| Year |
Citation |
Score |
| 2024 |
Miller L, Bauer F, Breit B. A Tandem Hydroformylation-organocatalyzed Friedel-Crafts reaction for the synthesis of Diindolylmethanes. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400188. PMID 38411034 DOI: 10.1002/chem.202400188 |
0.357 |
|
| 2023 |
Miller L, Impelmann A, Bauer F, Breit B. Carbonylation as a Key Step in New Tandem Reactions - A Route to BODIPYs. Chemistry (Weinheim An Der Bergstrasse, Germany). e202303752. PMID 38109037 DOI: 10.1002/chem.202303752 |
0.368 |
|
| 2023 |
Panahi F, Bauer F, Breit B. Rhodium-Catalyzed Allylic Addition as an Atom-Efficient Approach in Total Synthesis. Accounts of Chemical Research. 56: 3676-3693. PMID 38064346 DOI: 10.1021/acs.accounts.3c00322 |
0.366 |
|
| 2023 |
Tang N, Zachmann RJ, Xie H, Zheng J, Breit B. Visible-light induced metal-free intramolecular reductive cyclisations of ketones with alkynes and allenes. Chemical Communications (Cambridge, England). PMID 36723349 DOI: 10.1039/d2cc06972e |
0.432 |
|
| 2022 |
Zheng J, Breit B, Tang N, Xie H. Regio-, Diastereo-, and Enantioselective Decarboxylative Hydroaminoalkylation of Dienol Ethers Enabled by Dual Palladum/Photoredox Catalysis. Angewandte Chemie (International Ed. in English). PMID 35170841 DOI: 10.1002/anie.202200105 |
0.456 |
|
| 2021 |
Geissler AGA, Riesterer JR, Breit B. Stereodivergent Palladium- and Rhodium-Catalyzed Intramolecular Addition of Tosylureas to Allenes: Diastereoselective Synthesis of Tetrahydropyrimidinones. Organic Letters. 23: 9168-9172. PMID 34806888 DOI: 10.1021/acs.orglett.1c03482 |
0.402 |
|
| 2021 |
Becker A, Grugel CP, Breit B. Rhodium-Catalyzed Stereoselective Cyclization of 3-Allenylindoles and -Allenyltryptamines to Functionalized Vinylic Spiroindolenines. Organic Letters. PMID 33900096 DOI: 10.1021/acs.orglett.1c01234 |
0.33 |
|
| 2021 |
Nikbakht A, Amiri K, Khosravi H, Zhou Y, Balalaie S, Breit B. Copper-Catalyzed Cycloisomerization of Unactivated Allene-Tethered -Propargyl Oximes: A Domino Reaction Sequence toward the Synthesis of Hexahydropyrrolo[3,4-]azepin-5(4)-ones. Organic Letters. PMID 33843238 DOI: 10.1021/acs.orglett.1c00837 |
0.341 |
|
| 2020 |
Breit B, Maurer D. Urea-substituted Tetramethylcyclopentadienyl Ligands for Supramolecularly Accelerated Rh(III)-catalyzed ortho-C-H Olefination of Benzoic Acid Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33294985 DOI: 10.1002/chem.202005130 |
0.324 |
|
| 2020 |
Breit B, Schmidt J. Rhodium-Catalyzed Cyclisation of Terminal and Internal Allenols: An Atom Economic and Highly Stereoselective Access Towards Tetrahydropyrans Johannes P. Schmidt, Bernhard Breit. Angewandte Chemie (International Ed. in English). PMID 32940396 DOI: 10.1002/Anie.202009166 |
0.423 |
|
| 2020 |
Breit B, Lutterbeck M, Liebich A, Keller M, Herp D, Vogelmann A, Jung M, Brosowsky J. Syntheses of Thailandepsin B Pseudo-Natural Products: Access to new highly potent HDAC Inhibitors via Late Stage Modification. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32725698 DOI: 10.1002/Chem.202002449 |
0.38 |
|
| 2020 |
Hosseini-Eshbala F, Sedrpoushan A, Breit B, Mohanazadeh F, Veisi H. Ionic-liquid-modified CMK-3 as a support for the immobilization of molybdate ions (MoO): Heterogeneous nanocatalyst for selective oxidation of sulfides and benzylic alcohols. Materials Science & Engineering. C, Materials For Biological Applications. 110: 110577. PMID 32204056 DOI: 10.1016/J.Msec.2019.110577 |
0.346 |
|
| 2020 |
Berthold D, Breit B. Total Syntheses of Cylindrocyclophanes Exemplifying the Power of Transition-Metal Catalysis in Natural-Product Synthesis Synlett. DOI: 10.1055/S-0040-1707144 |
0.364 |
|
| 2020 |
Halimehjani AZ, Khalesi M, Breit B. Amino Acid‐Based Dithiocarbamates as Efficient Intermediates for Diversity‐Oriented Synthesis of Thiazoles European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.202001050 |
0.392 |
|
| 2019 |
Berthold D, Klett J, Breit B. Rhodium-catalyzed asymmetric intramolecular hydroarylation of allenes: access to functionalized benzocycles. Chemical Science. 10: 10048-10052. PMID 32015818 DOI: 10.1039/C9Sc03894A |
0.464 |
|
| 2019 |
Berthold D, Breit B. Asymmetric Total Syntheses of (-)-Angustureine and (-)-Cuspareine via Rhodium-Catalyzed Hydroamination. Organic Letters. PMID 31877052 DOI: 10.1021/Acs.Orglett.9B04334 |
0.481 |
|
| 2019 |
Sergeieva T, Hamlin TA, Okovytyy S, Breit B, Bickelhaupt FM. Ligand-Mediated Regioselective Rhodium Catalyzed Benzotriazole-Allene Coupling: Mechanistic Exploration and Quantum Chemical Analysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31778591 DOI: 10.1002/Chem.201905359 |
0.346 |
|
| 2019 |
Grugel CP, Breit B. Rhodium-Catalyzed Diastereo- and Enantioselective Tandem Spirocyclization/Reduction of 3-Allenylindoles: Access to Functionalized Vinylic Spiroindolines. Organic Letters. 21: 9672-9676. PMID 31769696 DOI: 10.1021/Acs.Orglett.9B03835 |
0.458 |
|
| 2019 |
Fang W, Bauer F, Dong Y, Breit B. A domino reaction for generating β-aryl aldehydes from alkynes by substrate recognition catalysis. Nature Communications. 10: 4868. PMID 31653836 DOI: 10.1038/S41467-019-12770-W |
0.471 |
|
| 2019 |
Breit B, González M. Visible-Light-Driven Intermolecular Reductive Ene-Yne Coupling via Iridium/Coblat Dual Catalysis for C(sp3)-C(sp2) Bond Formation. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31549749 DOI: 10.1002/Chem.201903708 |
0.326 |
|
| 2019 |
Nikbakht A, Balalaie S, Breit B. Synthesis of 2-(Isoquinolin-1-yl)prop-2-en-1-ones via Silver(I)-Catalyzed One-Pot Tandem Reaction of -Alkynylbenzaldoximes with Propargylic Alcohols. Organic Letters. PMID 31498640 DOI: 10.1021/Acs.Orglett.9B02952 |
0.407 |
|
| 2019 |
Hosseini-Eshbala F, Sedrpoushan A, Dehdashti MN, Breit B, Mohanazadeh F, Veisi H. Needle ball-like nanostructured mixed Cu-Ni-Co oxides: Synthesis, characterization and application to the selective oxidation of sulfides to sulfoxides. Materials Science & Engineering. C, Materials For Biological Applications. 103: 109814. PMID 31349404 DOI: 10.1016/J.Msec.2019.109814 |
0.307 |
|
| 2019 |
Wang YH, Breit B. Chemo-, regio-, and enantioselective synthesis of allylic nitrones via rhodium-catalyzed addition of oximes to allenes. Chemical Communications (Cambridge, England). PMID 31192322 DOI: 10.1039/C9Cc03391B |
0.476 |
|
| 2019 |
Zhou Y, Nikbakht A, Bauer F, Breit B. A rhodium catalyzed cycloisomerization and tandem Diels-Alder reaction for facile access to diverse bicyclic and tricyclic heterocycles. Chemical Science. 10: 4805-4810. PMID 31183033 DOI: 10.1039/C9Sc00980A |
0.46 |
|
| 2019 |
Grugel CP, Breit B. Rhodium-Catalyzed Enantioselective Cyclization of 3-Allenyl-indoles: Access to Functionalized Tetrahydrocarbazoles. Organic Letters. PMID 31136189 DOI: 10.1021/Acs.Orglett.9B01721 |
0.458 |
|
| 2019 |
Breit B, Hilpert L. Rhodium-Catalyzed Parallel Kinetic Resolution of Racemic Internal Allenes Towards Enantiopure Allylic 1,3-Diketones. Angewandte Chemie (International Ed. in English). PMID 31106496 DOI: 10.1002/Anie.201903365 |
0.428 |
|
| 2019 |
Breit B, Berthold D, Geissler A, Giofré S. Rhodium-Catalyzed Asymmetric Intramolecular Hydroamination of Allenes. Angewandte Chemie (International Ed. in English). PMID 31090994 DOI: 10.1002/Anie.201904833 |
0.451 |
|
| 2019 |
Schmidt JP, Breit B. Transition metal catalyzed stereodivergent synthesis of - and -δ-vinyl-lactams: formal total synthesis of (-)-cermizine C and (-)-senepodine G. Chemical Science. 10: 3074-3079. PMID 30996889 DOI: 10.1039/C8Sc05502E |
0.443 |
|
| 2019 |
Breit B, Steib P. Concise Total Synthesis of (-)-Vermiculine through a Rhodium-Catalyzed C2-symmetric Dimerization Strategy. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30672028 DOI: 10.1002/Chem.201900216 |
0.418 |
|
| 2019 |
Ziyaei Halimehjani A, Breit B. Catalyst-free hydrothiolation of alkynes with dithiocarbamic acids. Chemical Communications (Cambridge, England). 55: 1253-1255. PMID 30632570 DOI: 10.1039/C8Cc09726G |
0.448 |
|
| 2019 |
Breit B, Zheng J. Regiodivergent Hydroaminoalkylation of Alkynes and Allenes via a Combined Rhodium and Photoredox Catalytic System. Angewandte Chemie (International Ed. in English). PMID 30620131 DOI: 10.1002/Anie.201813646 |
0.476 |
|
| 2019 |
Zheng J, Wörl B, Breit B. Rhodium-Catalyzed Chemo-, Regio-, and Enantioselective Allylation of 2-Aminothiazoles with Terminal Allenes European Journal of Organic Chemistry. 2019: 5180-5182. DOI: 10.1002/Ejoc.201900435 |
0.47 |
|
| 2018 |
Zheng J, Hosseini-Eshbala F, Dong YX, Breit B. Palladium-catalyzed trisallylation of benzoxazoles and 2-aryl-1,3,4-oxadiazoles with alkyne. Chemical Communications (Cambridge, England). PMID 30547170 DOI: 10.1039/C8Cc09165J |
0.349 |
|
| 2018 |
Breit B, Hilpert L, Sieger S, Haydl A. Palladium- and Rhodium-Catalyzed Dynamic Kinetic Resolution of Racemic Internal Allenes Towards Chiral Pyrazoles. Angewandte Chemie (International Ed. in English). PMID 30536499 DOI: 10.1002/Anie.201812984 |
0.783 |
|
| 2018 |
Breit B, Fang W. Tandem Regioselective Hydroformylation-Hydrogenation of Internal Alkynes employing a Supramolecular Catalyst. Angewandte Chemie (International Ed. in English). PMID 30216612 DOI: 10.1002/Anie.201809073 |
0.424 |
|
| 2018 |
Breit B, Berthold D. Total Synthesis of (-)-Cylindrocyclophane F: A Yardstick for Probing New Catalytic C-C Bond Forming Methodologies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30204273 DOI: 10.1002/Chem.201804585 |
0.401 |
|
| 2018 |
Breit B, Grugel C. Rhodium-catalyzed Asymmetric Allylation of Malononitriles as Masked Acyl Cyanide with Allenes: Efficient Access to β,ɣ-unsaturated Carbonyls. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30113106 DOI: 10.1002/Chem.201804150 |
0.43 |
|
| 2018 |
Spreider PA, Breit B. Palladium-Catalyzed Stereoselective Cyclization of in Situ Formed Allenyl Hemiacetals: Synthesis of Rosuvastatin and Pitavastatin. Organic Letters. PMID 29771125 DOI: 10.1021/Acs.Orglett.8B01156 |
0.491 |
|
| 2018 |
Breit B, Steib P. Enantioselective Rhodium-Catalyzed Dimerization of ω-Allenyl Carboxylic Acids: Straightforward Synthesis of C2-Symmetric Macrodiolides. Angewandte Chemie (International Ed. in English). PMID 29673025 DOI: 10.1002/Anie.201803369 |
0.483 |
|
| 2018 |
Zheng J, Breit B. Palladium-Catalyzed Direct C-H Allylation of Electron-Deficient Polyfluoroarenes with Alkynes. Organic Letters. PMID 29537272 DOI: 10.1021/Acs.Orglett.8B00393 |
0.406 |
|
| 2018 |
Breit B, Wenz KM. Inducing Axial-Chirality in a Supramolecular Catalyst. Angewandte Chemie (International Ed. in English). PMID 29508929 DOI: 10.1002/Anie.201801048 |
0.401 |
|
| 2018 |
Grugel CP, Breit B. Rhodium-Catalyzed Enantioselective Decarboxylative Alkynylation of Allenes with Arylpropiolic Acids. Organic Letters. PMID 29400478 DOI: 10.1021/Acs.Orglett.7B04035 |
0.433 |
|
| 2018 |
Warnke M, Jung T, Jacoby C, Agne M, Feller FM, Philipp B, Seiche W, Breit B, Boll M. Functional characterization of three specific acyl-coenzyme A synthetases involved in anaerobic cholesterol degradation in Sterolibacterium denitrificans Chol1S. Applied and Environmental Microbiology. PMID 29374035 DOI: 10.1128/Aem.02721-17 |
0.329 |
|
| 2018 |
Berthold D, Breit B. Chemo-, Regio-, and Enantioselective Rhodium-Catalyzed Allylation of Triazoles with Internal Alkynes and Terminal Allenes. Organic Letters. PMID 29350041 DOI: 10.1021/Acs.Orglett.7B03708 |
0.477 |
|
| 2018 |
Liu Z, Breit B. Rhodium-Catalyzed Regio- and Enantioselective Addition of N-Hydroxyphthalimide to Allenes: A Strategy To Synthesize Chiral Allylic Alcohols. Organic Letters. 20: 300-303. PMID 29280635 DOI: 10.1021/Acs.Orglett.7B03709 |
0.452 |
|
| 2018 |
Wenz KM, Leonhardt-Lutterbeck G, Breit B. Cover Picture: Inducing Axial Chirality in a Supramolecular Catalyst (Angew. Chem. Int. Ed. 18/2018) Angewandte Chemie International Edition. 57: 4805-4805. DOI: 10.1002/Anie.201802931 |
0.347 |
|
| 2018 |
Wenz KM, Leonhardt-Lutterbeck G, Breit B. Titelbild: Inducing Axial Chirality in a Supramolecular Catalyst (Angew. Chem. 18/2018) Angewandte Chemie. 130: 4897-4897. DOI: 10.1002/Ange.201802931 |
0.35 |
|
| 2017 |
Breit B, Zhou Y. Rhodium Catalyzed Asymmetric N-H Functionalization of Quinazolinones with Allenes and Allylic Carbonates: The First Enantioselective Formal Total Synthesis of (-)-Chaetominine. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29105185 DOI: 10.1002/Chem.201705059 |
0.45 |
|
| 2017 |
Breit B, Haydl A, Lang T, Krische M. Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition Metal Catalysis. Angewandte Chemie (International Ed. in English). PMID 28605083 DOI: 10.1002/Anie.201704248 |
0.78 |
|
| 2017 |
Breit B, Kuang J, Parveen S. Rhodium-Catalyzed Regioselective Domino Azlactone-Alkyne Coupling/Aza-Cope Rearrangement: A Facile Access to 2-Allyl-3-oxazolin-5-ones and Trisubstituted Pyridines. Angewandte Chemie (International Ed. in English). PMID 28514115 DOI: 10.1002/Anie.201704022 |
0.458 |
|
| 2017 |
Parveen S, Li C, Hassan A, Breit B. Chemo-, Regio-, and Enantioselective Rhodium-Catalyzed Allylation of Pyridazinones with Terminal Allenes. Organic Letters. PMID 28422507 DOI: 10.1021/Acs.Orglett.7B00718 |
0.432 |
|
| 2017 |
Khakyzadeh V, Wang YH, Breit B. Rhodium-catalyzed addition of sulfonyl hydrazides to allenes: regioselective synthesis of branched allylic sulfones. Chemical Communications (Cambridge, England). PMID 28422264 DOI: 10.1039/C7Cc02375H |
0.487 |
|
| 2017 |
Breit B, Schmidt J, Li C. Transition Metal Catalyzed Regiodivergent and Stereoselective Access to Branched and Linear Allylated 4 Pyridones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28370612 DOI: 10.1002/Chem.201701382 |
0.438 |
|
| 2017 |
Thieme N, Breit B. Enantioselective and Regiodivergent Addition of Purines to Terminal Allenes: Synthesis of Abacavir. Angewandte Chemie (International Ed. in English). PMID 28079946 DOI: 10.1002/Anie.201610876 |
0.462 |
|
| 2017 |
Beck TM, Breit B. Regio- and Enantioselective Rhodium-Catalyzed Addition of 1,3-Diketones to Allenes: Construction of Asymmetric Tertiary and Quaternary All Carbon Centers. Angewandte Chemie (International Ed. in English). PMID 28075513 DOI: 10.1002/Anie.201610577 |
0.473 |
|
| 2017 |
Carreira EM, Wolleb H, Haydl AM, Breit B. Synthesis of Epothilone D Synfacts. 13: 121-121. DOI: 10.1055/S-0036-1589872 |
0.751 |
|
| 2017 |
Ullrich J, Breit B. Selective Hydrogenation of Carboxylic Acids to Alcohols or Alkanes Employing a Heterogeneous Catalyst Acs Catalysis. 8: 785-789. DOI: 10.1021/Acscatal.7B03484 |
0.355 |
|
| 2017 |
Haydl AM, Breit B, Liang T, Krische MJ. Alkine als alternativer Einstieg in elektrophile und nukleophile Übergangsmetall-katalysierte Allylierungen Angewandte Chemie. 129: 11466-11480. DOI: 10.1002/Ange.201704248 |
0.736 |
|
| 2016 |
Xu K, Wang YH, Khakyzadeh V, Breit B. Asymmetric synthesis of allylic amines hydroamination of allenes with benzophenone imine. Chemical Science. 7: 3313-3316. PMID 29997823 DOI: 10.1039/C5Sc04984A |
0.58 |
|
| 2016 |
Spreider PA, Haydl AM, Heinrich M, Breit B. Rhodium-Catalyzed Diastereoselective Cyclization of Allenyl-Sulfonylcarbamates: A Stereodivergent Approach to 1,3-Aminoalcohol Derivatives. Angewandte Chemie (International Ed. in English). PMID 27862829 DOI: 10.1002/Anie.201609366 |
0.802 |
|
| 2016 |
Breit B, Haydl A. All for One and One for All: The Total Synthesis of Epothilone D. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27792853 DOI: 10.1002/Chem.201605011 |
0.797 |
|
| 2016 |
Li C, Breit B. Rhodium-Catalyzed Dynamic Kinetic Asymmetric Allylation of Phenols and 2-Hydroxypyridines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27620970 DOI: 10.1002/Chem.201603532 |
0.435 |
|
| 2016 |
Koschker P, Breit B. Branching Out: Rhodium-Catalyzed Allylation with Alkynes and Allenes. Accounts of Chemical Research. PMID 27455048 DOI: 10.1021/Acs.Accounts.6B00252 |
0.514 |
|
| 2016 |
Ganss S, Breit B. Enantioselective Rhodium-Catalyzed Atom-Economical Macrolactonization. Angewandte Chemie (International Ed. in English). PMID 27383766 DOI: 10.1002/Anie.201604301 |
0.473 |
|
| 2016 |
Liu Z, Breit B. Rhodium-Catalyzed Enantioselective Intermolecular Hydroalkoxylation of Allenes and Alkynes with Alcohols: Synthesis of Branched Allylic Ethers. Angewandte Chemie (International Ed. in English). PMID 27244349 DOI: 10.1002/Anie.201603538 |
0.438 |
|
| 2016 |
Haydl AM, Berthold D, Spreider PA, Breit B. Stereodivergent and Protecting-Group-Free Synthesis of the Helicascolide Family: A Rhodium-Catalyzed Atom-Economical Lactonization Strategy. Angewandte Chemie (International Ed. in English). PMID 27043137 DOI: 10.1002/Anie.201600632 |
0.794 |
|
| 2016 |
Li C, Grugel CP, Breit B. Rhodium-catalyzed chemo- and regioselective decarboxylative addition of β-ketoacids to alkynes. Chemical Communications (Cambridge, England). PMID 27040888 DOI: 10.1039/C6Cc02272C |
0.444 |
|
| 2016 |
Breit B, Haydl A, Hilpert L. Regioconvergent and Enantioselective Rhodium-Catalyzed Hydroamination of Internal and Terminal Alkynes: A Highly Flexible Access to Chiral Pyrazoles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26990445 DOI: 10.1002/Chem.201601198 |
0.812 |
|
| 2016 |
Lautens M, Johnson T, Ganss S, Breit B. Rhodium-Catalyzed Enantioselective Macrolactonization Synfacts. 12: 929-929. DOI: 10.1055/S-0035-1561901 |
0.563 |
|
| 2016 |
Beck TM, Breit B. Regioselective Rhodium-Catalyzed Addition of β-Keto Esters, β-Keto Amides, and 1,3-Diketones to Internal Alkynes European Journal of Organic Chemistry. 2016: 5839-5844. DOI: 10.1002/Ejoc.201601230 |
0.417 |
|
| 2016 |
Ganss S, Pedroni J, Lumbroso A, Leonhardt‐Lutterbeck G, Meißner A, Wei S, Drexler H, Heller D, Breit B. Rhodium-Catalyzed Addition of Carboxylic Acids to Terminal Alkynes towards Z-Enol Esters Organic Syntheses. 93: 367-384. DOI: 10.1002/0471264229.Os093.27 |
0.379 |
|
| 2015 |
Beck TM, Breit B. Regioselective Rhodium-Catalyzed Addition of 1,3-Dicarbonyl Compounds to Terminal Alkynes. Organic Letters. PMID 26683497 DOI: 10.1021/Acs.Orglett.5B03391 |
0.473 |
|
| 2015 |
Haydl AM, Breit B. Atom-Economical Dimerization Strategy by the Rhodium-Catalyzed Addition of Carboxylic Acids to Allenes: Protecting-Group-Free Synthesis of Clavosolide A and Late-Stage Modification. Angewandte Chemie (International Ed. in English). PMID 26553131 DOI: 10.1002/Anie.201506618 |
0.787 |
|
| 2015 |
Pritzius AB, Breit B. Z-Selective Hydrothiolation of Racemic 1,3-Disubstituted Allenes: An Atom-Economic Rhodium-Catalyzed Dynamic Kinetic Resolution. Angewandte Chemie (International Ed. in English). PMID 26418035 DOI: 10.1002/Anie.201507623 |
0.444 |
|
| 2015 |
Xu K, Gilles T, Breit B. Asymmetric synthesis of N-allylic indoles via regio- and enantioselective allylation of aryl hydrazines. Nature Communications. 6: 7616. PMID 26137886 DOI: 10.1038/Ncomms8616 |
0.543 |
|
| 2015 |
Xu K, Raimondi W, Bury T, Breit B. Enantioselective formation of tertiary and quaternary allylic C-N bonds via allylation of tetrazoles. Chemical Communications (Cambridge, England). 51: 10861-3. PMID 26051122 DOI: 10.1039/C5Cc04203H |
0.538 |
|
| 2015 |
Haydl AM, Xu K, Breit B. Regio- and enantioselective synthesis of N-substituted pyrazoles by rhodium-catalyzed asymmetric addition to allenes. Angewandte Chemie (International Ed. in English). 54: 7149-53. PMID 25926026 DOI: 10.1002/Anie.201501758 |
0.823 |
|
| 2015 |
Köpfer A, Breit B. Rhodium-Catalyzed Hydroformylation of 1,1-Disubstituted Allenes Employing the Self-Assembling 6-DPPon System. Angewandte Chemie (International Ed. in English). 54: 6913-7. PMID 25917327 DOI: 10.1002/Anie.201502086 |
0.432 |
|
| 2015 |
Koschker P, Kähny M, Breit B. Enantioselective redox-neutral Rh-catalyzed coupling of terminal alkynes with carboxylic acids toward branched allylic esters. Journal of the American Chemical Society. 137: 3131-7. PMID 25667963 DOI: 10.1021/Jacs.5B01131 |
0.467 |
|
| 2015 |
Pritzius AB, Breit B. Asymmetric rhodium-catalyzed addition of thiols to allenes: synthesis of branched allylic thioethers and sulfones. Angewandte Chemie (International Ed. in English). 54: 3121-5. PMID 25598017 DOI: 10.1002/Anie.201411402 |
0.486 |
|
| 2015 |
Wünsch S, Breit B. Probing o-diphenylphosphanyl benzoate (o-DPPB)-directed C-C bond formation: total synthesis of dictyostatin. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 2358-63. PMID 25524890 DOI: 10.1002/Chem.201406252 |
0.38 |
|
| 2015 |
Sam B, Breit B, Krische MJ. Paraformaldehyde and methanol as C1 feedstocks in metal-catalyzed C-C couplings of π-unsaturated reactants: beyond hydroformylation. Angewandte Chemie (International Ed. in English). 54: 3267-74. PMID 25430585 DOI: 10.1002/Anie.201407888 |
0.569 |
|
| 2015 |
Allmendinger S, Kinuta H, Breit B. Asymmetric Hydroformylation of Vinylarenes via Rhodium Catalysis Synfacts. 11: 401-401. DOI: 10.1055/S-0034-1380477 |
0.455 |
|
| 2015 |
Xu K, Raimondi W, Bury T, Breit B. Enantioselective formation of tertiary and quaternary allylic C-N bonds via allylation of tetrazoles Chemical Communications. 51: 10861-10863. DOI: 10.1039/c5cc04203h |
0.395 |
|
| 2015 |
Gellrich U, Koslowski T, Breit B. Full kinetic analysis of a rhodium-catalyzed hydroformylation: Beyond the rate-limiting step picture Catalysis Science and Technology. 5: 129-133. DOI: 10.1039/C4Cy01209G |
0.342 |
|
| 2015 |
Xu K, Gilles T, Breit B. Asymmetric synthesis of N-allylic indoles via regio- and enantioselective allylation of aryl hydrazines Nature Communications. 6. DOI: 10.1038/ncomms8616 |
0.5 |
|
| 2015 |
Koschker P, Kähny M, Breit B. Enantioselective redox-neutral Rh-catalyzed coupling of terminal alkynes with carboxylic acids toward branched allylic esters Journal of the American Chemical Society. 137: 3131-3137. DOI: 10.1021/jacs.5b01131 |
0.303 |
|
| 2015 |
Li C, Kaehny M, Breit B. ChemInform Abstract: Rhodium-Catalyzed Chemo-, Regio-, and Enantioselective Addition of 2-Pyridones to Terminal Allenes. Cheminform. 46: no-no. DOI: 10.1002/chin.201519196 |
0.348 |
|
| 2015 |
Haydl AM, Xu K, Breit B. Regio- and Enantioselective Synthesis of N-Substituted Pyrazoles by Rhodium-Catalyzed Asymmetric Addition to Allenes Angewandte Chemie - International Edition. 54: 7149-7153. DOI: 10.1002/anie.201501758 |
0.808 |
|
| 2015 |
Pritzius AB, Breit B. Asymmetric rhodium-catalyzed addition of thiols to allenes: Synthesis of branched allylic thioethers and sulfones Angewandte Chemie - International Edition. 54: 3121-3125. DOI: 10.1002/anie.201411402 |
0.394 |
|
| 2014 |
Xu K, Khakyzadeh V, Bury T, Breit B. Direct transformation of terminal alkynes to branched allylic sulfones. Journal of the American Chemical Society. 136: 16124-7. PMID 25365339 DOI: 10.1021/Ja509383R |
0.528 |
|
| 2014 |
Li C, Kähny M, Breit B. Rhodium-catalyzed chemo-, regio-, and enantioselective addition of 2-pyridones to terminal allenes Angewandte Chemie - International Edition. 53: 13780-13784. PMID 25298286 DOI: 10.1002/Anie.201407935 |
0.441 |
|
| 2014 |
Fanfoni L, Diab L, Smejkal T, Breit B. Efficient synthesis of new fluorinated building blocks by means of hydroformylation. Chimia. 68: 371-7. PMID 25198747 DOI: 10.2533/Chimia.2014.371 |
0.447 |
|
| 2014 |
Xu K, Thieme N, Breit B. Unlocking the N(2) selectivity of benzotriazoles: regiodivergent and highly selective coupling of benzotriazoles with allenes. Angewandte Chemie (International Ed. in English). 53: 7268-71. PMID 24863853 DOI: 10.1002/Anie.201403682 |
0.47 |
|
| 2014 |
Breit B, Gellrich U, Li T, Lynam JM, Milner LM, Pridmore NE, Slattery JM, Whitwood AC. Mechanistic insight into the ruthenium-catalysed anti-Markovnikov hydration of alkynes using a self-assembled complex: a crucial role for ligand-assisted proton shuttle processes. Dalton Transactions (Cambridge, England : 2003). 43: 11277-85. PMID 24828970 DOI: 10.1039/C4Dt00712C |
0.34 |
|
| 2014 |
Schotes C, Ostrovskyi D, Senger J, Schmidtkunz K, Jung M, Breit B. Total synthesis of (18S)- and (18R)-homolargazole by rhodium-catalyzed hydrocarboxylation Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 2164-2168. PMID 24478039 DOI: 10.1002/Chem.201303300 |
0.417 |
|
| 2014 |
Xu K, Thieme N, Breit B. Atom-economic, regiodivergent, and stereoselective coupling of imidazole derivatives with terminal allenes Angewandte Chemie - International Edition. 53: 2162-2165. PMID 24446318 DOI: 10.1002/Anie.201309126 |
0.515 |
|
| 2014 |
Li C, Breit B. Rhodium-catalyzed chemo- and regioselective decarboxylative addition of β-ketoacids to allenes: efficient construction of tertiary and quaternary carbon centers. Journal of the American Chemical Society. 136: 862-5. PMID 24397382 DOI: 10.1021/Ja411397G |
0.348 |
|
| 2014 |
Gellrich U, Meißner A, Steffani A, Kähny M, Drexler HJ, Heller D, Plattner DA, Breit B. Mechanistic investigations of the rhodium catalyzed propargylic CH activation. Journal of the American Chemical Society. 136: 1097-104. PMID 24377792 DOI: 10.1021/Ja411204D |
0.361 |
|
| 2014 |
Lautens M, Le CM, Xu K, Thieme N, Breit B. Regiodivergent and Stereoselective Coupling of Imidazoles with Allenes Synfacts. 10: 379-379. DOI: 10.1055/S-0033-1341016 |
0.422 |
|
| 2014 |
Diezel S, Breit B. Tandem regioselective rhodium-catalyzed hydroformylation-enantioselective aminocatalytic anti -Mannich reaction Synthesis (Germany). 46: 1311-1320. DOI: 10.1055/S-0033-1338602 |
0.434 |
|
| 2014 |
Xu K, Khakyzadeh V, Bury T, Breit B. Direct transformation of terminal alkynes to branched allylic sulfones Journal of the American Chemical Society. 136: 16124-16127. DOI: 10.1021/ja509383r |
0.354 |
|
| 2014 |
Ruan Q, Zhou L, Breit B. New phosphorus self-assembling ligands for the tandem hydroformylation- Wittig olefination reaction of homoallylic alcohols - A key step for stereoselective pyran synthesis Catalysis Communications. 53: 87-90. DOI: 10.1016/J.Catcom.2014.04.022 |
0.429 |
|
| 2014 |
Xu K, Thieme N, Breit B. Unlocking the N2selectivity of benzotriazoles: Regiodivergent and highly selective coupling of benzotriazoles with allenes Angewandte Chemie - International Edition. 53: 7268-7271. DOI: 10.1002/anie.201403682 |
0.351 |
|
| 2014 |
Sam B, Breit B, Krische MJ. Paraformaldehyd und Methanol als C1-Rohstoffe in metallkatalysierten C-C-Kupplungen π-ungesättigter Edukte Angewandte Chemie. 127: 3317-3325. DOI: 10.1002/Ange.201407888 |
0.455 |
|
| 2014 |
Allmendinger S, Kinuta H, Breit B. Easily accessible TADDOL-derived bisphosphonite ligands: Synthesis and application in the asymmetric hydroformylation of vinylarenes Advanced Synthesis and Catalysis. 357: 41-45. DOI: 10.1002/Adsc.201400657 |
0.449 |
|
| 2013 |
Gellrich U, Himmel D, Meuwly M, Breit B. Realistic energy surfaces for real-world systems: an IMOMO CCSD(T):DFT scheme for rhodium-catalyzed hydroformylation with the 6-DPPon ligand. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 16272-81. PMID 24127405 DOI: 10.1002/Chem.201302132 |
0.329 |
|
| 2013 |
Diab L, Gellrich U, Breit B. Tandem decarboxylative hydroformylation-hydrogenation reaction of α,β-unsaturated carboxylic acids toward aliphatic alcohols under mild conditions employing a supramolecular catalyst system. Chemical Communications (Cambridge, England). 49: 9737-9. PMID 24022335 DOI: 10.1039/C3Cc45547E |
0.405 |
|
| 2013 |
Wei S, Pedroni J, Meißner A, Lumbroso A, Drexler HJ, Heller D, Breit B. Development of an improved rhodium catalyst for z-selective anti-markovnikov addition of carboxylic acids to terminal alkynes. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 12067-76. PMID 23873816 DOI: 10.1002/Chem.201300160 |
0.392 |
|
| 2013 |
Lumbroso A, Cooke ML, Breit B. Catalytic asymmetric synthesis of allylic alcohols and derivatives and their applications in organic synthesis. Angewandte Chemie (International Ed. in English). 52: 1890-932. PMID 23319206 DOI: 10.1002/Anie.201204579 |
0.415 |
|
| 2013 |
Stein M, Breit B. Catalytic hydrogenation of amides to amines under mild conditions. Angewandte Chemie (International Ed. in English). 52: 2231-4. PMID 23225730 DOI: 10.1002/Anie.201207803 |
0.324 |
|
| 2013 |
Aureggi V, Ehmke V, Wieland J, Schweizer WB, Bernet B, Bur D, Meyer S, Rottmann M, Freymond C, Brun R, Breit B, Diederich F. Potent inhibitors of malarial aspartic proteases, the plasmepsins, by hydroformylation of substituted 7-azanorbornenes Chemistry - a European Journal. 19: 155-164. PMID 23161835 DOI: 10.1002/Chem.201202941 |
0.329 |
|
| 2013 |
Lautens M, Zhang L, Agabekov V, Seiche W, Breit B. Self-Assembling Ligand/Rhodium-Catalyzed Alkyne Hydroformylation Synfacts. 9: 865-865. DOI: 10.1055/S-0033-1339389 |
0.414 |
|
| 2013 |
Fuchs D, Nasr-Esfahani M, Diab L, Šmejkal T, Breit B. Tandem hydroformylation-biginelli reaction Synlett. 24: 1657-1662. DOI: 10.1055/S-0033-1339298 |
0.398 |
|
| 2013 |
Agabekov V, Seiche W, Breit B. Rhodium-catalyzed hydroformylation of alkynes employing a self-assembling ligand system Chemical Science. 4: 2418-2422. DOI: 10.1039/C3Sc50725D |
0.391 |
|
| 2013 |
Köpfer A, Sam B, Breit B, Krische MJ. Regiodivergent reductive coupling of 2-substituted dienes to formaldehyde employing ruthenium or nickel catalyst: Hydrohydroxymethylation via transfer hydrogenation Chemical Science. 4: 1876-1880. DOI: 10.1039/C3Sc22051F |
0.526 |
|
| 2013 |
Breit B. Fascination of organic synthesis | Faszination Organische Synthese Chemie in Unserer Zeit. 47: 139. DOI: 10.1002/Ciuz.201380002 |
0.342 |
|
| 2013 |
Lumbroso A, Cooke ML, Breit B. Katalytische asymmetrische Synthese von Allylalkoholen und Allylalkohol-Derivaten und deren Anwendung in der organischen Synthese Angewandte Chemie. 125: 1942-1986. DOI: 10.1002/Ange.201204579 |
0.341 |
|
| 2012 |
Huang J, Häussinger D, Gellrich U, Seiche W, Breit B, Meuwly M. Hydrogen-bond and solvent dynamics in transition metal complexes: A combined simulation and NMR-investigation Journal of Physical Chemistry B. 116: 14406-14415. PMID 23127212 DOI: 10.1021/Jp309412R |
0.301 |
|
| 2012 |
Gellrich U, Seiche W, Keller M, Breit B. Mechanistic insights into a supramolecular self-assembling catalyst system: Evidence for hydrogen bonding during rhodium-catalyzed hydroformylation Angewandte Chemie - International Edition. 51: 11033-11038. PMID 23023718 DOI: 10.1002/Anie.201203768 |
0.33 |
|
| 2012 |
Cooke ML, Xu K, Breit B. Enantioselective rhodium-catalyzed synthesis of branched allylic amines by intermolecular hydroamination of terminal allenes. Angewandte Chemie (International Ed. in English). 51: 10876-9. PMID 23011801 DOI: 10.1002/Anie.201206594 |
0.584 |
|
| 2012 |
Schmidt Y, Lehr K, Colas L, Breit B. Assignment of relative configuration of desoxypropionates by 1hnmr spectroscopy: Method development, proof of principle by asymmetric total synthesis of xylarinic acid a and applications Chemistry - a European Journal. 18: 7071-7081. PMID 22544461 DOI: 10.1002/Chem.201103988 |
0.353 |
|
| 2012 |
Reichle MA, Breit B. Preparation of alkylmagnesium reagents from alkenes through hydroboration and boron-magnesium exchange Angewandte Chemie - International Edition. 51: 5730-5734. PMID 22528344 DOI: 10.1002/Anie.201201704 |
0.361 |
|
| 2012 |
Fuchs D, Rousseau G, Diab L, Gellrich U, Breit B. Tandem rhodium-catalyzed hydroformylation-hydrogenation of alkenes by employing a cooperative ligand system. Angewandte Chemie (International Ed. in English). 51: 2178-82. PMID 22290636 DOI: 10.1002/Anie.201108946 |
0.361 |
|
| 2012 |
Lumbroso A, Abermil N, Breit B. Atom economic macrolactonization and lactonization via redox-neutral rhodium-catalyzed coupling of terminal alkynes with carboxylic acids Chemical Science. 3: 789-793. DOI: 10.1039/C2Sc00812B |
0.368 |
|
| 2012 |
Cooke ML, Xu K, Breit B. Enantioselective rhodium-catalyzed synthesis of branched allylic amines by intermolecular hydroamination of terminal allenes Angewandte Chemie - International Edition. 51: 10876-10879. DOI: 10.1002/anie.201206594 |
0.522 |
|
| 2011 |
Koschker P, Lumbroso A, Breit B. Enantioselective synthesis of branched allylic esters via rhodium-catalyzed coupling of allenes with carboxylic acids. Journal of the American Chemical Society. 133: 20746-9. PMID 22111875 DOI: 10.1021/Ja210149G |
0.432 |
|
| 2011 |
Schmidt Y, Breit B. Stereoselective and diversity-oriented synthesis of trisubstituted allylic alcohols and amines Chemistry - a European Journal. 17: 11789-11796. PMID 21898610 DOI: 10.1002/Chem.201100844 |
0.416 |
|
| 2011 |
Schmidt Y, Breit B. Stereoselective synthesis of trisubstituted olefins by a directed allylic substitution strategy Chemistry - a European Journal. 17: 11780-11788. PMID 21887831 DOI: 10.1002/Chem.201100843 |
0.448 |
|
| 2011 |
Ueki Y, Ito H, Usui I, Breit B. Formation of quaternary carbon centers by highly regioselective hydroformylation with catalytic amounts of a reversibly bound directing group. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 8555-8. PMID 21728199 DOI: 10.1002/Chem.201101186 |
0.33 |
|
| 2011 |
Vautravers NR, Regent DD, Breit B. Inter- and intramolecular hydroacylation of alkenes employing a bifunctional catalyst system. Chemical Communications (Cambridge, England). 47: 6635-7. PMID 21566809 DOI: 10.1039/C1Cc10683J |
0.421 |
|
| 2011 |
Bausch CC, Patman RL, Breit B, Krische MJ. Divergent regioselectivity in the synthesis of trisubstituted allylic alcohols by nickel- and ruthenium-catalyzed alkyne hydrohydroxymethylation with formaldehyde. Angewandte Chemie (International Ed. in English). 50: 5687-90. PMID 21557426 DOI: 10.1002/Anie.201101496 |
0.555 |
|
| 2011 |
Rousseau G, Breit B. Removable directing groups in organic synthesis and catalysis. Angewandte Chemie (International Ed. in English). 50: 2450-94. PMID 21365719 DOI: 10.1002/Anie.201006139 |
0.377 |
|
| 2011 |
Lumbroso A, Koschker P, Vautravers NR, Breit B. Redox-neutral atom-economic rhodium-catalyzed coupling of terminal alkynes with carboxylic acids toward branched allylic esters Journal of the American Chemical Society. 133: 2386-2389. PMID 21291216 DOI: 10.1021/Ja1108613 |
0.422 |
|
| 2011 |
Usui I, Nomura K, Breit B. Diastereoselective hydroformylation of 2,5-cyclohexadienyl-1-carbinols with catalytic amounts of a reversibly bound directing group. Organic Letters. 13: 612-5. PMID 21229981 DOI: 10.1021/Ol1028546 |
0.319 |
|
| 2011 |
Gellrich U, Huang J, Seiche W, Keller M, Meuwly M, Breit B. Ligand self-assembling through complementary hydrogen-bonding in the coordination sphere of a transition metal center: the 6-diphenylphosphanylpyridin-2(1H)-one system. Journal of the American Chemical Society. 133: 964-75. PMID 21142007 DOI: 10.1021/Ja108639E |
0.307 |
|
| 2011 |
Vautravers NR, Breit B. Rhodium(I)-catalyzed 1,4-addition of arylboronic acids to acrylic acid in water: One-step preparation of 3-arylpropionic acids Synlett. 2517-2520. DOI: 10.1055/S-0030-1260319 |
0.331 |
|
| 2011 |
Lumbroso A, Koschker P, Vautravers NR, Breit B. Rhodium-Catalyzed Coupling of Terminal Alkynes with CarboxylicAcids Synfacts. 2011: 536-536. DOI: 10.1055/S-0030-1259784 |
0.364 |
|
| 2011 |
Koschker P, Lumbroso A, Breit B. Enantioselective synthesis of branched allylic esters via rhodium-catalyzed coupling of allenes with carboxylic acids Journal of the American Chemical Society. 133: 20746-20749. DOI: 10.1021/ja210149g |
0.338 |
|
| 2011 |
Rousseau G, Breit B. Corrigendum: Removable Directing Groups in Organic Synthesis and Catalysis Angewandte Chemie International Edition. 50: 5007-5007. DOI: 10.1002/Anie.201101929 |
0.325 |
|
| 2011 |
Rousseau G, Breit B. Berichtigung: Entfernbare dirigierende Gruppen in der organischen Synthese und Katalyse Angewandte Chemie. 123: 5111-5111. DOI: 10.1002/Ange.201101929 |
0.347 |
|
| 2010 |
Lumbroso A, Vautravers NR, Breit B. Rhodium-catalyzed selective anti-Markovnikov addition of carboxylic acids to alkynes. Organic Letters. 12: 5498-501. PMID 21049947 DOI: 10.1021/Ol102365E |
0.419 |
|
| 2010 |
Wieland J, Breit B. A combinatorial approach to the identification of self-assembled ligands for rhodium-catalysed asymmetric hydrogenation Nature Chemistry. 2: 832-837. PMID 20861898 DOI: 10.1038/Nchem.800 |
0.355 |
|
| 2010 |
Schmidt Y, Lehr K, Breuninger U, Brand G, Reiss T, Breit B. Enantioselective total synthesis of the unnatural and the natural stereoisomers of vittatalactone Journal of Organic Chemistry. 75: 4424-4433. PMID 20527973 DOI: 10.1021/Jo100383U |
0.404 |
|
| 2010 |
Laemmerhold KM, Breit B. Total synthesis of (+)-clavolonine, (-)-deacetylfawcettiine, and (+)-acetylfawcettiine Angewandte Chemie - International Edition. 49: 2367-2370. PMID 20209551 DOI: 10.1002/Anie.200907248 |
0.381 |
|
| 2010 |
Kemme ST, Smejkal T, Breit B. Combined transition-metal- and organocatalysis: an atom economic C3 homologation of alkenes to carbonyl and carboxylic compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 3423-33. PMID 20131344 DOI: 10.1002/Chem.200903223 |
0.347 |
|
| 2010 |
Šmejkal T, Gribkov D, Geier J, Keller M, Breit B. Transition-state stabilization by a secondary substrate-ligand interaction: A new design principle for highly efficient transition-metal catalysis Chemistry - a European Journal. 16: 2470-2478. PMID 20077538 DOI: 10.1002/Chem.200902553 |
0.392 |
|
| 2010 |
Airiau E, Spangenberg T, Girard N, Breit B, Mann A. Short access to (+)-lupinine and (+)-epiquinamide via double hydroformylation Organic Letters. 12: 528-531. PMID 20038131 DOI: 10.1021/Ol902718Q |
0.376 |
|
| 2010 |
Kemme ST, Schmidt Y, Grünanger CU, Laungani AC, Herber C, Breit B. Economic large-scale synthesis of o - And m -diphenylphosphinobenzoic acids Synthesis. 1924-1928. DOI: 10.1055/S-0029-1218705 |
0.305 |
|
| 2010 |
Beierlein CH, Breit B, Paz Schmidt RA, Plattner DA. Online monitoring of hydroformylation intermediates by ESI-MS Organometallics. 29: 2521-2532. DOI: 10.1021/Om100131T |
0.344 |
|
| 2010 |
Spangenberg T, Schoenfelder A, Breit B, Mann A. 1,2-diastereoselective C-C bond-forming reactions for the synthesis of chiral β-branched α-amino acids European Journal of Organic Chemistry. 6005-6018. DOI: 10.1002/Ejoc.201000865 |
0.407 |
|
| 2010 |
REGITZ M, WEITLING T, FAESSLER R, BREIT B, GEISSLER B, JULINO M, HOFFMANN A, BERGSTRAESSER U. ChemInform Abstract: Organophosphorus Compounds. Part 108. Directed Synthesis of Phosphorus- Carbon Cage Compounds - A Challenge in Organophosphorus Chemistry Cheminform. 28: no-no. DOI: 10.1002/chin.199711290 |
0.404 |
|
| 2010 |
TROST BM, BREIT B, PEUKERT S, ZAMBRANO J, ZILLER JW. ChemInform Abstract: A New Platform for Designing Ligands for Asymmetric Induction in Allylic Alkylations. Cheminform. 27: no-no. DOI: 10.1002/chin.199608033 |
0.688 |
|
| 2010 |
REGITZ M, BREIT B, MEMMESHEIMER H. ChemInform Abstract: The Cyclotetramerization of Phosphaalkynes and Its 31P NMR Spectroscopic Consequences Cheminform. 26: no-no. DOI: 10.1002/chin.199542312 |
0.321 |
|
| 2010 |
BREIT B, HOFFMANN A, BERGSTRAESSER U, RICARD L, MATHEY F, REGITZ M. ChemInform Abstract: Phosphorus Compounds. Part 77. The First Carbon-Phosphorus-Aluminum Cage Compounds: Cyclooligomerization of Phosphaalkynes with Trialkylaluminum Compounds. Cheminform. 25: no-no. DOI: 10.1002/chin.199450191 |
0.349 |
|
| 2010 |
BREIT B, REGITZ M. ChemInform Abstract: Organophosphorus Compounds. Part 71. Phosphaalkynes and Phosphaalkenes as Trapping Partners for 1,2-Dehydrobenzene and Phenylium-2- carboxylate. Cheminform. 25: no-no. DOI: 10.1002/chin.199424091 |
0.369 |
|
| 2010 |
BREIT B, BOESE R, REGITZ M. ChemInform Abstract: Organo-Phosphorus Compounds. Part 73. Trapping Reaction of an in situ Generated Silene with tBu-CP. Formation of a Diphosphatricyclobenzoheptane. Cheminform. 25: no-no. DOI: 10.1002/chin.199416217 |
0.424 |
|
| 2010 |
BREIT B, REGITZ M. ChemInform Abstract: Organophosphorus Compounds. Part 65. The Phospha-Ane Reaction: An Unusual Dimerization of Phosphaalkenes. Cheminform. 24: no-no. DOI: 10.1002/chin.199339247 |
0.422 |
|
| 2010 |
REGITZ M, WETTLING T, BREIT B, BIRKEL M, GEISSLER B, BERGSTRAESSER U, BARTH S, BINGER P. ChemInform Abstract: Organophosphorus Compounds. Part 62. The Mediated Cyclooligomerization of Phosphaalkynes - New Aspects in the Synthesis of Polycyclic Phosphorus Compounds Cheminform. 24: no-no. DOI: 10.1002/chin.199335250 |
0.406 |
|
| 2010 |
BREIT B, BERGSTRAESSER U, MAAS G, REGITZ M. ChemInform Abstract: Phosphorus Compounds. Part 58. Spirocyclization of a Stable Phosphaalkyne with Aluminum Trichloride: Key Reaction for the Production of Triphospha Dewar Benzene Derivatives. Cheminform. 23: no-no. DOI: 10.1002/chin.199246215 |
0.455 |
|
| 2010 |
FUCHS E, BREIT B, BERGSTRAESSER U, HOFFMANN J, HEYDT H, REGITZ M. ChemInform Abstract: Organophosphorus Compounds. Part 52. Phosphatriafulvenes and Their Reaction with Electrophiles. Cheminform. 23: no-no. DOI: 10.1002/chin.199226217 |
0.427 |
|
| 2010 |
BREIT B, MEMMESHEIMER H, BOESE R, REGITZ M. ChemInform Abstract: Organophosphorus Compounds. Part 53. Cyclopropenylidene-methylene- diphosphanes - New Cross-Conjugated Phosphapolyenes. Cheminform. 23: no-no. DOI: 10.1002/chin.199222214 |
0.376 |
|
| 2010 |
FUCHS E, BREIT B, HEYDT H, SCHOELLER W, BUSCH T, KRUEGER C, BETZ P, REGITZ M. ChemInform Abstract: Organophosphorus Compounds. Part 51. Phosphatriafulvenes - Phosphaalkenes with Inverse Electron Density. Cheminform. 23: no-no. DOI: 10.1002/chin.199208255 |
0.326 |
|
| 2009 |
Schmidt Y, Breit B. Enantioselective total synthesis and determination of absolute configuration of vittatalactone Organic Letters. 11: 4767-4769. PMID 19791774 DOI: 10.1021/Ol901591T |
0.44 |
|
| 2009 |
Brand GJ, Studte C, Breit B. Iterative synthesis of (oligo)deoxypropionates via zinc-catalyzed enantiospecific sp3-sp3 cross-coupling. Organic Letters. 11: 4668-70. PMID 19761193 DOI: 10.1021/Ol901944B |
0.401 |
|
| 2009 |
Reiss T, Breit B. Total synthesis of (+)-bourgeanic acid utilizing o-DPPB-directed allylic substitution Organic Letters. 11: 3286-3289. PMID 19719180 DOI: 10.1021/Ol9011635 |
0.415 |
|
| 2009 |
Smejkal T, Han H, Breit B, Krische MJ. All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation. Journal of the American Chemical Society. 131: 10366-7. PMID 19594163 DOI: 10.1021/Ja904124B |
0.566 |
|
| 2009 |
Reiss T, Breit B. A unified strategy for the stereospecific construction of propionates and acetate-propionates relying on a directed allylic substitution. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 6345-8. PMID 19479928 DOI: 10.1002/Chem.200901064 |
0.321 |
|
| 2009 |
Usui I, Schmidt S, Breit B. Dual palladium- and proline-catalyzed allylic alkylation of enolizable ketones and aldehydes with allylic alcohols. Organic Letters. 11: 1453-6. PMID 19243116 DOI: 10.1021/Ol9001812 |
0.383 |
|
| 2009 |
Bigot A, Breuninger D, Breit B. Desymmetrizing Hydroformylation/Carbonyl Ene Cyclization Synfacts. 2009: 423-423. DOI: 10.1055/S-0028-1087874 |
0.431 |
|
| 2009 |
Breit B. ChemInform Abstract: Aliphatic and Alicyclic Aldehydes: Synthesis by Hydroformylation of Alkenes Cheminform. 40. DOI: 10.1002/chin.200902238 |
0.354 |
|
| 2008 |
Breit B, Bigot A. Enantioselective synthesis of 2,6-dideoxy carbasugars based on a desymmetrizing hydroformylation-carbonyl ene cyclization process Chemical Communications. 6498-6500. PMID 19057758 DOI: 10.1039/B817786D |
0.439 |
|
| 2008 |
Bigot A, Breuninger D, Breit B. One-pot desymmetrizing hydroformylation/carbonyl ene cyclization process: Straightforward access to highly functionalized cyclohexanols Organic Letters. 10: 5321-5324. PMID 19006319 DOI: 10.1021/Ol8016148 |
0.431 |
|
| 2008 |
Breit B, Schmidt Y. Directed reactions of organocopper reagents Chemical Reviews. 108: 2928-2951. PMID 18698734 DOI: 10.1021/Cr078352C |
0.337 |
|
| 2008 |
Grünanger CU, Breit B. Branched-regioselective hydroformylation with catalytic amounts of a reversibly bound directing group. Angewandte Chemie (International Ed. in English). 47: 7346-9. PMID 18688894 DOI: 10.1002/Anie.200802296 |
0.334 |
|
| 2008 |
Laungani AC, Slattery JM, Krossing I, Breit B. Supramolecular bidentate ligands by metal-directed in situ formation of antiparallel beta-sheet structures and application in asymmetric catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 4488-502. PMID 18449870 DOI: 10.1002/Chem.200800359 |
0.34 |
|
| 2008 |
Šmejkal T, Breit B. A supramolecular catalyst for the decarboxylative hydroformylation of α,β-unsaturated carboxylic acids Angewandte Chemie - International Edition. 47: 3946-3949. PMID 18418816 DOI: 10.1002/Anie.200800956 |
0.312 |
|
| 2008 |
Usui I, Schmidt S, Keller M, Breit B. Allylation of N-heterocycles with allylic alcohols employing self-assembling palladium phosphane catalysts. Organic Letters. 10: 1207-10. PMID 18302396 DOI: 10.1021/Ol800073V |
0.366 |
|
| 2008 |
Smejkal T, Breit B. A supramolecular catalyst for regioselective hydroformylation of unsaturated carboxylic acids. Angewandte Chemie (International Ed. in English). 47: 311-5. PMID 17994656 DOI: 10.1002/Anie.200703192 |
0.354 |
|
| 2008 |
Breit B. Catalysts through self-assembly for combinatorial homogeneous catalysis Pure and Applied Chemistry. 80: 855-860. DOI: 10.1351/Pac200880050855 |
0.348 |
|
| 2008 |
Bruch A, Gebert A, Breit B. Tandem-directed regioselective hydroformylation/β-elimination: A practical method for the synthesis of enals Synthesis. 2169-2176. DOI: 10.1055/S-2008-1067140 |
0.349 |
|
| 2008 |
Bigot A, Breit B. A convenient allylic functionalization of bis(prop-2-enyl)methanol by direct trimetalation Synthesis. 3692-3696. DOI: 10.1055/S-0028-1083196 |
0.392 |
|
| 2008 |
Breit B. Directed rhodium-catalyzed hydroformylation of alkenes Topics in Organometallic Chemistry. 24: 145-168. DOI: 10.1007/3418_2007_067 |
0.321 |
|
| 2008 |
Šmejkal T, Breit B. Cover Picture: A Supramolecular Catalyst for Regioselective Hydroformylation of Unsaturated Carboxylic Acids (Angew. Chem. Int. Ed. 2/2008) Angewandte Chemie International Edition. 47: 219-219. DOI: 10.1002/Anie.200790258 |
0.351 |
|
| 2008 |
Šmejkal T, Breit B. Titelbild: A Supramolecular Catalyst for Regioselective Hydroformylation of Unsaturated Carboxylic Acids (Angew. Chem. 2/2008) Angewandte Chemie. 120: 225-225. DOI: 10.1002/Ange.200790258 |
0.354 |
|
| 2008 |
Kemme S, Šmejkal T, Breit B. Practical Synthesis of (E)-α,β-Unsaturated Carboxylic Acids Using a One-Pot Hydroformylation/Decarboxylative Knoevenagel Reaction Sequence Advanced Synthesis & Catalysis. 350: 1190-1190. DOI: 10.1002/Adsc.200890023 |
0.368 |
|
| 2008 |
Breit B. Dithioacetals as an Entry to Titanium-Alkylidene Chemistry: New and Efficient Carbonyl Olefination Organic Synthesis Set. 110-115. DOI: 10.1002/9783527620784.Ch17C |
0.368 |
|
| 2007 |
Spangenberg T, Schoenfelder A, Breit B, Mann A. A new method for the synthesis of chiral beta-branched alpha-amino acids. Organic Letters. 9: 3881-4. PMID 17803310 DOI: 10.1021/Ol071305M |
0.391 |
|
| 2007 |
Birkholz MN, Dubrovina NV, Jiao H, Michalik D, Holz J, Paciello R, Breit B, Börner A. Enantioselective hydrogenation with self-assembling rhodium phosphane catalysts: influence of ligand structure and solvent. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 5896-907. PMID 17429820 DOI: 10.1002/Chem.200601607 |
0.386 |
|
| 2007 |
Waloch C, Wieland J, Keller M, Breit B. Self-assembly of bidentate ligands for combinatorial homogeneous catalysis: methanol-stable platforms analogous to the adenine-thymine base pair. Angewandte Chemie (International Ed. in English). 46: 3037-9. PMID 17373012 DOI: 10.1002/Anie.200605202 |
0.355 |
|
| 2007 |
Reichert S, Breit B. Development of an axial chirality switch. Organic Letters. 9: 899-902. PMID 17284047 DOI: 10.1021/Ol0700660 |
0.385 |
|
| 2007 |
Spangenberg T, Schoenfelder A, Breit B, Mann A. Phosphine-Directed Diastereoselective Allylic Substitutions Synfacts. 2007: 1273-1273. DOI: 10.1055/S-2007-991379 |
0.433 |
|
| 2007 |
Šmejkal T, Breit B. Self-assembled bidentate ligands for ruthenium-catalyzed hydration of nitriles Organometallics. 26: 2461-2464. DOI: 10.1021/Om0611047 |
0.368 |
|
| 2007 |
Birkholz MN, Dubrovina NV, Shuklov IA, Holz J, Paciello R, Waloch C, Breit B, Börner A. Enantioselective Pd-catalyzed allylic amination with self-assembling and non-assembling monodentate phosphine ligands Tetrahedron Asymmetry. 18: 2055-2060. DOI: 10.1016/J.Tetasy.2007.08.026 |
0.417 |
|
| 2007 |
Stavrakov G, Keller M, Breit B. From central to axial to central chirality: Enantioselective construction of the trans-4,5,9,10-tetrahydroxy-9,10-dihydrophenanthrene system European Journal of Organic Chemistry. 5726-5733. DOI: 10.1002/Ejoc.200700583 |
0.435 |
|
| 2007 |
Breit B, Grünanger CU, Abillard O. Directed branched-regioselective hydroformylation of 2-substituted allylic o-DPPB esters European Journal of Organic Chemistry. 2497-2503. DOI: 10.1002/Ejoc.200700120 |
0.398 |
|
| 2007 |
Abillard O, Breit B. Domino hydroformylation/enantioselective cross-aldol addition Advanced Synthesis and Catalysis. 349: 1891-1895. DOI: 10.1002/Adsc.200700216 |
0.386 |
|
| 2006 |
Breit B, Demel P, Grauer D, Studte C. Stereospecific and stereodivergent construction of tertiary and quaternary carbon centers through switchable directed/nondirected allylic substitution. Chemistry, An Asian Journal. 1: 586-97. PMID 17441097 DOI: 10.1002/Asia.200600100 |
0.361 |
|
| 2006 |
Fuchs E, Keller M, Breit B. Phosphabarrelenes as ligands in rhodium-catalyzed hydroformylation of internal alkenes essentially free of alkene isomerization. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6930-9. PMID 16819735 DOI: 10.1002/Chem.200600180 |
0.395 |
|
| 2006 |
Demel P, Keller M, Breit B. o-DPPB-directed copper-mediated and -catalyzed allylic substitution with Grignard reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6669-83. PMID 16800021 DOI: 10.1002/Chem.200600225 |
0.382 |
|
| 2006 |
Herber C, Breit B. Iterative deoxypropionate synthesis based on a copper-mediated directed allylic substitution: formal total synthesis of borrelidin (C3-C11 fragment). Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 6684-91. PMID 16773665 DOI: 10.1002/Chem.200600343 |
0.456 |
|
| 2006 |
Weis M, Waloch C, Seiche W, Breit B. Self-assembly of bidentate ligands for combinatorial homogeneous catalysis: asymmetric rhodium-catalyzed hydrogenation. Journal of the American Chemical Society. 128: 4188-9. PMID 16568968 DOI: 10.1021/Ja058202O |
0.369 |
|
| 2006 |
Chevallier F, Breit B. Self-assembled bidentate ligands for Ru-catalyzed anti-Markovnikov hydration of terminal alkynes. Angewandte Chemie (International Ed. in English). 45: 1599-602. PMID 16447296 DOI: 10.1002/Anie.200503826 |
0.303 |
|
| 2006 |
Breit B, Fuchs E. Rhodium-Catalyzed Asymmetric Hydrogenation Synfacts. 2006: 1030-1030. DOI: 10.1055/S-2006-949318 |
0.337 |
|
| 2006 |
Breit B, Fuchs E. Chiral phosphabarrelene ligands: Synthesis and evaluation in rhodium-catalyzed asymmetric hydrogenation Synthesis. 2121-2128. DOI: 10.1055/S-2006-942425 |
0.416 |
|
| 2005 |
Breit B. Supramolecular approaches to generate libraries of chelating bidentate ligands for homogeneous catalysis. Angewandte Chemie (International Ed. in English). 44: 6816-25. PMID 16217817 DOI: 10.1002/Anie.200501798 |
0.329 |
|
| 2005 |
Herber C, Breit B. Enantioselective total synthesis and determination of the absolute configuration of the 4,6,8,10,16,18-hexamethyldocosane from Antitrogus parvulus. Angewandte Chemie (International Ed. in English). 44: 5267-9. PMID 16035027 DOI: 10.1002/Anie.200501612 |
0.407 |
|
| 2005 |
Breit B, Breuninger D. Practical synthesis of enantiomerically pure 2-(diphenylphosphanyl) ferrocene carboxylic acid Synthesis. 2782-2786. DOI: 10.1055/S-2005-872111 |
0.412 |
|
| 2005 |
Breit B, Breuninger D. Enantioselective copper-mediated allylic substitution with Grignard reagents employing a chiral reagent-directing leaving group Synthesis. 147-157. DOI: 10.1055/S-2004-831247 |
0.433 |
|
| 2005 |
Breit B, Zahn SK. Domino hydroformylation-Wittig olefination-hydrogenation Tetrahedron. 61: 6171-6179. DOI: 10.1016/J.Tet.2005.03.112 |
0.379 |
|
| 2005 |
Breit B, Breuninger D. Desymmetrizing hydroformylation of dialkenylcarbinols with the aid of a planar-chiral, catalyst-directing group European Journal of Organic Chemistry. 3916-3929. DOI: 10.1002/Ejoc.200500293 |
0.395 |
|
| 2005 |
Seiche W, Schuschkowski A, Breit B. Bidentate ligands by self-assembly through hydrogen bonding: A general room temperature/ambient pressure regioselective hydroformylation of terminal alkenes Advanced Synthesis and Catalysis. 347: 1488-1494. DOI: 10.1002/Adsc.200505174 |
0.364 |
|
| 2004 |
Breit B, Breuninger D. Desymmetrizing hydroformylation with the aid of a planar chiral catalyst-directing group. Journal of the American Chemical Society. 126: 10244-5. PMID 15315427 DOI: 10.1021/Ja0467364 |
0.391 |
|
| 2004 |
Breit B, Herber C. Iterative deoxypropionate synthesis based on a copper-mediated directed allylic substitution. Angewandte Chemie (International Ed. in English). 43: 3790-2. PMID 15258937 DOI: 10.1002/Anie.200453990 |
0.398 |
|
| 2004 |
Breit B, Demel P, Studte C. Stereospecific and stereodivergent construction of quaternary carbon centers through switchable directed/nondirected allylic substitution. Angewandte Chemie (International Ed. in English). 43: 3786-9. PMID 15258936 DOI: 10.1002/Anie.200453991 |
0.316 |
|
| 2004 |
Breit B, Fuchs E. Phosphabarrelene-rhodium complexes as highly active catalysts for isomerization free hydroformylation of internal alkenes. Chemical Communications (Cambridge, England). 694-5. PMID 15010785 DOI: 10.1039/B315709A |
0.365 |
|
| 2004 |
Breit B, Demel P, Gebert A. Directed regio- and stereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohols: a catalytic approach to the anti-aldol-retron. Chemical Communications (Cambridge, England). 114-5. PMID 14737358 DOI: 10.1039/B311378G |
0.337 |
|
| 2004 |
Quintard D, Keller M, Breit B. Practical synthesis of chlorosilyl-functionalized triphenylphosphanes Synthesis. 905-908. DOI: 10.1055/S-2004-816008 |
0.308 |
|
| 2004 |
Breit B, Demel P, Studte C. Stereospezifischer und stereodivergenter Aufbau quartärer Kohlenstoffzentren durch eine schaltbare dirigierte/nicht-dirigierte allylische Substitution Angewandte Chemie. 116: 3874-3877. DOI: 10.1002/Ange.200453991 |
0.364 |
|
| 2004 |
Breit B, Herber C. Iterative Desoxypropionat-Synthese auf der Basis einer kupfervermittelten dirigierten allylischen Substitution Angewandte Chemie. 116: 3878-3880. DOI: 10.1002/Ange.200453990 |
0.376 |
|
| 2003 |
Breit B, Seiche W. Hydrogen bonding as a construction element for bidentate donor ligands in homogeneous catalysis: regioselective hydroformylation of terminal alkenes. Journal of the American Chemical Society. 125: 6608-9. PMID 12769551 DOI: 10.1021/Ja0348997 |
0.363 |
|
| 2003 |
Breit B. Synthetic aspects of stereoselective hydroformylation. Accounts of Chemical Research. 36: 264-75. PMID 12693924 DOI: 10.1021/Ar0200596 |
0.446 |
|
| 2003 |
Breit B, Heckmann G, Zahn SK. Diastereoselective hydroformylation of 2-substituted allylic o-DPPB-esters-on the origin of 1,2-asymmetric induction. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 425-34. PMID 12532291 DOI: 10.1002/Chem.200390044 |
0.372 |
|
| 2003 |
Breit B, Laungani AC. Copper-catalyzed enantioselective conjugate addition of dialkylzinc reagents to enones with new peptidyl phosphane ligands Tetrahedron Asymmetry. 14: 3823-3826. DOI: 10.1016/J.Tetasy.2003.10.002 |
0.421 |
|
| 2002 |
al-Ktaifani MM, Bauer W, Bergsträsser U, Breit B, Francis MD, Heinemann FW, Hitchcock PB, Mack A, Nixon JF, Pritzkow H, Regitz M, Zeller M, Zenneck U. Hexaphosphapentaprismane: a new gateway to organophosphorus cage compound chemistry. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 2622-33. PMID 12180342 DOI: 10.1002/1521-3765(20020603)8:11<2622::Aid-Chem2622>3.0.Co;2-# |
0.514 |
|
| 2001 |
Breit B, Winde R, Mackewitz T, Paciello R, Harms K. Phosphabenzenes as monodentate pi-acceptor ligands for rhodium-catalyzed hydroformylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3106-21. PMID 11495438 DOI: 10.1002/1521-3765(20010716)7:14<3106::Aid-Chem3106>3.0.Co;2-Y |
0.375 |
|
| 2001 |
Breit B, Zahn SK. Stereoselective hydroformylation: key step for the assembly of polypropionate subunits. The Journal of Organic Chemistry. 66: 4870-7. PMID 11442419 DOI: 10.1021/Jo015634I |
0.384 |
|
| 2001 |
Breit B, Demel P. Copper‐Mediated and ‐Catalyzed o‐DPPB‐Directed Allylic Substitution Advanced Synthesis & Catalysis. 343: 429-432. DOI: 10.1002/1615-4169(200107)343:5<429::Aid-Adsc429>3.0.Co;2-K |
0.416 |
|
| 2001 |
Breit B, Zahn SK. Domino-Hydroformylierungs/Knoevenagel/Hydrierungs-Reaktion Angewandte Chemie. 113: 1964-1967. DOI: 10.1002/1521-3757(20010518)113:10<1964::Aid-Ange1964>3.0.Co;2-9 |
0.393 |
|
| 2000 |
Breit B, Zahn SK. Stereoselective hydroformylation, cuprate addition and domino reactions with the aid of a catalyst directing group Polyhedron. 19: 513-515. DOI: 10.1016/S0277-5387(99)00397-6 |
0.417 |
|
| 2000 |
Breit B. Controlling stereoselectivity with the aid of a reagent-directing group: Hydroformylation, cuprate addition, and domino reaction sequences Chemistry - a European Journal. 6: 1519-1524. DOI: 10.1002/(Sici)1521-3765(20000502)6:9<1519::Aid-Chem1519>3.3.Co;2-Y |
0.414 |
|
| 1999 |
Breit B, Zahn SK. Domino Hydroformylation-Wittig Reactions. Angewandte Chemie (International Ed. in English). 38: 969-971. PMID 29711852 DOI: 10.1002/(Sici)1521-3773(19990401)38:7<969::Aid-Anie969>3.0.Co;2-4 |
0.442 |
|
| 1999 |
Breit B. Probing new classes of π-acceptor ligands for rhodium catalyzed hydroformylation of styrene Journal of Molecular Catalysis a: Chemical. 143: 143-154. DOI: 10.1016/S1381-1169(98)00377-X |
0.389 |
|
| 1999 |
Breit B, Zahn SK. Domino-Hydroformylierungs-Wittig- Reaktionen Angewandte Chemie. 111: 1022-1024. DOI: 10.1002/(Sici)1521-3757(19990401)111:7<1022::Aid-Ange1022>3.0.Co;2-3 |
0.38 |
|
| 1998 |
Breit B. Dithioacetals as an Entry to Titanium-Alkylidene Chemistry: A New and Efficient Carbonyl Olefination. Angewandte Chemie (International Ed. in English). 37: 453-456. PMID 29711178 DOI: 10.1002/(Sici)1521-3773(19980302)37:4<453::Aid-Anie453>3.0.Co;2-M |
0.331 |
|
| 1998 |
Breit B. ortho-Diphenylphosphanylbenzoyl-Directed Cuprate Addition to Acyclic Enoates. Angewandte Chemie (International Ed. in English). 37: 525-527. PMID 29711161 DOI: 10.1002/(Sici)1521-3773(19980302)37:4<525::Aid-Anie525>3.0.Co;2-M |
0.37 |
|
| 1998 |
Breit B. Substrate-directed diastereoselective hydroaminomethylation of methallylic alcohols Tetrahedron Letters. 39: 5163-5166. DOI: 10.1016/S0040-4039(98)01038-7 |
0.331 |
|
| 1998 |
Breit B, Zahn SK. Diastereoselective hydroformylation of acyclic olefins: Efficient construction of an all-anti stereotriade building block for polyketide synthesis Tetrahedron Letters. 39: 1901-1904. DOI: 10.1016/S0040-4039(98)00158-0 |
0.331 |
|
| 1998 |
Breit B. ortho-Diphenylphosphanylbenzoyl-dirigierte Cuprat-Addition an acyclische Enoate Angewandte Chemie. 110: 535-538. DOI: 10.1002/(Sici)1521-3757(19980216)110:4<535::Aid-Ange535>3.0.Co;2-F |
0.378 |
|
| 1998 |
Breit B. 1,3-asymmetric induction in stereoselective rhodium-catalyzed hydroformylation of homomethallylic alcohols European Journal of Organic Chemistry. 1123-1134. DOI: 10.1002/(Sici)1099-0690(199806)1998:6<1123::Aid-Ejoc1123>3.0.Co;2-Y |
0.37 |
|
| 1997 |
Breit B, Winde R, Harms K. Phosphabenzene-rhodium catalysts for the efficient hydroformylation of terminal and internal olefins Journal of the Chemical Society - Perkin Transactions 1. 2681-2682. DOI: 10.1039/A705249I |
0.361 |
|
| 1997 |
Breit B. Substrate directed diastereoselective hydroformylation of acyclic homomethallylic alcohols Chemical Communications. 591-592. DOI: 10.1039/A608612H |
0.329 |
|
| 1997 |
Breit B. Substrate-directed diastereoselective hydroformylations, 1: Substrate-directed diastereoselective hydroformylation of methallylic alcohols - Development of an efficient catalyst-directing group for rhodium-catalyzed hydroformylation Liebigs Annales. 1841-1851. DOI: 10.1002/Jlac.199719970907 |
0.384 |
|
| 1997 |
Hoffmann A, Breit B, Regitz M. Organophosphorus Compounds, 114. Tetracyclic Phosphorus-Aluminium-Carbon Compounds – Synthesis by Cooligomerization of Kinetically Stabilized Phosphaalkynes with Trialkylaluminium Compounds Chemische Berichte. 130: 255-259. DOI: 10.1002/Cber.19971300219 |
0.521 |
|
| 1997 |
Mack A, Breit B, Wettling T, Bergsträsser U, Leininger S, Regitz M. Tetraphosphasemibullvalene: First Valence Isomerizations in the Phosphaalkyne Cyclotetramer System Angewandte Chemie (International Edition in English). 36: 1337-1340. DOI: 10.1002/Anie.199713371 |
0.415 |
|
| 1997 |
Mack A, Breit B, Wettling T, Bergsträßer U, Leininger S, Regitz M. Tetraphosphasemibullvalen: erste Valenzisomerisierungen im Phosphaalkin-Cyclotetramer-System Angewandte Chemie. 109: 1396-1398. DOI: 10.1002/Ange.19971091230 |
0.366 |
|
| 1997 |
Hoffmann A, Breit B, Regitz M. Tetracyclic phosphorus-aluminium-carbon compounds - Synthesis by cooligomerization of kinetically stabilized phosphaalkynes with trialkylaluminium compounds Chemische Berichte. 130: 255-259. |
0.388 |
|
| 1996 |
Regitz M, Weitling T, Fässler R, Breit B, Geissler B, Julino M, Hoffmann A, Bergsträsser U. Directed synthesis of phosphorus-carbon cage compounds - A challenge in organophosphorus chemistry [1] Phosphorus, Sulfur and Silicon and Related Elements. 109: 425-428. DOI: 10.1080/10426509608545181 |
0.505 |
|
| 1996 |
Breit B. Highly regioselective hydroformylation under mild conditions with new classes of π-acceptor ligands Chemical Communications. 2071-2072. DOI: 10.1039/Cc9960002071 |
0.38 |
|
| 1996 |
Breit B, Regitz M. Organophosphorus Compounds, 112. Lewis Acid Mediated Spirocyclotrimerization of Kinetically Stabilized Phosphaalkynes – Key Step for the Selective Generation and Trapping of Triphospha Dewar Benzenes Chemische Berichte. 129: 489-494. DOI: 10.1002/Cber.19961290504 |
0.544 |
|
| 1996 |
Breit B, Regitz M. Lewis acid mediated spirocyclotrimerization of phosphaalkynes -key step for the selective and of triphospfaa dewar benzenes Chemische Berichte. 129: 489-494. |
0.409 |
|
| 1995 |
Trost BM, Breit B, Peukert S, Zambrano J, Ziller JW. A New Platform for Designing Ligands for Asymmetric Induction in Allylic Alkylations Angewandte Chemie International Edition in English. 34: 2386-2388. DOI: 10.1002/Anie.199523861 |
0.704 |
|
| 1995 |
Trost BM, Breit B, Peukert S, Zambrano J, Ziller JW. Ein neues Konzept für das Design von chiralen Liganden für die asymmetrische Alkylierung von Allylverbindungen Angewandte Chemie. 107: 2577-2579. DOI: 10.1002/Ange.19951072114 |
0.632 |
|
| 1995 |
Trost BM, Breit B, Peukert S, Zambrano J, Ziller JW. A new platform for designing ligands for asymmetric induction in allylic alkylations Angewandte Chemie (International Edition in English). 34: 2386-2388. |
0.654 |
|
| 1994 |
Trost BM, Breit B, Organ MG. On the nature of the asymmetric induction in a palladium catalyzed allylic alkylation Tetrahedron Letters. 35: 5817-5820. DOI: 10.1016/S0040-4039(00)78192-5 |
0.695 |
|
| 1994 |
Breit B, Boese R, Regitz M. Organophosphorverbindungen LXXIII . Abfangreaktion eines "in situ" erzeugten Silens mit tBuCP. Bildung eines Diphosphatricyclobenzoheptans Journal of Organometallic Chemistry. 464: 41-45. DOI: 10.1016/0022-328X(94)87006-3 |
0.477 |
|
| 1994 |
Breit B, Hoffmann A, Bergsträsser U, Ricard L, Mathey F, Regitz M. The first carbon-phosphorus-aluminum cage compounds: Cyclooligomerization of phosphaalkynes with trialkylaluminum compounds Angewandte Chemie (International Edition in English). 33: 1491-1493. DOI: 10.1002/Anie.199414911 |
0.424 |
|
| 1994 |
Breit B, Hoffmann A, Bergsträßer U, Ricard L, Mathey F, Regitz M. Erste Kohlenstoff-Phosphor-Aluminium-Käfige; Cyclooligomerisierung von Phosphaalkinen mit Trialkylaluminium-Verbindungen Angewandte Chemie. 106: 1541-1543. DOI: 10.1002/Ange.19941061416 |
0.411 |
|
| 1993 |
Regitz M, Wettling T, Breit B, Birkel M, Geissler B, Bergstrasser U, Barth S, Binger P. The mediated cyclooligomerization of phosphaalkynes - new aspects in the synthesis of polycyclic phosphorus compounds [1] Phosphorus, Sulfur, and Silicon and the Related Elements. 76: 1-4. DOI: 10.1080/10426509308032343 |
0.432 |
|
| 1993 |
Breit B, Regitz M. Organophorphorus compounds; 65. The phospha-ane reaction: An unusual dimerization of phosphaalkenes Synthesis. 285-287. DOI: 10.1055/S-1993-25847 |
0.484 |
|
| 1993 |
Breit B, Regitz M. Organophosphorverbindungen, 71[1]. Phosphaalkine und Phosphaalkene als Abfangpartner für 1,2-Dehydrobenzol und Phenylium-2-carboxylat[2] Chemische Berichte. 126: 1945-1950. DOI: 10.1002/Cber.19931260826 |
0.506 |
|
| 1992 |
Breit B, Memmesheimer H, Boese R, Regitz M. Organophosphorverbindungen, 53[1] Cyclopropenyliden-methylen-diphosphane – neue gekreuzt konjugierte Phosphapolyene[2] Chemische Berichte. 125: 729-732. DOI: 10.1002/Cber.19921250328 |
0.469 |
|
| 1992 |
Breit B, Bergsträsser U, Maas G, Regitz M. Spirocyclization of a stable phosphaalkyne with aluminum trichloride - Key reaction for the production of triphospha dewar benzene derivatives Angewandte Chemie (International Edition in English). 31: 1055-1058. DOI: 10.1002/Anie.199210551 |
0.515 |
|
| 1992 |
Breit B, Bergsträßer U, Maas G, Regitz M. Spirocyclotrimerisierung eines stabilen Phosphaalkins mit Aluminiumtrichlorid - Schlüsselreaktion zur Erzeugung von Triphospha-Dewar-Benzolderivaten Angewandte Chemie. 104: 1043-1046. DOI: 10.1002/Ange.19921040812 |
0.402 |
|
| 1991 |
Fuchs E, Breit B, Bergstrasser U, Hoffmann J, Heydt H, Regitz M. Organophosphorus compounds; 52. Phosphatriafulvenes and their reactions with electrophiles Synthesis. 1099-1107. DOI: 10.1055/S-1991-28399 |
0.487 |
|
| 1991 |
Fuchs E, Breit B, Heydt H, Regitz M, Schoeller W, Busch T, Krüger C, Betz P. Organophosphorverbindungen, 511) Phosphatriafulvene – Phosphaalkene mit inverser Elektronendichte2) Chemische Berichte. 124: 2843-2855. DOI: 10.1002/Cber.19911241228 |
0.462 |
|
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