ja994437m |
0.625 |
|
| 1999 |
Vedejs E, Trapencieris P, Suna E. Substituted Isoquinolines by Noyori Transfer Hydrogenation: Enantioselective Synthesis of Chiral Diamines Containing an Aniline Subunit. The Journal of Organic Chemistry. 64: 6724-6729. PMID 11674678 DOI: 10.1021/Jo990594S |
0.404 |
|
| 1999 |
Vedejs E, Kruger AW. Diastereoselective Osmylation and Hydroboration of beta,gamma-Unsaturated N,N-Diisopropylamides and Acid-Catalyzed Conversion to delta-Lactones. The Journal of Organic Chemistry. 64: 4790-4797. PMID 11674553 DOI: 10.1021/Jo990119U |
0.401 |
|
| 1999 |
Vedejs E, Kruger AW, Suna E. Enantioselective enolate protonation: Matching chiral aniline and substrate acidity Journal of Organic Chemistry. 64: 7863-7870. DOI: 10.1021/Jo990897M |
0.382 |
|
| 1999 |
Vedejs E, Daugulis O. 2-Aryl-4,4,8-trimethyl-2-phosphabicyclo[3.3.0]octanes: Reactive chiral phosphine catalysts for enantioselective acylation Journal of the American Chemical Society. 121: 5813-5814. DOI: 10.1021/Ja990133O |
0.632 |
|
| 1998 |
Vedejs E, Daugulis O, Diver ST, Powell DR. Generation of the 1,3-Phosphasilolene Skeleton from Ortho-Silylated Biarylphosphonates Journal of Organic Chemistry. 63: 2338-2341. DOI: 10.1021/Jo972229B |
0.563 |
|
| 1998 |
Vedejs E, Kruger AW. Catalytic Asymmetric Protonation of Amide Enolates: Optimization of Kinetic Acidity in the Catalytic Cycle Journal of Organic Chemistry. 63: 2792-2793. DOI: 10.1021/Jo972147N |
0.313 |
|
| 1998 |
Vedejs E, Galante RJ, Goekjian PG. A thio-Diels-Alder route to the azocine ring system. Total synthesis of (±)-otonecine Journal of the American Chemical Society. 120: 3613-3622. DOI: 10.1021/Ja973464E |
0.42 |
|
| 1997 |
Vedejs E, Monahan SD. Competing Pathways in the Azomethine Ylide Route to Indoloquinones: An Improved Procedure for the Generation of a Transient 4-Oxazoline from the Oxazolium Salt Journal of Organic Chemistry. 62: 4763-4769. DOI: 10.1021/Jo9702195 |
0.372 |
|
| 1996 |
Vedejs E, Daugulis O, Diver ST. Enantioselective Acylations Catalyzed by Chiral Phosphines. The Journal of Organic Chemistry. 61: 430-431. PMID 11666951 DOI: 10.1021/Jo951661V |
0.752 |
|
| 1996 |
Vedejs E, Daugulis O. Dual activation in the esterification of hindered alcohols with anhydrides using MgBr2 and a tertiary amine Journal of Organic Chemistry. 61: 5702-5703. DOI: 10.1021/Jo9609485 |
0.575 |
|
| 1996 |
Vedejs E, Lin S, Klapars A, Wang J. Heteroarene-2-sulfonyl chlorides (BtsCl; ThsCl): Reagents for nitrogen protection of >99% racemization-free phenylglycine activation with SOCl2 Journal of the American Chemical Society. 118: 9796-9797. DOI: 10.1021/Ja961485N |
0.686 |
|
| 1996 |
Vedejs E, Chen X. Kinetic resolution of secondary alcohols. Enantioselective acylation mediated by a chiral (dimethylamino)pyridine derivative Journal of the American Chemical Society. 118: 1809-1810. DOI: 10.1021/Ja953631F |
0.334 |
|
| 1994 |
Vedejs E, Lin S. Deprotection of arenesulfonamides with samarium iodide Journal of Organic Chemistry. 59: 1602-1603. DOI: 10.1021/Jo00086A005 |
0.329 |
|
| 1993 |
Vedejs E, Duncan SM, Haight AR. An internally activated tin hydride with enhanced reducing ability Journal of Organic Chemistry. 58: 3046-3050. DOI: 10.1021/Jo00063A024 |
0.352 |
|
| 1993 |
Vedejs E, Peterson MJ. A bridged tetrahydrophosphole ylide derived from 9-phenylphosphabicyclo[4.2.1]nonane: A reagent for E-selective Wittig reactions Journal of Organic Chemistry. 58: 1985-1986. DOI: 10.1021/Jo00060A001 |
0.323 |
|
| 1993 |
Vedejs E, Piotrowski DW. Oxazole activation for azomethine ylide trapping: Singly and doubly tethered substrates Journal of Organic Chemistry. 58: 1341-1348. DOI: 10.1021/Jo00058A010 |
0.367 |
|
| 1993 |
Vedejs E, Diver ST. Tributylphosphine: a remarkable acylation catalyst Journal of the American Chemical Society. 115: 3358-3359. DOI: 10.1021/ja00061a056 |
0.583 |
|
| 1992 |
Vedejs E, Sano H. Synthesis of N-methoxy and N-H aziridines from alkenes Tetrahedron Letters. 33: 3261-3264. DOI: 10.1016/S0040-4039(00)92062-8 |
0.332 |
|
| 1990 |
Vedejs E, Reid JG, Rodgers JD, Wittenberger SJ. Synthesis of cytochalasins: The route to sulfur-bridged [11] cytochalasans Journal of the American Chemical Society. 112: 4351-4357. DOI: 10.1021/Ja00167A036 |
0.728 |
|
| 1990 |
Vedejs E, Wittenberger SJ. The total syntheses of dl-zygosporin E and dl-C18-desmethylcytochalasin D Journal of the American Chemical Society. 112: 4357-4364. |
0.656 |
|
| 1989 |
Vedejs E, Dax SL. Indoloquinones from azomethine ylides via the 4-oxazoline route Tetrahedron Letters. 30: 2627-2630. DOI: 10.1016/S0040-4039(00)99082-8 |
0.381 |
|
| 1988 |
Vedejs E, Rodgers JD, Wittenberger SJ. A sulfur-mediated total synthesis of zygosporin E Journal of the American Chemical Society. 110: 4822-4823. DOI: 10.1021/Ja00222A047 |
0.702 |
|
| 1988 |
Vedejs E, Ahmad S. Synthesis of the 11-membered cytochalasin ring system by modified reformatsky cyclization Tetrahedron Letters. 29: 2291-2294. DOI: 10.1016/S0040-4039(00)86040-2 |
0.394 |
|
| 1988 |
Vedejs E, Rodgers JD, Wittenberger SJ. A mild procedure for synthesis of the cytochalasin isoindolone; Allyl selenides from allyl silanes and PhSeSe+(CH3)Ph BF4 - Tetrahedron Letters. 29: 2287-2290. DOI: 10.1016/S0040-4039(00)86039-6 |
0.688 |
|
| 1988 |
Vedejs E, Stults JS. Synthesis of azocine derivatives from thioaldehyde diels-alder adducts Journal of Organic Chemistry. 53: 2226-2232. |
0.315 |
|
| 1987 |
Vedejs E, Ahmad S, Larsen SD, Westwood S. Synthesis of monocrotaline by nucleophilic macrolactonization Journal of Organic Chemistry. 52: 3937-3938. DOI: 10.1021/Jo00226A045 |
0.421 |
|
| 1987 |
Vedejs E, Marth C. DBP ylides: Wittig reagents for synthesis of E-alkenes from aldehydes Tetrahedron Letters. 28: 3445-3448. DOI: 10.1016/S0040-4039(00)96322-6 |
0.387 |
|
| 1987 |
Vedejs E. Dihydrothiopyrans in complex total synthesis Chemistry of Heterocyclic Compounds. 23: 1269-1283. DOI: 10.1007/Bf00472246 |
0.333 |
|
| 1987 |
Vedejs E, Dent WH, Gapinski DM, McClure CK. Local conformer effects in unsaturated lactones Journal of the American Chemical Society. 109: 5437-5446. |
0.444 |
|
| 1986 |
Vedejs E, West FG. Ylides by the desilylation of .alpha.-silyl onium salts Chemical Reviews. 86: 941-955. DOI: 10.1021/Cr00075A014 |
0.524 |
|
| 1986 |
Vedejs E, McClure CK. Hyperconjugative effects of allylic substituents are not important in osmylations Journal of the American Chemical Society. 108: 1094-1096. |
0.53 |
|
| 1986 |
Vedejs E, West FG. Ylides by the desilylation of α-silyl onium salts Chemical Reviews. 86: 941-955. |
0.476 |
|
| 1986 |
Vedejs E, Eberlein TH, Mazur DJ, McClure CK, Perry DA, Ruggeri R, Schwartz E, Stults JS, Varie DL, Wilde RG, Wittenberger S. Thioaldehyde Diels-Alder reactions Journal of Organic Chemistry. 51: 1556-1562. |
0.743 |
|
| 1985 |
Vedejs E, Larsen S, West FG. Nonstabilized imidate ylides by the desilylation method: A route to the pyrrolizidine alkaloids retronecine and indicine Journal of Organic Chemistry. 50: 2170-2174. DOI: 10.1002/Chin.198547317 |
0.551 |
|
| 1983 |
Vedejs E, West FE. Thioimidate methylides by the desilylation method: An improved synthesis of pyrrolines and pyrroles Journal of Organic Chemistry. 48: 4773-4774. DOI: 10.1021/Jo00172A064 |
0.335 |
|
| 1982 |
Vedejs E, Campbell JB, Gadwood RC, Rodgers JD, Spear KL, Watanabe Y. Synthesis of the cytochalasin D isoindolone unit: Solutions to the problem of regiochemistry in N-benzoylpyrrolinone Diels-Alder reactions Journal of Organic Chemistry. 47: 1534-1546. DOI: 10.1021/Jo00347A034 |
0.684 |
|
| 1982 |
Vedejs E, Arnost MJ, Eustache JM, Krafft GA. Model study for synthesis of the cytochalasin D cycloundecanone ring system Journal of Organic Chemistry. 47: 4384-4386. |
0.603 |
|
| 1981 |
Vedejs E, Gapinski DM, Hagen JP. Studies in macrolide synthesis: Sulfur-bridged lactones from ring expansion via intramolecular S-alkylation Journal of Organic Chemistry. 46: 5451-5452. DOI: 10.1021/Jo00339A053 |
0.394 |
|
| 1981 |
Vedejs E, Mastalerz H, Meier GP, Powell DW. Thiol esters from sulfoxides via rearrangement of sulfoxide phosphines to sulfide phosphine oxides Journal of Organic Chemistry. 46: 5253-5254. DOI: 10.1021/Jo00338A052 |
0.307 |
|
| 1981 |
Vedejs E, Meier GP, Snoble KAJ. Low-temperature characterization of the intermediates in the Wittig reaction Journal of the American Chemical Society. 103: 2823-2831. DOI: 10.1021/Ja00400A055 |
0.309 |
|
| 1980 |
Vedejs E. The 1979 nobel prize for chemistry. Science (New York, N.Y.). 207: 42-4. PMID 17730797 DOI: 10.1126/Science.207.4426.42 |
0.374 |
|
| 1980 |
Vedejs E, Martinez GR. Stereospecific synthesis of retronecine by imidate methylide cycloaddition [42] Journal of the American Chemical Society. 102: 7993-7994. |
0.306 |
|
| 1979 |
Vedejs E, Meier GP. lactam synthesis by intramolecular ene insertion of acylazocarboxylates Tetrahedron Letters. 20: 4185-4188. DOI: 10.1016/S0040-4039(01)86539-4 |
0.394 |
|
| 1979 |
Muxfeldt H, Haas G, Hardtmann G, Kathawala F, Mooberry JB, Vedejs E. Tetracyclines. 9. Total synthesis of dl-terramycin Journal of the American Chemical Society. 101: 689-701. DOI: 10.1002/Chin.197919375 |
0.66 |
|
| 1978 |
Vedejs E, Gadwood RC. An approach to cytochalasins: Diels-Alder addition of alpha,beta-unsaturated imides. The Journal of Organic Chemistry. 43: 376-8. PMID 621600 DOI: 10.1021/Jo00396A058 |
0.624 |
|
| 1978 |
Vedejs E, Arco MJ, Powell DW, Renga JM, Singer SP. Ring expansion of 2-vinyl derivatives of thiane, N-benzylpiperidine, and thiepane by [2,3] sigmatropic shift Journal of Organic Chemistry. 43: 4831-4837. DOI: 10.1021/Jo00419A040 |
0.341 |
|
| 1978 |
Vedejs E, Singer SP. Ramberg-Backlund sulfur extrusion from 2-carboethoxy sulfones Journal of Organic Chemistry. 43: 4884-4885. DOI: 10.1021/Jo00419A025 |
0.308 |
|
| 1978 |
Vedejs E, Mullins MJ, Renga JM, Singer SP. Repeatable ring expansions using allyl triflate Tetrahedron Letters. 19: 519-522. DOI: 10.1016/S0040-4039(01)85321-1 |
0.315 |
|
| 1977 |
Vedejs E, Stolle WT. Reductive alkylation of aldehyde tosylhydrazones with organolithium reagents Tetrahedron Letters. 18: 135-138. DOI: 10.1016/S0040-4039(01)92569-9 |
0.452 |
|
| 1976 |
Vedejs E, Engler DA. Efficient conversion of sulfides into ester-stabilized ylids; alkene synthesis via ylid fragmentation Tetrahedron Letters. 17: 3487-3490. DOI: 10.1016/S0040-4039(00)71337-2 |
0.385 |
|
| 1975 |
Vedejs E, Wilber WR. A facile bis-norcaradiene rearrangement Tetrahedron Letters. 16: 2679-2682. DOI: 10.1016/S0040-4039(00)75212-9 |
0.333 |
|
| 1975 |
Vedejs E, Bershas J. A new route to stabilized ylides: A one-pot polyene synthesis Tetrahedron Letters. 16: 1359-1362. DOI: 10.1016/S0040-4039(00)72142-3 |
0.341 |
|
| 1974 |
Vedejs E, Weeks P. Pd°-catalyzed mercury extrusion: Stereoselective conversion of bis(propenyl)-mercury into 2,4-hexadiene Tetrahedron Letters. 15: 3207-3210. DOI: 10.1016/S0040-4039(01)91863-5 |
0.398 |
|
| 1973 |
Vedejs E, Bershas JP, Fuchs PL. .gamma.-Substitution of allyl ylides in the Wittig reaction The Journal of Organic Chemistry. 38: 3625-3627. DOI: 10.1021/Jo00960A044 |
0.665 |
|
| 1973 |
Vedejs E, Snoble KAJ, Fuchs PL. Phosphorus betaines derived from cycloheptene and cyclooctene oxides. Inversion of cyclooctene The Journal of Organic Chemistry. 38: 1178-1183. DOI: 10.1021/Jo00946A024 |
0.6 |
|
| 1973 |
Vedejs E, Fuchs PL. Inversion of acyclic olefins by the phosphorus betaine method. Scope and limitations Journal of the American Chemical Society. 95: 822-825. DOI: 10.1021/Ja00784A032 |
0.608 |
|
| 1973 |
VEDEJS E, SNOBLE KAJ, FUCHS PL. ChemInform Abstract: PHOSPHORBETAINE AUS CYCLOHEPTEN- UND CYCLOOCTENOXIDEN, INVERSION VON CYCLOOCTENEN Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197325388 |
0.591 |
|
| 1972 |
Vedejs E, Salomon MF. Preparation, stereochemistry, and rearrangement of mercurials in the norbornenyl-nortricyclyl system The Journal of Organic Chemistry. 37: 2075-2079. DOI: 10.1021/Jo00978A005 |
0.367 |
|
| 1971 |
Vedejs E, Fuchs PL. Improved aldehyde synthesis from 1,3-dithianes The Journal of Organic Chemistry. 36: 366-367. DOI: 10.1021/Jo00801A033 |
0.673 |
|
| 1971 |
Vedejs E, Fuchs PL. Olefin inversion by the phosphorus betaine method Journal of the American Chemical Society. 93: 4070-4072. DOI: 10.1021/Ja00745A054 |
0.596 |
|
| 1968 |
Muxfeldt H, Hardtmann G, Kathawala F, Vedejs E, Mooberry JB. Tetracyclines. VII. Total synthesis of dl-terramycin. Journal of the American Chemical Society. 90: 6534-6. PMID 5682455 DOI: 10.1021/Ja01025A063 |
0.659 |
|
| 1968 |
Corey EJ, Andersen NH, Carlson RM, Paust J, Vedejs E, Vlattas I, Winter RE. Total synthesis of prostaglandins. Synthesis of the pure dl-E1, -F1-alpha-F1-beta, -A1, and -B1 hormones. Journal of the American Chemical Society. 90: 3245-7. PMID 5649181 DOI: 10.1021/Ja01014A053 |
0.718 |
|
| 1968 |
Vedejs E. The reaction of benzyne with cyclooctatetraene Tetrahedron Letters. 9: 2633-2638. DOI: 10.1016/S0040-4039(00)89661-6 |
0.32 |
|
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