Year |
Citation |
Score |
2023 |
Fu J, Lundy W, Chowdhury R, Twitty JC, Dinh LP, Sampson J, Lam YH, Sevov CS, Watson MP, Kalyani D. Nickel-Catalyzed Electroreductive Coupling of Alkylpyridinium Salts and Aryl Halides. Acs Catalysis. 13: 9336-9345. PMID 38188282 DOI: 10.1021/acscatal.3c01939 |
0.759 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Organic & Inorganic Au. 3: 321-327. PMID 38075448 DOI: 10.1021/acsorginorgau.3c00050 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Central Science. 9: 1846-1852. PMID 37901169 DOI: 10.1021/acscentsci.3c01136 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Acs Medicinal Chemistry Letters. 14: 1311-1317. PMID 37849544 DOI: 10.1021/acsmedchemlett.3c00412 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Biochemistry. PMID 37772735 DOI: 10.1021/acs.biochem.3c00495 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Organic Letters. PMID 37772728 DOI: 10.1021/acs.orglett.3c03103 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. Journal of Medicinal Chemistry. PMID 37772719 DOI: 10.1021/acs.jmedchem.3c01704 |
0.65 |
|
2023 |
Cantor EH, Faul MM, Huryn DM, Kallander L, Ruck RT, Watson MP. Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back. The Journal of Organic Chemistry. PMID 37772717 DOI: 10.1021/acs.joc.3c02082 |
0.65 |
|
2023 |
Baker KM, Bercher OP, Twitty JC, Mortimer T, Watson MP. 2,6-Bis(pyrazol-1-yl)pyridine (1-bpp) as a General Ligand for the Negishi Alkylation of Alkylpyridinium Salts. The Journal of Organic Chemistry. PMID 37368977 DOI: 10.1021/acs.joc.3c00665 |
0.755 |
|
2023 |
Twitty JC, Hong Y, Garcia B, Tsang S, Liao J, Schultz DM, Hanisak J, Zultanski SL, Dion A, Kalyani D, Watson MP. Diversifying Amino Acids and Peptides via Deaminative Reductive Cross-Couplings Leveraging High-Throughput Experimentation. Journal of the American Chemical Society. PMID 36853652 DOI: 10.1021/jacs.2c11451 |
0.729 |
|
2021 |
Tcyrulnikov S, Cai Q, Twitty JC, Xu J, Atifi A, Bercher OP, Yap GPA, Rosenthal J, Watson MP, Kozlowski MC. Dissection of Alkylpyridinium Structures to Understand Deamination Reactions. Acs Catalysis. 11: 8456-8466. PMID 34745709 DOI: 10.1021/acscatal.1c01860 |
0.751 |
|
2021 |
Xu J, Twitty JC, Watson MP. Nickel-Catalyzed Deaminative Cyanation: Nitriles and One-Carbon Homologation from Alkyl Amines. Organic Letters. PMID 34328332 DOI: 10.1021/acs.orglett.1c01959 |
0.759 |
|
2021 |
Xu J, Bercher OP, Watson MP. Overcoming the Naphthyl Requirement in Stereospecific Cross-Couplings to Form Quaternary Stereocenters. Journal of the American Chemical Society. PMID 34062058 DOI: 10.1021/jacs.1c03898 |
0.308 |
|
2021 |
Xu J, Bercher OP, Talley MR, Watson MP. Nickel-Catalyzed, Stereospecific C-C and C-B Cross-Couplings via C-N and C-O Bond Activation. Acs Catalysis. 11: 1604-1612. PMID 33986970 DOI: 10.1021/acscatal.0c05484 |
0.35 |
|
2020 |
Wang J, Hoerrner M, Watson MP, Weix DJ. Nickel-Catalyzed Synthesis of Dialkyl Ketones from the Coupling of N-Alkyl Pyridinium Salts with Activated Carboxylic Acids. Angewandte Chemie (International Ed. in English). PMID 32374951 DOI: 10.1002/Anie.202002271 |
0.512 |
|
2020 |
Xu J, Watson MP. Stitching two chiral centers with one catalyst. Science (New York, N.Y.). 367: 509-510. PMID 32001642 DOI: 10.1126/Science.Aba4222 |
0.336 |
|
2019 |
Baker KM, Lucas Baca D, Plunkett S, Daneker ME, Watson MP. Engaging Alkenes and Alkynes in Deaminative Alkyl-Alkyl and Alkyl-Vinyl Cross-Couplings of Alkylpyridinium Salts. Organic Letters. PMID 31763855 DOI: 10.1021/Acs.Orglett.9B03899 |
0.42 |
|
2019 |
Hoerrner ME, Baker KM, Basch CH, Bampo EM, Watson MP. Deaminative Arylation of Amino Acid-derived Pyridinium Salts. Organic Letters. PMID 31464131 DOI: 10.1021/Acs.Orglett.9B02643 |
0.418 |
|
2019 |
Liao J, Basch CH, Hoerrner ME, Talley MR, Boscoe BP, Tucker JW, Garnsey MR, Watson MP. Deaminative Reductive Cross-Electrophile Couplings of Alkylpyridinium Salts and Aryl Bromides. Organic Letters. PMID 30917282 DOI: 10.1021/Acs.Orglett.9B01014 |
0.466 |
|
2019 |
Plunkett S, Basch CH, Santana SO, Watson MP. Harnessing Alkyl Pyridinium Salts as Electrophiles in Deaminative Alkyl-Alkyl Cross-Couplings. Journal of the American Chemical Society. PMID 30682254 DOI: 10.1021/Jacs.9B00111 |
0.462 |
|
2018 |
Pound SM, Watson MP. Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives. Chemical Communications (Cambridge, England). PMID 30283929 DOI: 10.1039/C8Cc07093H |
0.744 |
|
2018 |
Guan W, Liao J, Watson MP. Vinylation of Benzylic Amines via C-N Bond Functionalization of Benzylic Pyridinium Salts. Synthesis. 50: 3231-3237. PMID 30174353 DOI: 10.1055/S-0037-1610084 |
0.461 |
|
2018 |
Liao J, Guan W, Boscoe BP, Tucker JW, Tomlin JW, Garnsey MR, Watson MP. Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C-N Bond Activation. Organic Letters. PMID 29745674 DOI: 10.1021/Acs.Orglett.8B01062 |
0.487 |
|
2017 |
Cobb KM, Rabb-Lynch JM, Hoerrner ME, Manders A, Zhou Q, Watson MP. Stereospecific, Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Allylic Pivalates To Deliver Quaternary Stereocenters. Organic Letters. PMID 28783357 DOI: 10.1021/Acs.Orglett.7B02063 |
0.491 |
|
2017 |
Basch CH, Liao J, Xu J, Piane JJ, Watson MP. Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C-N Bond Activation. Journal of the American Chemical Society. PMID 28359153 DOI: 10.1021/Jacs.7B02389 |
0.458 |
|
2016 |
Dasgupta S, Liu J, Shoffler CA, Yap GP, Watson MP. Enantioselective, Copper-Catalyzed Alkynylation of Ketimines To Deliver Isoquinolines with α-Diaryl Tetrasubstituted Stereocenters. Organic Letters. 18: 6006-6009. PMID 27934382 DOI: 10.1021/Acs.Orglett.6B02787 |
0.423 |
|
2016 |
Zhou Q, Cobb KM, Tan T, Watson MP. Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity. Journal of the American Chemical Society. PMID 27610831 DOI: 10.1021/Jacs.6B08075 |
0.465 |
|
2016 |
Zhou Q, Srinivas HD, Zhang S, Watson MP. Accessing Both Retention and Inversion Pathways in Stereospecific, Nickel-Catalyzed Miyaura Borylations of Allylic Pivalates. Journal of the American Chemical Society. PMID 27589327 DOI: 10.1021/Jacs.6B07396 |
0.418 |
|
2015 |
Ehle AR, Morris MG, Klebon BD, Yap GP, Watson MP. Stereoselective Synthesis of Trisubstituted Vinyl Bromides by Addition of Alkynes to Oxocarbenium Ions. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 26: 2702-2706. PMID 27482143 DOI: 10.1055/S-0035-1560265 |
0.434 |
|
2015 |
Liu J, Dasgupta S, Watson MP. Enantioselective additions of copper acetylides to cyclic iminium and oxocarbenium ions. Beilstein Journal of Organic Chemistry. 11: 2696-706. PMID 26877791 DOI: 10.3762/Bjoc.11.290 |
0.366 |
|
2015 |
Basch CH, Cobb KM, Watson MP. Nickel-Catalyzed Borylation of Benzylic Ammonium Salts: Stereospecific Synthesis of Enantioenriched Benzylic Boronates. Organic Letters. PMID 26679212 DOI: 10.1021/Acs.Orglett.5B03455 |
0.518 |
|
2015 |
Dasgupta S, Rivas T, Watson MP. Enantioselective Copper(I)-Catalyzed Alkynylation of Oxocarbenium Ions to Set Diaryl Tetrasubstituted Stereocenters. Angewandte Chemie (International Ed. in English). PMID 26403641 DOI: 10.1002/Anie.201507373 |
0.405 |
|
2015 |
Haidzinskaya T, Kerchner HA, Liu J, Watson MP. Diastereoselective, Zinc-Catalyzed Alkynylation of α-Bromo Oxocarbenium Ions. Organic Letters. 17: 3857-9. PMID 26196257 DOI: 10.1021/Acs.Orglett.5B01838 |
0.362 |
|
2015 |
Srinivas HD, Maity P, Yap GP, Watson MP. Enantioselective copper-catalyzed alkynylation of benzopyranyl oxocarbenium ions. The Journal of Organic Chemistry. 80: 4003-16. PMID 25847687 DOI: 10.1021/Acs.Joc.5B00364 |
0.413 |
|
2014 |
Shacklady-McAtee DM, Roberts KM, Basch CH, Song YG, Watson MP. A General, Simple Catalyst for Enantiospecific Cross Couplings of Benzylic Ammonium Triflates and Boronic Acids: No Phosphine Ligand Required. Tetrahedron. 70: 4257-4263. PMID 25364060 DOI: 10.1016/J.Tet.2014.03.039 |
0.482 |
|
2014 |
Srinivas HD, Zhou Q, Watson MP. Enantiospecific, nickel-catalyzed cross-couplings of allylic pivalates and arylboroxines. Organic Letters. 16: 3596-9. PMID 24927013 DOI: 10.1021/Ol5016724 |
0.489 |
|
2013 |
Zhou Q, Srinivas HD, Dasgupta S, Watson MP. Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes. Journal of the American Chemical Society. 135: 3307-10. PMID 23425080 DOI: 10.1021/Ja312087X |
0.484 |
|
2013 |
Maity P, Shacklady-McAtee DM, Yap GP, Sirianni ER, Watson MP. Nickel-catalyzed cross couplings of benzylic ammonium salts and boronic acids: stereospecific formation of diarylethanes via C-N bond activation. Journal of the American Chemical Society. 135: 280-5. PMID 23268734 DOI: 10.1021/Ja3089422 |
0.516 |
|
2012 |
Watson MP, Maity P. Controlling Enantioselectivity in Additions to Cyclic Oxocarbenium Ions via Transition Metal Catalysis. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 23: 1705-1708. PMID 25382939 DOI: 10.1055/S-0031-1290697 |
0.337 |
|
2012 |
Ehle AR, Zhou Q, Watson MP. Nickel(0)-catalyzed Heck cross-coupling via activation of aryl C-OPiv bonds. Organic Letters. 14: 1202-5. PMID 22335199 DOI: 10.1021/Ol203322V |
0.424 |
|
2011 |
Maity P, Srinivas HD, Watson MP. Copper-catalyzed enantioselective additions to oxocarbenium ions: alkynylation of isochroman acetals. Journal of the American Chemical Society. 133: 17142-5. PMID 21988178 DOI: 10.1021/Ja207585P |
0.391 |
|
2011 |
Shacklady-McAtee DM, Dasgupta S, Watson MP. Nickel(0)-catalyzed cyclization of N-benzoylaminals for isoindolinone synthesis. Organic Letters. 13: 3490-3. PMID 21644568 DOI: 10.1021/Ol201248C |
0.479 |
|
2008 |
Watson MP, Jacobsen EN. Asymmetric intramolecular arylcyanation of unactivated olefins via C-CN bond activation. Journal of the American Chemical Society. 130: 12594-5. PMID 18761453 DOI: 10.1021/Ja805094J |
0.583 |
|
2007 |
Watson MP, Overman LE, Bergman RG. Kinetic and computational analysis of the palladium(II)-catalyzed asymmetric allylic trichloroacetimidate rearrangement: development of a model for enantioselectivity. Journal of the American Chemical Society. 129: 5031-44. PMID 17402733 DOI: 10.1021/Ja0676962 |
0.653 |
|
2007 |
Anderson CE, Kirsch SF, Overman LE, Richards CJ, Watson MP. Preparation of the cop catalysts: [(S)-COP-OAc]2, [(S)-COP-Cl]2, and (S)-COP-hfacac Organic Syntheses. 84: 148-155. DOI: 10.1002/0471264229.Os084.15 |
0.712 |
|
2007 |
Anderson CE, Overman LE, Richards CJ, Watson MP, White N. Preparation of (η5‐(S)‐2‐(4‐Methylethyl)‐Oxazolinylcyclopentadienyl)‐(η4‐Tetraphenylcyclo‐Butadiene)cobalt Organic Syntheses. 139-147. DOI: 10.1002/0471264229.Os084.14 |
0.742 |
|
2007 |
Anderson CE, Overman LE, Richards CJ, Watson MP, White N. Preparation of (η5-(S)-2-(4-methylethyl)- oxazolinylcyclopentadienyl)-(η4-tetraphenylcyclo-butadiene) cobalt (cobalt, [1,1′,1″,1‴-(η4-1,3- cyclobutadiene-1,2,3,4-tetrayl)tetrakis [benzene]] [(1,2,3,4,5-η)-1-[(4S)-4, 5-dihydro-4-(1-methylethyl)-2-oxazolyl]-2,4-cyclopentadien-1-yl]) Organic Syntheses. 84: 139-147. |
0.689 |
|
2005 |
Anderson CE, Overman LE, Watson MP. Asymmetric Rearrangement of Allylic Trichloroacetimidates: Preparation of (S)‐2,2,2‐Trichloro‐N‐(1‐propylallyl)acetamide Organic Syntheses. 134-139. DOI: 10.1002/0471264229.Os082.21 |
0.555 |
|
2005 |
Anderson CE, Overman LE, Watson MP. Asymmetric rearrangement of allylic trichloroacetimidates: Preparation of (S)-2,2,2-trichloro-N-(1-propylallyl)acetamide Organic Syntheses. 82: 134-139. |
0.626 |
|
2004 |
Kirsch SF, Overman LE, Watson MP. Monomeric cobalt oxazoline palladacycles (COP). Useful catalysts for catalytic asymmetric rearrangement of allylic trichloroacetimidates. The Journal of Organic Chemistry. 69: 8101-4. PMID 15527296 DOI: 10.1021/Jo0487092 |
0.666 |
|
Show low-probability matches. |