Year |
Citation |
Score |
2023 |
Pounder A, Neufeld E, Myler P, Tam W. Transition-metal-catalyzed domino reactions of strained bicyclic alkenes. Beilstein Journal of Organic Chemistry. 19: 487-540. PMID 37153643 DOI: 10.3762/bjoc.19.38 |
0.326 |
|
2022 |
Ho A, Pounder A, Valluru K, Chen LD, Tam W. Iridium-catalyzed hydroacylation reactions of C1-substituted oxabenzonorbornadienes with salicylaldehyde: an experimental and computational study. Beilstein Journal of Organic Chemistry. 18: 251-261. PMID 35330776 DOI: 10.3762/bjoc.18.30 |
0.379 |
|
2021 |
Pounder A, Tam W. Iron-catalyzed domino coupling reactions of π-systems. Beilstein Journal of Organic Chemistry. 17: 2848-2893. PMID 34956407 DOI: 10.3762/bjoc.17.196 |
0.367 |
|
2021 |
Pounder A, Chen LD, Tam W. Ruthenium-Catalyzed [2 + 2] versus Homo Diels-Alder [2 + 2 + 2] Cycloadditions of Norbornadiene and Disubstituted Alkynes: A DFT Study. Acs Omega. 6: 900-911. PMID 33458541 DOI: 10.1021/acsomega.0c05499 |
0.332 |
|
2021 |
Pounder A, Ho A, Macleod M, Tam W. Chemistry of Unsymmetrical C1-Substituted Oxabenzonorbornadienes. Current Organic Synthesis. PMID 33402089 DOI: 10.2174/1570179417666210105121115 |
0.352 |
|
2020 |
Koh S, Pounder A, Brown E, Tam W. Intramolecular Palladium-Catalyzed Ring Opening of Oxabenzonorbornadienes with C-Tethered Aryl Halides. Organic Letters. PMID 32294386 DOI: 10.1021/Acs.Orglett.0C00900 |
0.57 |
|
2020 |
Koh S, Pounder A, Brown E, Tam W. Intramolecular Nickel‐Catalyzed Ring‐Opening Reactions of Oxabenzonorbornadienes with C1‐Tethered Aryl Halides: An Improvement of Method European Journal of Organic Chemistry. 2020: 4558-4562. DOI: 10.1002/Ejoc.202000672 |
0.498 |
|
2019 |
Petko D, Koh S, Tam W. Transition Metal-Catalyzed Reactions of Alkynyl Halides. Current Organic Synthesis. 16: 546-582. PMID 31984930 DOI: 10.2174/1570179416666190329200616 |
0.393 |
|
2019 |
Boutin R, Koh S, Tam W. Recent Advances in Transition Metal-Catalyzed Reactions of Oxabenzonorbornadiene. Current Organic Synthesis. 16: 460-484. PMID 31984926 DOI: 10.2174/1570179416666181122094643 |
0.446 |
|
2019 |
Petko D, Stratton M, Koh S, Tam W. Cationic Ruthenium-Catalyzed Bis-Homo-Diels-Alder Cycloaddition. Current Organic Synthesis. 16: 787-792. PMID 31984894 DOI: 10.2174/1570179416666190401204448 |
0.422 |
|
2019 |
Hill J, Tam W. Palladium/Lewis Acid Cocatalyzed Ring-Opening Reactions of Unsymmetrical Oxabenzonobornadienes with Oximes. The Journal of Organic Chemistry. PMID 31192590 DOI: 10.1021/Acs.Joc.9B01094 |
0.535 |
|
2019 |
Tait K, Koh S, Blanchard N, Tam W. Ruthenium-catalyzed ring-opening reaction of a 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with amines — an unexpected mode of ring-opening Canadian Journal of Chemistry. 97: 310-316. DOI: 10.1139/Cjc-2018-0444 |
0.561 |
|
2019 |
Petko D, Pounder A, Tam W. Ruthenium-Catalyzed [2+2+2] Bis-Homo-Diels–Alder Cycloadditions of 1,5-Cyclooctadiene with Alkynyl Phosphonates Synthesis. 51: 4271-4278. DOI: 10.1055/S-0039-1690612 |
0.52 |
|
2019 |
Wicks C, Koh S, Pounder A, Carlson E, Tam W. Acid-catalyzed intramolecular ring-opening reactions of cyclopropanated oxabenzonorbornadienes with alcohol nucleophiles Tetrahedron Letters. 60: 151228. DOI: 10.1016/J.Tetlet.2019.151228 |
0.486 |
|
2019 |
Hill J, Wicks C, Pounder A, Tam W. Iridium-catalyzed ring-opening reactions of unsymmetrical oxabenzonorbornadienes with water and alcohol nucleophiles Tetrahedron Letters. 60: 150990. DOI: 10.1016/J.Tetlet.2019.150990 |
0.533 |
|
2018 |
Tait K, Tam W. Transition Metal-Catalyzed Reactions of 3-Aza-2-oxabicyclo[2.2.1]hept-5-enes Current Organic Synthesis. 15: 762-780. DOI: 10.2174/1570179415666180524112250 |
0.396 |
|
2018 |
Petko D, Stratton M, Tam W. Ruthenium-catalyzed Bis-Homo-Diels-Alder reaction: searching for commercially available catalysts and expanding the scope of reaction Canadian Journal of Chemistry. 96: 1115-1121. DOI: 10.1139/Cjc-2018-0117 |
0.536 |
|
2018 |
Carlson E, Boutin R, Tam W. Type 3 ring opening reaction of cyclopropanated oxabenzonorbornadienes with alcohol nucleophiles Tetrahedron. 74: 5510-5518. DOI: 10.1016/J.Tet.2018.03.063 |
0.504 |
|
2017 |
Tait K, Horvath A, Blanchard N, Tam W. Acid-catalyzed ring-opening reactions of a cyclopropanated 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with alcohols. Beilstein Journal of Organic Chemistry. 13: 2888-2894. PMID 29564016 DOI: 10.3762/Bjoc.13.281 |
0.539 |
|
2017 |
Lough AJ, Tait K, Horvath A, Tam W. tert-Butyl N-[(1R*,2R*,4R*,5S*)-rel-4-tert-butoxybicyclo[3.1.0]hex-2-yl]-N-hydroxycarbamate Iucrdata. 2. DOI: 10.1107/S2414314617014195 |
0.325 |
|
2017 |
Lough AJ, Tait K, Tam W. tert-Butyl (3-oxocyclopentyl)carbamate Iucrdata. 2. DOI: 10.1107/S2414314617014183 |
0.349 |
|
2017 |
Lough AJ, Carlson E, Tam W. (5R,6R)-rel-9-tert-Butyl-trans-5,6-dimethoxy-6,7-dihydro-5H-benzocycloheptene Iucrdata. 2. DOI: 10.1107/S2414314617014171 |
0.315 |
|
2016 |
Tait K, Alrifai O, Boutin R, Haner J, Tam W. Palladium-catalyzed ring-opening reactions of cyclopropanated 7-oxabenzonorbornadiene with alcohols. Beilstein Journal of Organic Chemistry. 12: 2189-2196. PMID 27829926 DOI: 10.3762/Bjoc.12.209 |
0.547 |
|
2016 |
Carlson E, Tam W. Type 1 Ring-Opening Reactions of Cyclopropanated 7-Azabenzonorbornadienes with Organocuprates. Organic Letters. PMID 27055059 DOI: 10.1021/Acs.Orglett.6B00757 |
0.544 |
|
2016 |
Edmunds M, Raheem MA, Boutin R, Tait K, Tam W. Regioselective palladium-catalyzed ring-opening reactions of C1-substituted oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates. Beilstein Journal of Organic Chemistry. 12: 239-44. PMID 26977182 DOI: 10.3762/Bjoc.12.25 |
0.58 |
|
2016 |
Carlson E, Duret G, Blanchard N, Tam W. Synthesis of cyclopropanated [2.2.1] heterobicycloalkenes: An improved procedure Synthetic Communications. 46: 55-62. DOI: 10.1080/00397911.2015.1118124 |
0.478 |
|
2016 |
Carlson E, Hong D, Tam W. Type 2 Ring-Opening Reactions of Cyclopropanated 7-Oxabenzonorbornadienes with Carboxylic Acid Nucleophiles Synthesis (Germany). DOI: 10.1055/S-0035-1560565 |
0.513 |
|
2015 |
Edmunds M, Menard ML, Tam W. Study on the regioselectivity of rhodium-catalyzed ring opening reactions of C1-substituted 7-oxabenzonorbornadienes with boronic acids Synthetic Communications. 45: 468-476. DOI: 10.1080/00397911.2014.965330 |
0.538 |
|
2014 |
Goodreid J, Villeneuve K, Carlson E, Tam W. Ruthenium-catalyzed asymmetric [2 + 2] cycloadditions between chiral acyl camphorsultam-substituted alkynes and bicyclic alkenes. The Journal of Organic Chemistry. 79: 10002-12. PMID 25303019 DOI: 10.1021/Jo501594G |
0.542 |
|
2014 |
Nagireddy JR, Tranmer GK, Carlson E, Tam W. N-O Cleavage reactions of heterobicycloalkene-fused 2-isoxazolines. Beilstein Journal of Organic Chemistry. 10: 2200-5. PMID 25246978 DOI: 10.3762/Bjoc.10.227 |
0.447 |
|
2014 |
Lough AJ, Raheem MA, Tam W. cis-2-(4-Meth-oxy-phen-yl)-4-methyl-1,2-di-hydro-naphthalen-1-ol. Acta Crystallographica. Section E, Structure Reports Online. 70: o546. PMID 24860354 DOI: 10.1107/S1600536814007739 |
0.341 |
|
2014 |
Lough AJ, Nagireddy JR, Tam W. 1-(3-Hy-droxy-5,8-dimeth-oxy-4-methyl-1,2,3,4-tetra-hydro-1,4-ep-oxy-naphthalen-2-yl)ethan-1-one. Acta Crystallographica. Section E, Structure Reports Online. 70: o545. PMID 24860353 DOI: 10.1107/S1600536814007764 |
0.335 |
|
2014 |
Lough AJ, Nagireddy JR, Tam W. 5,8-Dimeth-oxy-3,9-dimethyl-3a,4,9,9a-tetra-hydro-4,9-ep-oxy-naphtho-[2,3-d]isoxazole. Acta Crystallographica. Section E, Structure Reports Online. 70: o544. PMID 24860352 DOI: 10.1107/S1600536814007752 |
0.335 |
|
2014 |
Lough AJ, Nagireddy JR, Tam W. (3-Methyl-3a,4,7,7a-tetra-hydro-5H-4,7-methano-isoxazolo[4,5-d][1,2]oxazin-5-yl)(phen-yl)methanone. Acta Crystallographica. Section E, Structure Reports Online. 70: o543. PMID 24860351 DOI: 10.1107/S1600536814007740 |
0.319 |
|
2014 |
Carlson E, Haner J, McKee M, Tam W. Type 1 ring-opening reactions of cyclopropanated 7-oxabenzonorbornadienes with organocuprates. Organic Letters. 16: 1776-9. PMID 24617505 DOI: 10.1021/ol5004737 |
0.445 |
|
2014 |
Nagireddy JR, Carlson E, Tam W. 1,3-Dipolar cycloaddition of nitrile oxides with C1-substituted 7-oxabenzonorbornadienes Canadian Journal of Chemistry. 92: 1053-1058. DOI: 10.1139/Cjc-2014-0274 |
0.495 |
|
2014 |
Raheem MA, Edmunds M, Tam W. Regioselective palladium-catalyzed ring-opening reactions of C 1-substituted oxabenzonorbornadienes Canadian Journal of Chemistry. 92: 888-895. DOI: 10.1139/cjc-2014-0217 |
0.482 |
|
2014 |
Nagireddy JR, Carlson E, Tam W. 1,3-Dipolar cycloadditions of nitrile oxides with 7-oxa-and 7-azabenzonorbornadienes Canadian Journal of Chemistry. 92: 635-639. DOI: 10.1139/Cjc-2014-0140 |
0.405 |
|
2014 |
McKee M, Haner J, Carlson E, Tam W. Synthesis of Cyclopropanated 7-Oxabenzonorbornadienes Synthesis (Germany). 46: 1518-1524. DOI: 10.1055/S-0035-1561600 |
0.45 |
|
2014 |
Tigchelaar A, Haner J, Carlson E, Tam W. Type 2 Ring-Opening Reactions of Cyclopropanated 7-Oxabenzonorbornadienes under Acid Catalysis Synlett. 25: 2355-2359. DOI: 10.1055/S-0034-1378581 |
0.481 |
|
2014 |
Tsui GC, Villeneuve K, Carlson E, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions between norbornene and propargylic alcohols or their derivatives Organometallics. 33: 3847-3856. DOI: 10.1021/Om500563H |
0.744 |
|
2013 |
Jack K, Tam W. Ruthenium-catalyzed dimerization of 7-oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates. The Journal of Organic Chemistry. 78: 3416-20. PMID 23506199 DOI: 10.1021/Jo400104Q |
0.589 |
|
2013 |
Jack K, Fatila E, Hillis C, Tam W. Ruthenium-catalyzed nucleophilic ring-opening reactions of 7-oxabenzonorbornadienes with methanol Synthetic Communications. 43: 1181-1187. DOI: 10.1080/00397911.2011.626140 |
0.559 |
|
2013 |
Raheem MA, Tam W. Synthesis of C1-substituted 7-oxanorbornadienes Synthetic Communications. 43: 260-267. DOI: 10.1080/00397911.2011.596640 |
0.544 |
|
2013 |
Jack K, Machin B, Tigchelaar A, Tam W. Synthesis of substituted norbornadienes Current Organic Synthesis. 10: 584-630. |
0.351 |
|
2012 |
Tigchelaar A, Tam W. Iridium-catalyzed intramolecular [4 + 2] cycloadditions of alkynyl halides. Beilstein Journal of Organic Chemistry. 8: 1765-70. PMID 23209510 DOI: 10.3762/Bjoc.8.201 |
0.527 |
|
2012 |
Lough AJ, Jack K, Tam W. Hexamethyl 13,14-dioxapenta-cyclo-[8.2.1.1(4,7).0(2,9).0(3,8)]tetra-deca-5,11-diene-1,4,5,6,11,12-hexa-carboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 68: o2963. PMID 23125745 DOI: 10.1107/S1600536812039232 |
0.362 |
|
2012 |
Lough AJ, Jack K, Tam W. Tetra-tert-butyl 13,14-dioxapenta-cyclo-[8.2.1.1(4,7).0(2,9).0(3,8)]tetra-deca-5,11-diene-5,6,11,12-tetra-carboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 68: o2962. PMID 23125744 DOI: 10.1107/S1600536812039220 |
0.353 |
|
2012 |
Lough AJ, Jack K, Tam W. Tetra-methyl 1,4-dimethyl-13,14-dioxa-penta-cyclo-[8.2.1.1(4,7).0(2,9).0(3,8)]tetra-deca-5,11-diene-5,6,11,12-tetra-carboxyl-ate. Acta Crystallographica. Section E, Structure Reports Online. 68: o2961. PMID 23125743 DOI: 10.1107/S1600536812039219 |
0.36 |
|
2012 |
Haner J, Jack K, Menard ML, Howell J, Nagireddy J, Raheem MA, Tam W. Synthesis of C1-substituted oxabenzonorbornadienes Synthesis (Germany). 44: 2713-2722. DOI: 10.1055/S-0032-1316686 |
0.544 |
|
2011 |
Lough AJ, Petrone DA, Tam W. (1S,2S,4R)-7-tert-But-oxy-bicyclo-[2.2.1]hept-5-en-2-yl (2S)-2-(6-meth-oxy-naphthalen-2-yl)propano-ate. Acta Crystallographica. Section E, Structure Reports Online. 67: o1848. PMID 21837213 DOI: 10.1107/S1600536811024238 |
0.327 |
|
2011 |
Kettles TJ, Cockburn N, Tam W. Ruthenium-catalyzed homo Diels-Alder [2 + 2 + 2] cycloadditions of alkynyl phosphonates with bicyclo[2.2.1]hepta-2,5-diene. The Journal of Organic Chemistry. 76: 6951-7. PMID 21732634 DOI: 10.1021/Jo2010928 |
0.598 |
|
2011 |
Durham R, Mandel J, Blanchard N, Tam W. Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3- azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes Canadian Journal of Chemistry. 89: 1494-1505. DOI: 10.1139/v11-135 |
0.468 |
|
2011 |
Haner J, Jack K, Nagireddy J, Raheem MA, Durham R, Tam W. Synthesis of 2-substituted furans by iron- and palladium-catalyzed coupling reactions Synthesis. 731-738. DOI: 10.1055/S-0030-1259484 |
0.52 |
|
2010 |
Raheem MA, Nagireddy JR, Durham R, Tam W. Efficient procedure for the preparation of 2-bromofuran and its application in the synthesis of 2-arylfurans Synthetic Communications. 40: 2138-2146. DOI: 10.1080/00397910903219534 |
0.424 |
|
2010 |
Tam W, Cockburn N. Thieme chemistry journal awardees - Where are they now? Bicyclic alkenes: From cycloadditions to the discovery of new reactions Synlett. 1170-1189. DOI: 10.1055/S-0029-1219780 |
0.614 |
|
2009 |
Lough AJ, Machin BP, Tam W. tert-Butyl N-hydr-oxy-N-[(1S*,2R*)-2-(1-naphth-yl)cyclo-pent-3-en-1-yl]carbamate. Acta Crystallographica. Section E, Structure Reports Online. 65: o1481. PMID 21582783 DOI: 10.1107/S1600536809020315 |
0.303 |
|
2009 |
Goodreid JD, Jennings MC, Tam W. Asymmetric ruthenium-catalysed [2+2] cycloadditions between bicyclic alkenes and chiral aryl-substituted acetylenic acyl camphorsultam alkynes. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o649-52. PMID 19966451 DOI: 10.1107/S0108270109045284 |
0.331 |
|
2009 |
Machin BP, Ballantine M, Mandel J, Blanchard N, Tam W. Rhodium-catalyzed ring-opening reactions of a 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with arylboronic acids. The Journal of Organic Chemistry. 74: 7261-6. PMID 19731959 DOI: 10.1021/Jo901248W |
0.535 |
|
2009 |
Ballantine M, Menard ML, Tam W. Isomerization of 7-oxabenzonorbornadienes into naphthols catalyzed by [RuCl(2)(CO)(3)](2). The Journal of Organic Chemistry. 74: 7570-3. PMID 19725525 DOI: 10.1021/Jo901504N |
0.495 |
|
2009 |
Cockburn N, Karimi E, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions of bicyclic alkenes with alkynyl phosphonates. The Journal of Organic Chemistry. 74: 5762-5. PMID 19572573 DOI: 10.1021/Jo9010206 |
0.588 |
|
2009 |
Machin BP, Howell J, Mandel J, Blanchard N, Tam W. Ruthenium-catalyzed nucleophilic ring-opening reactions of a 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with alcohols. Organic Letters. 11: 2077-80. PMID 19361204 DOI: 10.1021/Ol900454Q |
0.485 |
|
2009 |
Tam W, Goodreid J, Cockburn N. Transition metal-catalyzed [2+2] cycloaddition reactions between bicyclic alkenes and alkynes Current Organic Synthesis. 6: 219-238. DOI: 10.2174/157017909788921907 |
0.437 |
|
2009 |
Tsui GC, Marquand PL, Allen A, Tam W. Synthesis of anti-2,7-disubstituted norbornadienes Synthesis. 609-619. DOI: 10.1055/S-0028-1083352 |
0.792 |
|
2009 |
Howell J, Goddard JD, Tam W. A relative approach for determining ring strain energies of heterobicyclic alkenes Tetrahedron. 65: 4562-4568. DOI: 10.1016/J.Tet.2009.03.090 |
0.328 |
|
2008 |
Le Marquand P, Tsui GC, Whitney JCC, Tam W. Iron-catalyzed cross-coupling reactions between a bicyclic alkenyl triflate and Grignard reagents Journal of Organic Chemistry. 73: 7829-7832. PMID 18771327 DOI: 10.1021/Jo801384E |
0.806 |
|
2008 |
Le Marquand P, Tam W. Enantioselective palladium-catalyzed trimethylenemethane [3+2] cycloadditions. Angewandte Chemie (International Ed. in English). 47: 2926-8. PMID 18338416 DOI: 10.1002/Anie.200705481 |
0.563 |
|
2008 |
Allen A, Villeneuve K, Cockburn N, Fatila E, Riddell N, Tam W. Alkynyl halides in ruthenium(II)-catalyzed [2+2] cycloadditions of bicyclic alkenes European Journal of Organic Chemistry. 4178-4192. DOI: 10.1002/Ejoc.200800424 |
0.523 |
|
2008 |
Jordan RW, Le Marquand P, Tam W. Ruthenium(II)-catalyzed [2+2] cycloadditions of anti 7-substituted norbornenes European Journal of Organic Chemistry. 80-86. DOI: 10.1002/Ejoc.200700706 |
0.47 |
|
2007 |
Allen A, Le Marquand P, Burton R, Villeneuve K, Tam W. Rhodium-catalyzed asymmetric cyclodimerization of oxabenzonorbornadienes and azabenzonorbornadienes: scope and limitations. The Journal of Organic Chemistry. 72: 7849-57. PMID 17880240 DOI: 10.1021/Jo7012884 |
0.56 |
|
2007 |
Burton RR, Tam W. Study on the reactivity of oxabicyclic alkenes in ruthenium-catalyzed [2+2] cycloadditions. The Journal of Organic Chemistry. 72: 7333-6. PMID 17691846 DOI: 10.1021/Jo701383D |
0.456 |
|
2007 |
Burton RR, Tam W. Ruthenium(II)-catalyzed cyclization of azabenzonorbornadienes with alkynes. Organic Letters. 9: 3287-90. PMID 17658753 DOI: 10.1021/Ol0712531 |
0.412 |
|
2007 |
Villeneuve K, Tam W. Construction of isochromenes via a ruthenium-catalyzed reaction of oxabenzonorbornenes with propargylic alcohols Organometallics. 26: 6082-6090. DOI: 10.1021/Om7004518 |
0.5 |
|
2007 |
Liu P, Tam W, Goddard JD. Ruthenium-catalyzed [2+2] cycloadditions between substituted alkynes and norbornadiene: a theoretical study Tetrahedron. 63: 7659-7666. DOI: 10.1016/J.Tet.2007.05.030 |
0.485 |
|
2006 |
Jordan RW, Villeneuve K, Tam W. Study on the reactivity of the alkyne component in ruthenium-catalyzed [2 + 2] cycloadditions between an alkene and an alkyne. The Journal of Organic Chemistry. 71: 5830-3. PMID 16839178 DOI: 10.1021/Jo060864O |
0.404 |
|
2006 |
Liu P, Jordan RW, Kibbee SP, Goddard JD, Tam W. Remote substituent effects in ruthenium-catalyzed [2+2] cycloadditions: an experimental and theoretical study. The Journal of Organic Chemistry. 71: 3793-803. PMID 16674052 DOI: 10.1021/Jo060103L |
0.382 |
|
2006 |
Villeneuve K, Tam W. Ruthenium-catalyzed isomerization of oxa/azabicyclic alkenes: an expedient route for the synthesis of 1,2-naphthalene oxides and imines. Journal of the American Chemical Society. 128: 3514-5. PMID 16536513 DOI: 10.1021/Ja058621L |
0.49 |
|
2006 |
Riddell N, Tam W. Ruthenium-catalyzed [2+2] cycloadditions of alkynyl sulfides and alkynyl sulfones. The Journal of Organic Chemistry. 71: 1934-7. PMID 16496978 DOI: 10.1021/Jo052295A |
0.555 |
|
2006 |
Lough AJ, Villeneuve K, Tam W. Absolute configuration of the p-nitrobenzoate ester of the cycloadduct of (S)-4-hydroxy-2-pentynoate and acetic acid 8-acetoxy-1,4-dihydro-1,4- methanonapththalen-5-yl ester Acta Crystallographica Section E: Structure Reports Online. 62: o2846-o2847. DOI: 10.1107/S1600536806022021 |
0.327 |
|
2006 |
Villeneuve K, Tam W. Ruthenium-catalyzed processes: Dual [2+2] cycloaddition versus cyclopropanation of bicyclic alkenes with propargylic alcohols Organometallics. 25: 843-848. DOI: 10.1021/Om050780Q |
0.416 |
|
2006 |
Burton RR, Tam W. Ruthenium-catalyzed [2+2] cycloadditions between C1-substituted 7-oxanorbornadienes and alkynes Tetrahedron Letters. 47: 7185-7189. DOI: 10.1016/J.Tetlet.2006.07.155 |
0.483 |
|
2006 |
Villeneuve K, Riddell N, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions of bicyclic alkenes and ynamides Tetrahedron. 62: 3823-3836. DOI: 10.1016/J.Tet.2005.11.081 |
0.552 |
|
2006 |
Villeneuve K, Tam W. Ruthenium(II)-catalyzed cyclization of oxabenzonorbornenes with propargylic alcohols: Formation of isochromenes European Journal of Organic Chemistry. 5449-5453. DOI: 10.1002/Ejoc.200600836 |
0.439 |
|
2005 |
Yoo WJ, Allen A, Villeneuve K, Tam W. Rhodium-catalyzed intramolecular [4 + 2] cycloadditions of alkynyl halides. Organic Letters. 7: 5853-6. PMID 16354083 DOI: 10.1055/S-2006-931952 |
0.585 |
|
2005 |
Riddell N, Villeneuve K, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions of ynamides. Organic Letters. 7: 3681-4. PMID 16092849 DOI: 10.1021/Ol0512841 |
0.593 |
|
2005 |
Yoo WJ, Tsui GC, Tam W. Palladium-catalyzed Suzuki couplings of 2,3-dibromonorbornadiene: Synthesis of symmetrical and unsymmetrical aryl-substituted norbornadienes European Journal of Organic Chemistry. 1044-1051. DOI: 10.1002/Ejoc.200400713 |
0.807 |
|
2005 |
Tam W. Ruthenium in Organic Synthesis. Edited by Shun‐Ichi Murahashi. Angewandte Chemie. 44: 6269-6270. DOI: 10.1002/Anie.200485282 |
0.312 |
|
2005 |
Tam W. Ruthenium in Organic Synthesis. Herausgegeben von Shun-Ichi Murahashi. Angewandte Chemie. 117: 6425-6425. DOI: 10.1002/Ange.200485282 |
0.313 |
|
2004 |
Jordan RW, Khoury PR, Goddard JD, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions between 7-substituted norbornadienes and alkynes: an experimental and theoretical study. The Journal of Organic Chemistry. 69: 8467-74. PMID 15549822 DOI: 10.1021/Jo048590X |
0.469 |
|
2004 |
Villeneuve K, Riddell N, Jordan RW, Tsui GC, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions between bicyclic alkenes and alkynyl halides. Organic Letters. 6: 4543-6. PMID 15548071 DOI: 10.1021/Ol048111G |
0.808 |
|
2004 |
Villeneuve K, Tam W. Asymmetric induction in ruthenium-catalyzed [2+2] cycloadditions between bicyclic alkenes and a chiral acetylenic acyl sultam. Angewandte Chemie (International Ed. in English). 43: 610-3. PMID 14743417 DOI: 10.1002/Anie.200352555 |
0.51 |
|
2004 |
Villeneuve K, Riddell N, Jordan RW, Tsui GC, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions between bicyclic alkenes and alkynyl halides Organic Letters. 6: 4543-4546. DOI: 10.1021/ol048111g |
0.812 |
|
2004 |
Khoury PR, Goddard JD, Tam W. Ring strain energies: Substituted rings, norbornanes, norbornenes and norbornadienes Tetrahedron. 60: 8103-8112. DOI: 10.1016/J.Tet.2004.06.100 |
0.4 |
|
2003 |
Jordan RW, Tam W, Lough AJ. Ethyl 7-exo-acetoxy-4-phenyltricyclo-[4.2.1.02,5]non-3-ene-3- carboxylate Acta Crystallographica Section E: Structure Reports Online. 59: o1687-o1688. DOI: 10.1107/S160053680302227X |
0.308 |
|
2003 |
Tam W, Lough AJ, Jordan RW. Ethyl 7-oxo-4-phenyltricyclo[4.2.1.02,5]-non-3-ene-3-carboxylate Acta Crystallographica Section E: Structure Reports Online. 59: o1685-o1686. DOI: 10.1107/S1600536803022244 |
0.303 |
|
2003 |
Villeneuve K, Jordan RW, Tam W. Diastereoselective Ruthenium-Catalyzed [2+2] Cycloadditions between Bicyclic Alkenes and a Chiral Propargylic Alcohol and its Derivatives Synlett. 2123-2128. DOI: 10.1055/S-2003-42108 |
0.418 |
|
2002 |
Tranmer GK, Tam W. Molybdenum-mediated cleavage reactions of isoxazoline rings fused in bicyclic frameworks. Organic Letters. 4: 4101-4. PMID 12423096 DOI: 10.1021/Ol026846K |
0.544 |
|
2002 |
Tranmer GK, Tam W. Palladium-catalyzed Sonogashira coupling of 2,3-dibromonorbornadiene: Synthesis of symmetrical and unsymmetrical norbornadiene-2,3-diynes Synthesis. 1675-1682. DOI: 10.1055/S-2002-33651 |
0.482 |
|
2002 |
Tam W. Topics in Current Chemistry 219. Cross-Coupling Reactions: A Practical Guide Edited by Norio Miyaura (Hokkaido University). Springer-Verlag: Berlin, Heidelberg, New York. 2002. x + 248 pp. $169.00. ISBN 3-540-42175-0. Journal of the American Chemical Society. 124: 12630-12630. DOI: 10.1021/Ja0252532 |
0.339 |
|
2002 |
Jordan RW, Tam W. Reactivity of the alkene component in the ruthenium-catalyzed [2+2] cycloaddition between an alkene and an alkyne: Part 2 Tetrahedron Letters. 43: 6051-6054. DOI: 10.1016/S0040-4039(02)01191-7 |
0.531 |
|
2002 |
Mayo P, Tam W. Palladium-catalyzed hydrophenylation of bicyclic alkenes Tetrahedron. 58: 9527-9540. DOI: 10.1016/S0040-4020(02)01277-2 |
0.605 |
|
2002 |
Mayo P, Tam W. Ring-opening metathesis - Cross-metathesis reactions (ROM-CM) of substituted norbornadienes and norbornenes Tetrahedron. 58: 9513-9525. DOI: 10.1016/S0040-4020(02)01276-0 |
0.592 |
|
2001 |
Jordan RW, Tam W. Study on the reactivity of the alkene component in ruthenium-catalyzed [2 + 2] cycloadditions between an alkene and an alkyne. Part 1 Organic Letters. 3: 2367-2370. PMID 11463318 DOI: 10.1021/Ol016174I |
0.571 |
|
2001 |
Mayo P, Orlova G, Goddard JD, Tam W. Remote substituent effects on the oxymercuration of 2-substituted norbornenes: An experimental and theoretical study Journal of Organic Chemistry. 66: 5182-5191. PMID 11463272 DOI: 10.1021/Jo010330H |
0.413 |
|
2001 |
Tranmer GK, Tam W. Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrones Journal of Organic Chemistry. 66: 5113-5123. PMID 11463264 DOI: 10.1021/Jo015610B |
0.503 |
|
2001 |
Yip C, Handerson S, Tranmer GK, Tam W. Intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrile oxides Journal of Organic Chemistry. 66: 276-286. PMID 11429911 DOI: 10.1021/jo005611o |
0.339 |
|
2001 |
Mayo P, Tam W. Remote substituent effects on regioselectivity in the Pauson-Khand reaction of 2-substituted norbornenes Tetrahedron. 57: 5943-5952. DOI: 10.1016/S0040-4020(01)00574-9 |
0.531 |
|
2001 |
Mayo P, Hecnar T, Tam W. 1,3-Dipolar cycloaddition of nitrile oxides with unsymmetrically substituted norbornenes Tetrahedron. 57: 5931-5941. DOI: 10.1016/S0040-4020(01)00573-7 |
0.469 |
|
2000 |
Jordan RW, Tam W. Ruthenium-catalyzed [2 + 2] cycloadditions of 2-substituted norbornenes Organic Letters. 2: 3031-3034. PMID 10986100 DOI: 10.1021/Ol006397T |
0.531 |
|
2000 |
Tranmer GK, Yip C, Handerson S, Jordan RW, Tam W. Synthesis of 2,3-disubstituted norbornadienes Canadian Journal of Chemistry. 78: 527-535. DOI: 10.1139/V00-047 |
0.521 |
|
2000 |
Tranmer GK, Keech P, Tam W. Intramolecular 1,3-dipolar cycloadditions of 2-substituted norbornadiene-tethered nitrones Chemical Communications. 863-864. DOI: 10.1039/B001543L |
0.476 |
|
1999 |
Yip C, Handerson S, Jordan R, Tam W. Highly regio- and stereoselective intramolecular 1,3-dipolar cycloadditions of norbornadiene-tethered nitrile oxides Organic Letters. 1: 791-794. DOI: 10.1021/Ol990765F |
0.452 |
|
1999 |
Mayo P, Poirier M, Rainey J, Tam W. Effect of a remote substituent on regioselectivity in oxymercuration of unsymmetrically substituted norbornenes Tetrahedron Letters. 40: 7727-7730. DOI: 10.1016/S0040-4039(99)01635-4 |
0.467 |
|
1997 |
Barrett AGM, Tam W. Regioselective Ring Opening of Vinylcyclopropanes by Hydrogenation with Palladium on Activated Carbon Journal of Organic Chemistry. 62: 7673-7678. DOI: 10.1021/Jo970879+ |
0.414 |
|
1997 |
Barrett AGM, Tam W. Studies on Mercury(II)-Mediated Opening of Bi- and Tercyclopropane Arrays Journal of Organic Chemistry. 62: 4653-4664. DOI: 10.1021/Jo970464O |
0.392 |
|
1997 |
Lautens M, Tam W, Blackwell J. Synthesis of highly functionalized diquinanes by the regio- and stereoselective cleavage of homo-Diels-Alder cycloadducts Journal of the American Chemical Society. 119: 623-624. DOI: 10.1021/Ja962223O |
0.595 |
|
1996 |
Lautens M, Klute W, Tam W. Transition Metal-Mediated Cycloaddition Reactions. Chemical Reviews. 96: 49-92. PMID 11848744 DOI: 10.1021/Cr950016L |
0.529 |
|
1995 |
Lautens M, Lough AJ, Tam W. An Unusual trans-Fused Cyclopentane Ring System at 158 K Acta Crystallographica Section C Crystal Structure Communications. 51: 1944-1946. DOI: 10.1107/S0108270195003490 |
0.513 |
|
1995 |
Lautens M, Edwards LG, Tam W, Lough AJ. Nickel-catalyzed [2.pi. + 2.pi. + 2.pi.] (homo-Diels-Alder) and [2.pi. + 2.pi.] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes. Journal of the American Chemical Society. 117: 10276-10291. DOI: 10.1021/Ja00146A012 |
0.53 |
|
1995 |
Lautens M, Tam W, Lautens JC, Edwards LG, Crudden CM, Smith AC. Cobalt-Catalyzed [2.pi. + 2.pi. + 2.pi.] (Homo-Diels-Alder) and [2.pi. + 2.pi. + 4.pi.] Cycloadditions of Bicyclo[2.2.1]hepta-2,5-dienes Journal of the American Chemical Society. 117: 6863-6879. DOI: 10.1021/Ja00131A008 |
0.639 |
|
1995 |
Lautens M, Tam W, Lautens JC, Edwards LG, Crudden CM, Smith AC. Cobalt-catalyzed [2π + 2π + 2π] (homo Diels-Alder) and [2π + 2π + 4π] cycloadditions of bicyclo[2.2.1]hepta-2,5-dienes Journal of the American Chemical Society. 117: 6863-6879. |
0.55 |
|
1994 |
Lautens M, Tam W, Edwards LG. Stereoselectivity in the homo-Diels–Alder reaction: effect of a remote 7-substituent on nickel-catalysed cycloadditions Journal of the Chemical Society-Perkin Transactions 1. 2143-2150. DOI: 10.1039/P19940002143 |
0.65 |
|
1994 |
Lautens M, Tam W, Edwards LG. Stereoselectivity in the homo-Diels-Alder reaction: Effect of a remote 7-Substituent on nickel-catalysed cycloadditions Journal of the Chemical Society, Perkin Transactions 1. 2143-2150. |
0.462 |
|
1993 |
Lautens M, Tam W, Sood C. Enantioselective cobalt-catalyzed [4.pi.+2.pi.+2.pi.] cycloadditions The Journal of Organic Chemistry. 58: 4513-4515. DOI: 10.1021/Jo00069A003 |
0.678 |
|
1993 |
Lautens M, Tam W, Sood C. Enantioselective cobalt-catalyzed [4π + 2π + 2π] cycloadditions Journal of Organic Chemistry. 58: 4513-4515. |
0.332 |
|
1992 |
Lautens M, Tam W, Edwards LG. Cobalt-catalyzed intramolecular homo Diels-Alder reactions The Journal of Organic Chemistry. 57: 8-9. DOI: 10.1021/Jo00027A005 |
0.661 |
|
1992 |
Lautens M, Tam W, Edwards LG. Cobalt-catalyzed intramolecular homo Diels-Alder reactions Journal of Organic Chemistry. 57: 8-9. |
0.461 |
|
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