Foscato M, Occhipinti G, Hopen Eliasson S, Jensen V
J Chem Inf Model. 2024; 64(2):412-424.
PMID: 38247361
PMC: 10806812.
DOI: 10.1021/acs.jcim.3c01649.
Zachmann R, Yahata K, Holzheimer M, Jarret M, Wirtz C, Furstner A
J Am Chem Soc. 2023; 145(4):2584-2595.
PMID: 36652728
PMC: 9896551.
DOI: 10.1021/jacs.2c12529.
Hicks H, Brown D, Chan H, Sousa B, Christensen K, Burton J
Org Lett. 2022; 24(50):9174-9178.
PMID: 36508492
PMC: 9791679.
DOI: 10.1021/acs.orglett.2c03524.
Biberger T, Nothling N, Leutzsch M, Gordon C, Coperet C, Furstner A
Angew Chem Int Ed Engl. 2022; 61(24):e202201311.
PMID: 35363926
PMC: 9322539.
DOI: 10.1002/anie.202201311.
Charaschanya M, Maskrey T, LaPorte M, Janjic J, Wipf P
ACS Med Chem Lett. 2022; 13(3):403-408.
PMID: 35300093
PMC: 8919392.
DOI: 10.1021/acsmedchemlett.1c00561.
Total Syntheses of Scabrolide A and Nominal Scabrolide B.
Meng Z, Furstner A
J Am Chem Soc. 2022; 144(4):1528-1533.
PMID: 35044751
PMC: 8815080.
DOI: 10.1021/jacs.1c12401.
A Unified Approach to Polycyclic Alkaloids of the Ingenamine Estate: Total Syntheses of Keramaphidin B, Ingenamine, and Nominal Njaoamine I.
Meng Z, Spohr S, Tobegen S, Fares C, Furstner A
J Am Chem Soc. 2021; 143(35):14402-14414.
PMID: 34448391
PMC: 8431342.
DOI: 10.1021/jacs.1c07955.
Light-Driven gem Hydrogenation: An Orthogonal Entry into "Second-Generation" Ruthenium Carbene Catalysts for Olefin Metathesis.
Zachmann R, Furstner A
Chemistry. 2021; 27(28):7663-7666.
PMID: 33871083
PMC: 8251631.
DOI: 10.1002/chem.202101176.
Grubbs Metathesis Enabled by a Light-Driven gem-Hydrogenation of Internal Alkynes.
Biberger T, Zachmann R, Furstner A
Angew Chem Int Ed Engl. 2020; 59(42):18423-18429.
PMID: 32608043
PMC: 7589215.
DOI: 10.1002/anie.202007030.
An Initiation Kinetics Prediction Model Enables Rational Design of Ruthenium Olefin Metathesis Catalysts Bearing Modified Chelating Benzylidenes.
Luo S, Engle K, Dong X, Hejl A, Takase M, Henling L
ACS Catal. 2020; 8(5):4600-4611.
PMID: 32528741
PMC: 7289044.
DOI: 10.1021/acscatal.8b00843.
Room Temperature Ionic Liquids as Green Solvent Alternatives in the Metathesis of Oleochemical Feedstocks.
Thomas P, Marvey B
Molecules. 2016; 21(2).
PMID: 26861282
PMC: 6273002.
DOI: 10.3390/molecules21020184.
Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes.
Flanigan D, Romanov-Michailidis F, White N, Rovis T
Chem Rev. 2015; 115(17):9307-87.
PMID: 25992594
PMC: 4986729.
DOI: 10.1021/acs.chemrev.5b00060.
A cooperative N-heterocyclic carbene/chiral phosphate catalysis system for allenolate annulations.
Lee A, Scheidt K
Angew Chem Int Ed Engl. 2014; 53(29):7594-8.
PMID: 24895280
PMC: 4142640.
DOI: 10.1002/anie.201403446.
Improved metathesis lifetime: chelating pyridinyl-alcoholato ligands in the second generation Grubbs precatalyst.
du Toit J, Jordaan M, Huijsmans C, Jordaan J, van Sittert C, Vosloo H
Molecules. 2014; 19(5):5522-37.
PMID: 24786690
PMC: 6272008.
DOI: 10.3390/molecules19055522.
Evolution of catalytic stereoselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity.
Hoveyda A
J Org Chem. 2014; 79(11):4763-92.
PMID: 24720633
PMC: 4049245.
DOI: 10.1021/jo500467z.
Efficient and selective formation of macrocyclic disubstituted Z alkenes by ring-closing metathesis (RCM) reactions catalyzed by Mo- or W-based monoaryloxide pyrrolide (MAP) complexes: applications to total syntheses of epilachnene, yuzu lactone,....
Wang C, Yu M, Kyle A, Jakubec P, Dixon D, Schrock R
Chemistry. 2013; 19(8):2726-40.
PMID: 23345004
PMC: 3996920.
DOI: 10.1002/chem.201204045.
Divalent and Multivalent Activation in Phosphate Triesters: A Versatile Method for the Synthesis of Advanced Polyol Synthons.
Thomas C, McParland J, Hanson P
European J Org Chem. 2012; 2009(32):5487-5500.
PMID: 23264750
PMC: 3526009.
DOI: 10.1002/ejoc.200900560.
A phosphate tether-mediated, one-pot, sequential ring-closing metathesis/cross-metathesis/chemoselective hydrogenation protocol.
Venukadasula P, Chegondi R, Suryn G, Hanson P
Org Lett. 2012; 14(10):2634-7.
PMID: 22568560
PMC: 3858481.
DOI: 10.1021/ol301007h.
Enol ethers as substrates for efficient Z- and enantioselective ring-opening/cross-metathesis reactions promoted by stereogenic-at-Mo complexes: utility in chemical synthesis and mechanistic attributes.
Yu M, Ibrahem I, Hasegawa M, Schrock R, Hoveyda A
J Am Chem Soc. 2012; 134(5):2788-99.
PMID: 22272931
PMC: 3298191.
DOI: 10.1021/ja210946z.
Metathesis of fatty acid ester derivatives in 1,1-dialkyl and 1,2,3-trialkyl imidazolium type ionic liquids.
Thomas P, Marvey B, Ebenso E
Int J Mol Sci. 2011; 12(6):3989-97.
PMID: 21747719
PMC: 3131603.
DOI: 10.3390/ijms12063989.
