| Year |
Citation |
Score |
| 2024 |
Davies J, Lyonnet JR, Carvalho B, Sahoo B, Day CS, Juliá-Hernández F, Duan Y, Obst M, Norrby PO, Hopmann KH, Martin R. Kinetically-Controlled Ni-Catalyzed Direct Carboxylation of Unactivated Secondary Alkyl Bromides without Chain Walking. Journal of the American Chemical Society. PMID 38193812 DOI: 10.1021/jacs.3c11205 |
0.77 |
|
| 2023 |
Rodrigalvarez J, Haut FL, Martin R. Regiodivergent C-H Functionalization via Ni-Catalyzed Chain-Walking Reactions. Jacs Au. 3: 3270-3282. PMID 38155646 DOI: 10.1021/jacsau.3c00617 |
0.369 |
|
| 2023 |
Odena C, Gómez-Bengoa E, Martin R. Ring Walking Mediated by Ni-Ni Species as a Vehicle for Enabling Distal C(sp)-H Functionalization of Aryl Pivalates. Journal of the American Chemical Society. PMID 38153272 DOI: 10.1021/jacs.3c12497 |
0.35 |
|
| 2023 |
Velasco-Rubio Á, Cong F, Tian Y, Martin R. Ni-Catalyzed 1,2-Alkyl Borylation and Silylation of Allenes En Route to [1,3]-Bis-Organometallic Reagents. Organic Letters. PMID 38095944 DOI: 10.1021/acs.orglett.3c03574 |
0.343 |
|
| 2023 |
Day CS, Martin R. Comproportionation and disproportionation in nickel and copper complexes. Chemical Society Reviews. PMID 37655600 DOI: 10.1039/d2cs00494a |
0.592 |
|
| 2023 |
Zhang H, Rodrigalvarez J, Martin R. C(sp)-H Hydroxylation via Catalytic 1,4-Ni Migration with NO. Journal of the American Chemical Society. PMID 37531410 DOI: 10.1021/jacs.3c07018 |
0.369 |
|
| 2023 |
Talavera L, Freund RRA, Zhang H, Wakeling M, Jensen M, Martin R. Nickel-Catalyzed 1,1-Aminoborylation of Unactivated Terminal Alkenes. Acs Catalysis. 13: 5538-5543. PMID 37404837 DOI: 10.1021/acscatal.3c00888 |
0.316 |
|
| 2023 |
Lv XY, Martin R. Cu-Catalyzed C(sp) Amination of Unactivated Secondary Alkyl Iodides Promoted by Diaryliodonium Salts. Organic Letters. PMID 37195763 DOI: 10.1021/acs.orglett.3c01216 |
0.405 |
|
| 2023 |
Haut FL, Mega RS, Estornell JV, Martin R. Catalytic Photoinduced Intramolecular Decarboxylative and Desulfonylative sp3Allylation Enabled by Sulfinate Salts. Angewandte Chemie (International Ed. in English). e202304084. PMID 37162384 DOI: 10.1002/anie.202304084 |
0.326 |
|
| 2023 |
Chen J, Wang H, Day CS, Martin R. Corrigendum: Nickel-Catalyzed Site-Selective Intermolecular C(sp )-H Amidation. Angewandte Chemie (International Ed. in English). e202301071. PMID 36808859 DOI: 10.1002/anie.202301071 |
0.636 |
|
| 2023 |
Rodrigalvarez J, Wang H, Martin R. Native Amides as Enabling Vehicles for Forging spsp Architectures via Interrupted Deaminative Ni-Catalyzed Chain-Walking. Journal of the American Chemical Society. PMID 36753384 DOI: 10.1021/jacs.2c12915 |
0.344 |
|
| 2022 |
Lv XY, Abrams R, Martin R. Copper-Catalyzed C(sp )-Amination of Ketone-Derived Dihydroquinazolinones by Aromatization-Driven C-C Bond Scission. Angewandte Chemie (International Ed. in English). e202217386. PMID 36576703 DOI: 10.1002/anie.202217386 |
0.357 |
|
| 2022 |
Cong F, Mega RS, Chen J, Day CS, Martin R. Trifluoromethylation of Carbonyl and Unactivated Olefin Derivatives by C(sp )-C Bond Cleavage. Angewandte Chemie (International Ed. in English). e202214633. PMID 36416716 DOI: 10.1002/anie.202214633 |
0.647 |
|
| 2022 |
Chen J, Wang H, Day CS, Martin R. Nickel-Catalyzed Site-Selective Intermolecular C(sp3)-H Amidation. Angewandte Chemie (International Ed. in English). PMID 36254803 DOI: 10.1002/anie.202212983 |
0.655 |
|
| 2022 |
Day CS, Ton SJ, McGuire RT, Foroutan-Nejad C, Martin R. Reductive Elimination from Sterically Encumbered Ni-Polypyridine Complexes. Organometallics. 41: 2662-2667. PMID 36249447 DOI: 10.1021/acs.organomet.2c00362 |
0.593 |
|
| 2022 |
Day CS, Do CD, Odena C, Benet-Buchholz J, Xu L, Foroutan-Nejad C, Hopmann KH, Martin R. Room-Temperature-Stable Magnesium Electride via Ni(II) Reduction. Journal of the American Chemical Society. PMID 35830190 DOI: 10.1021/jacs.2c01807 |
0.574 |
|
| 2022 |
Yue WJ, Day CS, Brenes Rucinski AJ, Martin R. Catalytic Hydrodifluoroalkylation of Unactivated Olefins. Organic Letters. 24: 5109-5114. PMID 35815401 DOI: 10.1021/acs.orglett.2c01941 |
0.602 |
|
| 2022 |
Lv XY, Abrams R, Martin R. Dihydroquinazolinones as adaptative C(sp) handles in arylations and alkylations via dual catalytic C-C bond-functionalization. Nature Communications. 13: 2394. PMID 35504911 DOI: 10.1038/s41467-022-29984-0 |
0.364 |
|
| 2022 |
Sun SZ, Cai YM, Zhang DL, Wang JB, Yao HQ, Rui XY, Martin R, Shang M. Enantioselective Deaminative Alkylation of Amino Acid Derivatives with Unactivated Olefins. Journal of the American Chemical Society. PMID 35029378 DOI: 10.1021/jacs.1c12350 |
0.364 |
|
| 2021 |
He Y, Börjesson M, Song H, Xue Y, Zeng D, Martin R, Zhu S. Nickel-Catalyzed Difunctionalization of Aryl Bromides with Alkynes and Alkyl Bromides via a Vinyl-to-Aryl 1,4-Hydride Shift. Journal of the American Chemical Society. PMID 34793680 DOI: 10.1021/jacs.1c10368 |
0.74 |
|
| 2021 |
Tortajada A, Börjesson M, Martin R. Nickel-Catalyzed Reductive Carboxylation and Amidation Reactions. Accounts of Chemical Research. 54: 3941-3952. PMID 34586783 DOI: 10.1021/acs.accounts.1c00480 |
0.433 |
|
| 2021 |
Jankins TC, Martin-Montero R, Cooper P, Martin R, Engle KM. Low-Valent Tungsten Catalysis Enables Site-Selective Isomerization-Hydroboration of Unactivated Alkenes. Journal of the American Chemical Society. 143: 14981-14986. PMID 34498848 DOI: 10.1021/jacs.1c07162 |
0.393 |
|
| 2021 |
Yue WJ, Day CS, Martin R. Site-Selective Defluorinative sp C-H Alkylation of Secondary Amides. Journal of the American Chemical Society. 143: 6395-6400. PMID 33904726 DOI: 10.1021/jacs.1c03126 |
0.619 |
|
| 2021 |
Davies J, Janssen-Müller D, Zimin DP, Day CS, Yanagi T, Elfert J, Martin R. Ni-Catalyzed Carboxylation of Aziridines en Route to β-Amino Acids. Journal of the American Chemical Society. PMID 33724815 DOI: 10.1021/jacs.1c01916 |
0.596 |
|
| 2021 |
Martin R, Sun SZ, Talavera L, Spiess P, Day C. sp3 Bis-Organometallic Reagents via Catalytic 1,1-Difunctionalization of Unactivated Olefins. Angewandte Chemie (International Ed. in English). PMID 33630396 DOI: 10.1002/anie.202100810 |
0.632 |
|
| 2020 |
Cong F, Lv XY, Day CS, Martin R. Dual Catalytic Strategy for Forging spsp and spsp Architectures via βScission of Aliphatic Alcohol Derivatives. Journal of the American Chemical Society. PMID 33252234 DOI: 10.1021/jacs.0c11172 |
0.59 |
|
| 2020 |
Börjesson M, Janssen-Müller D, Sahoo B, Duan Y, Wang X, Martin R. Remote sp C-H Carboxylation via Catalytic 1,4-Ni Migration with CO. Journal of the American Chemical Society. PMID 32910658 DOI: 10.1021/Jacs.0C08810 |
0.795 |
|
| 2020 |
Somerville RJ, Odena C, Obst MF, Hazari N, Hopmann KH, Martin R. Ni(I)-Alkyl Complexes Bearing Phenanthroline Ligands: Experimental Evidence for CO Insertion at Ni(I) Centers. Journal of the American Chemical Society. PMID 32520556 DOI: 10.1021/Jacs.0C04695 |
0.438 |
|
| 2020 |
Martin R, Sun SZ, Duan Y, Mega RS, Somerville RJ. Site-Selective 1,2-Dicarbofunctionalization of Vinyl Boronates via Dual Catalysis. Angewandte Chemie (International Ed. in English). PMID 31910307 DOI: 10.1002/Anie.201916279 |
0.422 |
|
| 2020 |
Yanagi T, Somerville RJ, Nogi K, Martin R, Yorimitsu H. Ni-Catalyzed Carboxylation of C(sp2)–S Bonds with CO2: Evidence for the Multifaceted Role of Zn Acs Catalysis. 10: 2117-2123. DOI: 10.1021/Acscatal.9B05141 |
0.48 |
|
| 2020 |
Rand AW, Yin H, Xu L, Giacoboni J, Martin-Montero R, Romano C, Montgomery J, Martin R. Dual Catalytic Platform for Enabling sp3 α C–H Arylation and Alkylation of Benzamides Acs Catalysis. 10: 4671-4676. DOI: 10.1021/Acscatal.0C01318 |
0.424 |
|
| 2019 |
Somerville RJ, Hale LVA, Gómez-Bengoa E, Burés J, Martin R. Correction to "Intermediacy of Ni-Ni Species in sp C-O Bond Cleavage of Aryl Esters: Relevance in Catalytic C-Si Bond Formation". Journal of the American Chemical Society. PMID 31829627 DOI: 10.1021/Jacs.9B13098 |
0.41 |
|
| 2019 |
Martin R, Gu Y, Duan Y, Shen Y. Stereoselective Base-Catalyzed 1,1-Silaboration of Terminal Alkynes. Angewandte Chemie (International Ed. in English). PMID 31742879 DOI: 10.1002/Anie.201913544 |
0.402 |
|
| 2019 |
Sun SZ, Romano C, Martin R. Site-selective catalytic deaminative alkylation of unactivated olefins. Journal of the American Chemical Society. PMID 31565935 DOI: 10.1021/Jacs.9B07489 |
0.457 |
|
| 2019 |
Martin R, Sahoo B, Bellotti P, Juliá-Hernández F, Meng QY, Crespi S, König B. Site-Selective, Remote sp3 C-H Carboxylation Enabled by the Merger of Photoredox and Nickel Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31074058 DOI: 10.1002/Chem.201902095 |
0.743 |
|
| 2019 |
Martin-Montero R, Yatham VR, Yin H, Davies J, Martin R. Ni-catalyzed Reductive Deaminative Arylation at sp Carbon Centers. Organic Letters. PMID 30924663 DOI: 10.1021/Acs.Orglett.9B01016 |
0.493 |
|
| 2019 |
Tortajada A, Duan Y, Sahoo B, Cong F, Toupalas G, Sallustrau A, Loreau O, Audisio D, Martin R. Catalytic Decarboxylation/Carboxylation Platform for Accessing Isotopically Labeled Carboxylic Acids Acs Catalysis. 9: 5897-5901. DOI: 10.1021/Acscatal.9B01921 |
0.688 |
|
| 2019 |
Börjesson M, Tortajada A, Martin R. N-Containing Heterocycles on Demand by Merging Ni Catalysis and Photoredox PCET Chem. 5: 254-256. DOI: 10.1016/J.Chempr.2019.01.010 |
0.371 |
|
| 2019 |
Janssen‐Müller D, Sahoo B, Sun S, Martin R. Tackling Remote
sp
3
C−H Functionalization via Ni‐Catalyzed “chain‐walking” Reactions Israel Journal of Chemistry. 60: 195-206. DOI: 10.1002/Ijch.201900072 |
0.701 |
|
| 2018 |
Liu XW, Zarate C, Martin R. Base-Mediated Defluorosilylation of C(sp )-F and C(sp )-F Bonds. Angewandte Chemie (International Ed. in English). PMID 30575235 DOI: 10.1002/Anie.201813294 |
0.416 |
|
| 2018 |
Gu Y, Shen Y, Zarate C, Martin R. A Mild & Direct Site-Selective sp2 C-H Silylation of (Poly)Azines. Journal of the American Chemical Society. PMID 30562018 DOI: 10.1021/Jacs.8B12063 |
0.446 |
|
| 2018 |
Sun SZ, Börjesson M, Martin R, Martin R. Site-Selective Ni-Catalyzed Reductive Coupling of a-Haloboranes with Unactivated Olefins. Journal of the American Chemical Society. PMID 30244574 DOI: 10.1021/Jacs.8B09425 |
0.489 |
|
| 2018 |
Shen Y, Gu Y, Martin R. sp3 C-H Arylation and Alkylation Enabled by the Synergy of Triplet Excited Ketones and Nickel Catalysts. Journal of the American Chemical Society. PMID 30184423 DOI: 10.1021/Jacs.8B07405 |
0.466 |
|
| 2018 |
Somerville R, Hale LVA, Gomez-Bengoa E, Burés J, Martin R. Intermediacy of Ni-Ni species in sp2 C-O bond cleavage of aryl esters: relevance in catalytic C-Si Bond Formation. Journal of the American Chemical Society. PMID 29909614 DOI: 10.1021/Jacs.8B04479 |
0.456 |
|
| 2018 |
Martin R, Tortajada A, Juliá-Hernández F, Borjesson M, Moragas T. Transition metal-catalyzed carboxylation reactions with carbon dioxide. Angewandte Chemie (International Ed. in English). PMID 29722461 DOI: 10.1002/Anie.201803186 |
0.45 |
|
| 2018 |
Sommer H, Juliá-Hernández F, Martin R, Marek I. Walking Metals for Remote Functionalization. Acs Central Science. 4: 153-165. PMID 29532015 DOI: 10.1021/Acscentsci.8B00005 |
0.37 |
|
| 2018 |
Martin R, Sun SZ. Ni-catalyzed Umpolung Arylation of Ambiphilic a-Bromo Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 29446875 DOI: 10.1002/Anie.201712428 |
0.498 |
|
| 2018 |
Martin R, Tortajada Navarro A, Ninokata R. Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2. Journal of the American Chemical Society. PMID 29376353 DOI: 10.1021/Jacs.7B13220 |
0.397 |
|
| 2017 |
Gaydou M, Moragas T, Julia-Hernandez F, Martin R. Site-Selective Catalytic Carboxylation of Unsaturated Hydrocarbons with CO2 and Water. Journal of the American Chemical Society. PMID 28814076 DOI: 10.1021/Jacs.7B07637 |
0.364 |
|
| 2017 |
Martin R, Reddy Yatham V, Shen Y. Catalytic intermolecular dicarbofunctionalization of styrenes with CO2 and radical precursors. Angewandte Chemie (International Ed. in English). PMID 28700104 DOI: 10.1002/Anie.201706263 |
0.439 |
|
| 2017 |
Shimomaki K, Murata K, Martin R, Iwasawa N. Visible Light-Driven Carboxylation of Aryl Halides by the Combined Use of Palladium and Photoredox Catalysts. Journal of the American Chemical Society. PMID 28657743 DOI: 10.1021/Jacs.7B04838 |
0.407 |
|
| 2017 |
Juliá-Hernández F, Moragas T, Cornella J, Martin R. Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide. Nature. 545: 84-88. PMID 28470192 DOI: 10.1038/Nature22316 |
0.466 |
|
| 2017 |
Somerville RJ, Martin R. Forging C-C Bonds Through Decarbonylation of Aryl Ketones. Angewandte Chemie (International Ed. in English). PMID 28466981 DOI: 10.1002/Anie.201702188 |
0.39 |
|
| 2017 |
van Gemmeren M, Börjesson M, Tortajada A, Sun SZ, Okura K, Martin R. Switchable Site-Selective Catalytic Carboxylation of Allylic Alcohols with CO2. Angewandte Chemie (International Ed. in English). PMID 28464503 DOI: 10.1002/Anie.201702857 |
0.745 |
|
| 2017 |
Márquez IR, Fuentes N, Cruz CM, Puente-Muñoz V, Sotorrios L, Marcos ML, Choquesillo-Lazarte D, Biel B, Crovetto L, Gómez-Bengoa E, González MT, Martin R, Cuerva JM, Campaña AG. Versatile synthesis and enlargement of functionalized distorted heptagon-containing nanographenes. Chemical Science. 8: 1068-1074. PMID 28451246 DOI: 10.1039/C6Sc02895K |
0.367 |
|
| 2017 |
Gu Y, Martín R. Ni-Catalyzed Stannylation of Aryl Esters via C-O Bond Cleavage. Angewandte Chemie (International Ed. in English). PMID 28185372 DOI: 10.1002/Anie.201611720 |
0.449 |
|
| 2017 |
Martin-Montero R, Krolikowski T, Zarate C, Manzano R, Martin R. Stereospecific Nickel-Catalyzed Borylation of Secondary Benzyl Pivalates Synlett. 28: 2604-2608. DOI: 10.1055/S-0036-1590962 |
0.474 |
|
| 2017 |
Somerville RJ, Martin R. Bildung von C-C-Bindungen durch Decarbonylierung von Arylketonen Angewandte Chemie. 129: 6810-6812. DOI: 10.1002/Ange.201702188 |
0.311 |
|
| 2016 |
Zarate C, Nakajima M, Martin R. A Mild & Ligand-Free Ni-catalyzed Silylation via C-OMe Cleavage. Journal of the American Chemical Society. PMID 28030761 DOI: 10.1021/Jacs.6B10998 |
0.486 |
|
| 2016 |
Wang X, Nakajima M, Serrano E, Martin R. Alkyl Bromides as Mild Hydride Sources in Ni-Catalyzed Hydroamidation of Alkynes with Isocyanates. Journal of the American Chemical Society. 138: 15531-15534. PMID 27934006 DOI: 10.1021/Jacs.6B10351 |
0.703 |
|
| 2016 |
Börjesson M, Moragas T, Gallego D, Martin R. Metal-Catalyzed Carboxylation of Organic (Pseudo)halides with CO2. Acs Catalysis. 6: 6739-6749. PMID 27747133 DOI: 10.1021/Acscatal.6B02124 |
0.427 |
|
| 2016 |
Juliá-Hernández F, Gaydou M, Serrano E, van Gemmeren M, Martin R. Ni- and Fe-catalyzed Carboxylation of Unsaturated Hydrocarbons with CO2. Topics in Current Chemistry (Journal). 374: 45. PMID 27573397 DOI: 10.1007/S41061-016-0045-Z |
0.731 |
|
| 2016 |
Serrano E, Martin R. Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides. Angewandte Chemie (International Ed. in English). PMID 27357076 DOI: 10.1002/Anie.201605162 |
0.463 |
|
| 2016 |
Börjesson M, Moragas T, Martin R. Ni-catalyzed Carboxylation of Unactivated Alkyl Chlorides with CO2. Journal of the American Chemical Society. PMID 27269443 DOI: 10.1021/Jacs.6B04088 |
0.406 |
|
| 2016 |
Gutiérrez-Bonet Á, Juliá-Hernández F, de Luis B, Martin R. Pd-Catalyzed C(sp(3))-H Functionalization/Carbenoid Insertion: All-Carbon Quaternary Centers via Multiple C-C Bond Formation. Journal of the American Chemical Society. PMID 27145029 DOI: 10.1021/Jacs.6B02867 |
0.435 |
|
| 2016 |
Moragas T, Gaydou M, Martin R. Nickel-Catalyzed Carboxylation of Benzylic C-N Bonds with CO2. Angewandte Chemie (International Ed. in English). 55: 5053-7. PMID 26991022 DOI: 10.1002/Anie.201600697 |
0.453 |
|
| 2016 |
Moragas T, Martin R. Nickel-Catalyzed Reductive Carboxylation of Cyclopropyl Motifs with Carbon Dioxide Synthesis. 48: 2816-2822. DOI: 10.1055/S-0035-1560439 |
0.394 |
|
| 2016 |
Zarate C, Gemmeren Mv, Somerville RJ, Martin R. Phenol Derivatives: Modern Electrophiles in Cross-Coupling Reactions Advances in Organometallic Chemistry. 66: 143-222. DOI: 10.1016/Bs.Adomc.2016.07.001 |
0.418 |
|
| 2016 |
Serrano E, Martin R. Back Cover: Nickel‐Catalyzed Reductive Amidation of Unactivated Alkyl Bromides (Angew. Chem. Int. Ed. 37/2016) Angewandte Chemie. 55: 11302-11302. DOI: 10.1002/Anie.201606539 |
0.375 |
|
| 2016 |
Serrano E, Martin R. Rücktitelbild: Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides (Angew. Chem. 37/2016) Angewandte Chemie. 128: 11472-11472. DOI: 10.1002/Ange.201606539 |
0.486 |
|
| 2015 |
Liu XW, Echavarren J, Zárate C, Martin R. Ni-catalyzed borylation of aryl fluorides via C-F cleavage. Journal of the American Chemical Society. PMID 26397717 DOI: 10.1021/Jacs.5B08103 |
0.358 |
|
| 2015 |
Wang X, Nakajima M, Martin R. Ni-catalyzed Regioselective Hydrocarboxylation of Alkynes with CO2 by Using Simple Alcohols as Proton Sources. Journal of the American Chemical Society. PMID 26130587 DOI: 10.1021/Jacs.5B05513 |
0.683 |
|
| 2015 |
Juliá-Hernández F, Ziadi A, Nishimura A, Martin R. Nickel-catalyzed Chemo-, Regio- and Diastereoselective Bond Formation through Proximal CC Cleavage of Benzocyclobutenones. Angewandte Chemie (International Ed. in English). PMID 26096718 DOI: 10.1002/Anie.201503461 |
0.428 |
|
| 2015 |
Zarate C, Manzano R, Martin R. Ipso-Borylation of Aryl Ethers via Ni-Catalyzed C-OMe Cleavage. Journal of the American Chemical Society. 137: 6754-7. PMID 25978094 DOI: 10.1021/Jacs.5B03955 |
0.506 |
|
| 2015 |
Wang X, Liu Y, Martin R. Ni-Catalyzed Divergent Cyclization/Carboxylation of Unactivated Primary and Secondary Alkyl Halides with CO2. Journal of the American Chemical Society. 137: 6476-9. PMID 25968409 DOI: 10.1021/Jacs.5B03340 |
0.715 |
|
| 2015 |
Cornella J, Jackson EP, Martin R. Nickel-catalyzed enantioselective C-C bond formation through C(sp2)-O cleavage in aryl esters. Angewandte Chemie (International Ed. in English). 54: 4075-8. PMID 25650559 DOI: 10.1002/Anie.201412051 |
0.461 |
|
| 2014 |
Moragas T, Cornella J, Martin R. Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2. Journal of the American Chemical Society. 136: 17702-5. PMID 25473825 DOI: 10.1021/Ja509077A |
0.421 |
|
| 2014 |
Cornella J, Zarate C, Martin R. Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity. Chemical Society Reviews. 43: 8081-97. PMID 25157613 DOI: 10.1039/C4Cs00206G |
0.398 |
|
| 2014 |
Wang X, Gallardo-Donaire J, Martin R. Mild ArI-catalyzed C(sp²)-H or C(sp³)-H functionalization/C-O formation: an intriguing catalyst-controlled selectivity switch. Angewandte Chemie (International Ed. in English). 53: 11084-7. PMID 25156610 DOI: 10.1002/Anie.201407011 |
0.712 |
|
| 2014 |
Liu Y, Cornella J, Martin R. Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2. Journal of the American Chemical Society. 136: 11212-5. PMID 25068174 DOI: 10.1021/Ja5064586 |
0.411 |
|
| 2014 |
Moragas T, Correa A, Martin R. Metal-catalyzed reductive coupling reactions of organic halides with carbonyl-type compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 8242-58. PMID 24905555 DOI: 10.1002/Chem.201402509 |
0.373 |
|
| 2014 |
Correa A, Martin R. Ni-catalyzed direct reductive amidation via C-O bond cleavage. Journal of the American Chemical Society. 136: 7253-6. PMID 24791834 DOI: 10.1021/Ja5029793 |
0.505 |
|
| 2014 |
Zarate C, Martin R. A mild Ni/Cu-catalyzed silylation via C-O cleavage. Journal of the American Chemical Society. 136: 2236-9. PMID 24476124 DOI: 10.1021/Ja412107B |
0.424 |
|
| 2014 |
Correa A, León T, Martin R. Ni-catalyzed carboxylation of C(sp2)- and C(sp3)-O bonds with CO2. Journal of the American Chemical Society. 136: 1062-9. PMID 24377699 DOI: 10.1021/Ja410883P |
0.498 |
|
| 2014 |
Cornella J, Zarate C, Martin R. Ni‐catalyzed Reductive Cleavage of Methyl 3‐Methoxy‐2‐Naphthoate Organic Syntheses. 91: 260-272. DOI: 10.1002/0471264229.Os091.23 |
0.401 |
|
| 2014 |
Martin R, Flores‐Gaspar A. Synthesis of 8,8‐Dipropylbicyclo[4.2.0]octa‐1,3,5‐trien‐7‐one via Pd‐catalyzed Intramolecular CH Bond‐Acylation Organic Syntheses. 159-169. DOI: 10.1002/0471264229.Os089.17 |
0.356 |
|
| 2013 |
Cornella J, Martin R. Ni-catalyzed stereoselective arylation of inert C-O bonds at low temperatures. Organic Letters. 15: 6298-301. PMID 24252127 DOI: 10.1021/Ol4031815 |
0.392 |
|
| 2013 |
Gutiérrez-Bonet Á, Flores-Gaspar A, Martin R. Fe-catalyzed regiodivergent [1,2]-shift of α-aryl aldehydes. Journal of the American Chemical Society. 135: 12576-9. PMID 23927556 DOI: 10.1021/Ja4068707 |
0.379 |
|
| 2013 |
De La Fuente A, Martin R, Mena-Barragán T, Verdaguer X, García Fernández JM, Ortiz Mellet C, Riera A. Stereoselective synthesis of 2-acetamido-1,2-dideoxyallonojirimycin (DAJNAc), a new potent hexosaminidase inhibitor Organic Letters. 15: 3638-3641. PMID 23802126 DOI: 10.1021/Ol401517X |
0.529 |
|
| 2013 |
Gallardo-Donaire J, Martin R. Cu-catalyzed mild C(sp2)-H functionalization assisted by carboxylic acids en route to hydroxylated arenes. Journal of the American Chemical Society. 135: 9350-3. PMID 23758209 DOI: 10.1021/Ja4047894 |
0.462 |
|
| 2013 |
Cornella J, Gómez-Bengoa E, Martin R. Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates. Journal of the American Chemical Society. 135: 1997-2009. PMID 23316793 DOI: 10.1021/Ja311940S |
0.454 |
|
| 2013 |
León T, Correa A, Martin R. Ni-catalyzed direct carboxylation of benzyl halides with CO2. Journal of the American Chemical Society. 135: 1221-4. PMID 23301781 DOI: 10.1021/Ja311045F |
0.442 |
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| 2013 |
Correa A, Cornella J, Martin R. Nickel-catalyzed decarbonylative C-H coupling reactions: a strategy for preparing bis(heteroaryl) backbones. Angewandte Chemie (International Ed. in English). 52: 1878-80. PMID 23288859 DOI: 10.1002/Anie.201208843 |
0.433 |
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| 2013 |
Ziadi A, Correa A, Martin R. Formal γ-alkynylation of ketones via Pd-catalyzed C-C cleavage. Chemical Communications (Cambridge, England). 49: 4286-8. PMID 23135385 DOI: 10.1039/C2Cc37281A |
0.395 |
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| 2013 |
Flores-Gaspar A, Martin R. Recent Advances in the Synthesis and Application of Benzocyclobutenones and Related Compounds Synthesis. 45: 563-580. DOI: 10.1055/S-0032-1316850 |
0.422 |
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| 2013 |
Correa A, Cornella J, Martin R. Nickel-katalysierte decarbonylierende C-H-Kupplungen: eine Strategie zur Synthese von Bis(heteroaryl)-Strukturen Angewandte Chemie. 125: 1928-1930. DOI: 10.1002/Ange.201208843 |
0.371 |
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| 2012 |
Flores-Gaspar A, Gutiérrez-Bonet Á, Martin R. N-Heterocyclic carbene dichotomy in Pd-catalyzed acylation of aryl chlorides via C-H bond functionalization. Organic Letters. 14: 5234-7. PMID 23030460 DOI: 10.1021/Ol3023819 |
0.433 |
|
| 2012 |
Ziadi A, Martin R. Ligand-accelerated Pd-catalyzed ketone γ-arylation via C-C cleavage with aryl chlorides. Organic Letters. 14: 1266-9. PMID 22332797 DOI: 10.1021/Ol300119U |
0.455 |
|
| 2012 |
Barbero N, Martin R. Ligand-free Ni-catalyzed reductive cleavage of inert carbon-sulfur bonds. Organic Letters. 14: 796-9. PMID 22256952 DOI: 10.1021/Ol2033306 |
0.486 |
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| 2011 |
Novák P, Correa A, Gallardo-Donaire J, Martin R. Synergistic palladium-catalyzed C(sp3)-H activation/C(sp3)-O bond formation: a direct, step-economical route to benzolactones. Angewandte Chemie (International Ed. in English). 50: 12236-9. PMID 22038700 DOI: 10.1002/Anie.201105894 |
0.463 |
|
| 2011 |
Flores‐Gaspar A, Martin R. Mechanistic Switch via Subtle Ligand Modulation: Palladium-Catalyzed Synthesis of α,β-Substituted Styrenes via CH Bond Functionalization Advanced Synthesis & Catalysis. 353: 1223-1228. DOI: 10.1002/Adsc.201100140 |
0.424 |
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| 2010 |
Álvarez-Bercedo P, Martin R. Ni-catalyzed reduction of inert C-O bonds: a new strategy for using aryl ethers as easily removable directing groups. Journal of the American Chemical Society. 132: 17352-3. PMID 20843037 DOI: 10.1021/Ja106943Q |
0.457 |
|
| 2010 |
Alvarez-Bercedo P, Flores-Gaspar A, Correa A, Martin R. Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: a highly efficient synthesis of benzocyclobutenones. Journal of the American Chemical Society. 132: 466-7. PMID 20038097 DOI: 10.1021/Ja909811T |
0.471 |
|
| 2009 |
Correa A, Martín R. Palladium-catalyzed direct carboxylation of aryl bromides with carbon dioxide. Journal of the American Chemical Society. 131: 15974-5. PMID 19886688 DOI: 10.1021/Ja905264A |
0.467 |
|
| 2009 |
Correa A, Martín R. Metal-catalyzed carboxylation of organometallic reagents with carbon dioxide. Angewandte Chemie (International Ed. in English). 48: 6201-4. PMID 19544522 DOI: 10.1002/Anie.200900667 |
0.317 |
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| 2008 |
Martín R, Buchwald SL. An improved protocol for the Pd-catalyzed alpha-arylation of aldehydes with aryl halides. Organic Letters. 10: 4561-4. PMID 18808127 DOI: 10.1021/Ol8017775 |
0.605 |
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| 2008 |
Martin R, Buchwald SL. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Accounts of Chemical Research. 41: 1461-73. PMID 18620434 DOI: 10.1021/Ar800036S |
0.638 |
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| 2008 |
Fürstner A, Martin R, Krause H, Seidel G, Goddard R, Lehmann CW. Preparation, structure, and reactivity of nonstabilized organoiron compounds. Implications for iron-catalyzed cross coupling reactions. Journal of the American Chemical Society. 130: 8773-87. PMID 18597432 DOI: 10.1021/Ja801466T |
0.526 |
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| 2008 |
Fürstner A, Majima K, Martín R, Krause H, Kattnig E, Goddard R, Lehmann CW. A cheap metal for a "noble" task: preparative and mechanistic aspects of cycloisomerization and cycloaddition reactions catalyzed by low-valent iron complexes. Journal of the American Chemical Society. 130: 1992-2004. PMID 18197669 DOI: 10.1021/Ja0777180 |
0.552 |
|
| 2007 |
Martín R, Cuenca A, Buchwald SL. Sequential copper-catalyzed vinylation/cyclization: an efficient synthesis of functionalized oxazoles. Organic Letters. 9: 5521-4. PMID 18020351 DOI: 10.1021/Ol7024718 |
0.634 |
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| 2007 |
Martín R, Buchwald SL. A general method for the direct alpha-arylation of aldehydes with aryl bromides and chlorides. Angewandte Chemie (International Ed. in English). 46: 7236-9. PMID 17722128 DOI: 10.1002/Anie.200703009 |
0.561 |
|
| 2007 |
Martín R, Larsen CH, Cuenca A, Buchwald SL. Cu-catalyzed tandem C-N bond formation for the synthesis of pyrroles and heteroarylpyrroles. Organic Letters. 9: 3379-82. PMID 17655316 DOI: 10.1021/Ol7014225 |
0.79 |
|
| 2007 |
Martin R, Buchwald SL. Pd-catalyzed Kumada-Corriu cross-coupling reactions at low temperatures allow the use of Knochel-type Grignard reagents. Journal of the American Chemical Society. 129: 3844-5. PMID 17352483 DOI: 10.1021/Ja070830D |
0.606 |
|
| 2006 |
Martín R, Rodríguez Rivero M, Buchwald SL. Domino cu-catalyzed C--N coupling/hydroamidation: a highly efficient synthesis of nitrogen heterocycles. Angewandte Chemie (International Ed. in English). 45: 7079-82. PMID 17009380 DOI: 10.1002/Anie.200602917 |
0.622 |
|
| 2005 |
Fürstner A, Martin R, Majima K. Cycloisomerization of enynes catalyzed by iron(0)-ate complexes. Journal of the American Chemical Society. 127: 12236-7. PMID 16131197 DOI: 10.1021/Ja0532739 |
0.561 |
|
| 2005 |
Martín R, Murruzzu C, Pericàs MA, Riera A. General approach to glycosidase inhibitors. Enantioselective synthesis of deoxymannojirimycin and swainsonine. The Journal of Organic Chemistry. 70: 2325-8. PMID 15760222 DOI: 10.1021/Jo048172S |
0.68 |
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| 2005 |
Fürstner A, Martin R. Advances in iron catalyzed cross coupling reactions Chemistry Letters. 34: 624-629. DOI: 10.1246/Cl.2005.624 |
0.502 |
|
| 2004 |
Martin R, Fürstner A. Cross-coupling of alkyl halides with aryl grignard reagents catalyzed by a low-valent iron complex. Angewandte Chemie (International Ed. in English). 43: 3955-7. PMID 15274224 DOI: 10.1002/Anie.200460504 |
0.517 |
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| 2002 |
Martín R, Alcón M, Pericàs MA, Riera A. Ring-closing metathesis of chiral allylamines. Enantioselective synthesis of (2S,3R,4S)-3,4-dihydroxyproline. The Journal of Organic Chemistry. 67: 6896-901. PMID 12353980 DOI: 10.1021/Jo025832P |
0.6 |
|
| 2000 |
Martín R, Moyano A, Pericàs MA, Riera A. A concise enantioselective entry to the synthesis of deoxy-azasugars Organic Letters. 2: 93-95. PMID 10814254 DOI: 10.1021/Ol991280U |
0.674 |
|
| 2000 |
Martín R, Romea P, Tey C, Urpí F, Vilarrasa J. Simple and Efficient Preparation of Ketones from Morpholine Amides Synlett. 12: 1414-1416. DOI: 10.1055/S-1997-1050 |
0.353 |
|
| 1997 |
Figueras S, Martín R, Romea P, Urpí F, Vilarrasa J. Highly stereoselective aldol reactions of titanium enolates from ethyl α-silyloxyalkyl ketones Tetrahedron Letters. 38: 1637-1640. DOI: 10.1016/S0040-4039(97)00108-1 |
0.349 |
|
| 1997 |
Martín R, Pascual O, Romea P, Rovira R, Urpí F, Vilarrasa J. A simple procedure for the preparation of enantiopure ethyl α-hydroxyalkyl ketones Tetrahedron Letters. 38: 1633-1636. DOI: 10.1016/S0040-4039(97)00107-X |
0.311 |
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