| Year |
Citation |
Score |
| 2010 |
Boche G. ChemInform Abstract: Carbenoids, Nitrenoids, and Oxenoids: Very Electrophilic “Anions” Cheminform. 30: no-no. DOI: 10.1002/CHIN.199924310 |
0.277 |
|
| 2010 |
EDWARDS C, BOCHE G, STEINBRECHER T, SCHEER S. ChemInform Abstract: Synthesis of 2-Substituted 2′-Deoxyguanosines and 6-O-Allylguanines via the Activation of C-2 by a Trifluoromethanesulfonate Group. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199745250 |
0.285 |
|
| 2010 |
BOCHE G, LOHRENZ JCW, OPEL A. ChemInform Abstract: From “Carbanions” to Carbenoids: The Structure of Lithiated Amines and Lithiated Ethers Cheminform. 26: no-no. DOI: 10.1002/CHIN.199552300 |
0.31 |
|
| 2010 |
BOCHE G, HALLER F, HARMS K, HOPPE D, KOCH W, LOHRENZ J, MARSCH M, OPEL A, THUEMMLER C, ET AL. EA. ChemInform Abstract: Crystal Structure and Reactivity (Selectivity) of Oxygen (Aryloxy-, Carbamoyloxy-, Silyloxy) -Substituted Lithium Compounds Cheminform. 26: no-no. DOI: 10.1002/chin.199526280 |
0.298 |
|
| 2010 |
PYNE SG, BOCHE G. ChemInform Abstract: Chiral Sulfur Compounds. Part 21. Synthesis and Conjugate 1,2-Addition Reactions of a Sterically Hindered Allylic Sulfoximine. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199402064 |
0.322 |
|
| 2010 |
ZARGES W, MARSCH M, HARMS K, KOCH W, FRENKING G, BOCHE G. ChemInform Abstract: Crystal Structure of α-(Trimethylsilyl)benzyllithium× Tetramethylethylenediamine (C6H5CH(SiMe3)Li×TMEDA) and α-( Phenylthio)benzyllithium×3 Tetrahydrofuran (C6H5CH(SPh)Li×( THF)3) - Two Benzyllithium Compounds with Central Chirality. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199122041 |
0.305 |
|
| 2010 |
Boche G, Lohrenz JCW, Cioslowski J, Koch W. Carbon acidity resulting from sulfur substituents The Chemistry of Sulphur-Containing Functional Groups. 339-362. DOI: 10.1002/9780470034408.ch7 |
0.224 |
|
| 2006 |
Bickelhaupt FM, Hermann HL, Boche G. Alpha-stabilization of carbanions: fluorine is more effective than the heavier halogens. Angewandte Chemie (International Ed. in English). 45: 823-6. PMID 16365915 DOI: 10.1002/Anie.200501633 |
0.307 |
|
| 2006 |
Bickelhaupt FM, Hermann HL, Boche G. α-Stabilisierung von Carbanionen: Fluor übertrifft die schwereren Halogene Angewandte Chemie. 118: 838-841. DOI: 10.1002/Ange.200501633 |
0.347 |
|
| 2006 |
Boche G. Chemical Carcinogens. Activation Mechanisms, Structural and Electronic Factors, and Reactivity. Bioactive Molecules Series, Vol. 5 Herausgegeben von P. Politzer und F. J. Martin Jr. Elsevier, Amsterdam 1988. XIV, 366 S., geb. Hfl 280.00. – ISBN 0-444-43008-3 Angewandte Chemie. 101: 1098-1099. DOI: 10.1002/Ange.19891010845 |
0.347 |
|
| 2005 |
Adler M, Adler S, Boche G. Tetrahedral intermediates in reactions of carboxylic acid derivatives with nucleophiles Journal of Physical Organic Chemistry. 18: 193-209. DOI: 10.1002/Poc.807 |
0.408 |
|
| 2004 |
Haack T, Boche G, Kliem C, Wiessler M, Albert D, Schmeiser HH. Synthesis, characterization, and 32P-postlabeling of N-(deoxyguanosin)-4-aminobiphenyl 3'-phosphate adducts. Chemical Research in Toxicology. 17: 776-84. PMID 15206898 DOI: 10.1021/Tx0342666 |
0.372 |
|
| 2003 |
Deberitz J, Boche G. Lithium und seine Verbindungen ‐ Industrielle, medizinische und wissenschaftliche Bedeutung Chemie in Unserer Zeit. 37: 258-266. DOI: 10.1002/Ciuz.200300264 |
0.389 |
|
| 2002 |
Glende C, Klein M, Schmitt H, Erdinger L, Boche G. Transformation of mutagenic aromatic amines into non-mutagenic species by alkyl substituents. Part II: alkylation far away from the amino function. Mutation Research. 515: 15-38. PMID 11909752 DOI: 10.1016/S1383-5718(01)00345-X |
0.389 |
|
| 2002 |
Kocieński P, Marsch M, Harms K, Boche G. A vinylic α-carbamoyloxyborane with a carbenoid-type bonding arrangement Acta Crystallographica Section E Structure Reports Online. 58: o336-o337. DOI: 10.1107/S1600536802003215 |
0.403 |
|
| 2001 |
Hermann HL, Boche G, Schwerdtfeger P. Metallophilic interactions in closed-shell copper(I) compounds--a theoretical study. Chemistry: a European Journal. 7: 5333-5342. PMID 11822433 DOI: 10.1002/1521-3765(20011217)7:24<5333::Aid-Chem5333>3.0.Co;2-1 |
0.342 |
|
| 2001 |
Boche G, Lohrenz JCW. The electrophilic nature of carbenoids, nitrenoids, and oxenoids. Chemical Reviews. 101: 697-756. PMID 11712501 DOI: 10.1021/Cr940260X |
0.326 |
|
| 2001 |
Glende C, Schmitt H, Erdinger L, Engelhardt G, Boche G. Transformation of mutagenic aromatic amines into non-mutagenic species by alkyl substituents. Part I. Alkylation ortho to the amino function. Mutation Research. 498: 19-37. PMID 11673068 DOI: 10.1016/S1383-5718(01)00259-5 |
0.414 |
|
| 2001 |
Gschwind RM, Xie X, Rajamohanan PR, Auel C, Boche G. Me(2)CuLi*LiCN in diethyl ether prefers a homodimeric core structure [Me(2)CuLi](2) and not a heterodimeric one [Me(2)CuLi*LiCN]: (1)H, (6)Li HOE and (1)H, (1)H NOE studies by NMR. Journal of the American Chemical Society. 123: 7299-7304. PMID 11472157 DOI: 10.1021/Ja004350X |
0.373 |
|
| 2001 |
Ludolph B, Klein M, Erdinger L, Boche G. The effects of 4'-alkyl substituents on the mutagenic activity of 4-amino- and 4-nitrostilbenes in Salmonella typhimurium. Mutation Research-Genetic Toxicology and Environmental Mutagenesis. 491: 195-209. PMID 11287312 DOI: 10.1016/S1383-5718(01)00142-5 |
0.395 |
|
| 2001 |
Haack T, Erdinger L, Boche G. Mutagenicity in Salmonella typhimurium TA98 and TA100 of nitroso and respective hydroxylamine compounds Mutation Research-Genetic Toxicology and Environmental Mutagenesis. 491: 183-193. PMID 11287311 DOI: 10.1016/S1383-5718(01)00140-1 |
0.38 |
|
| 2001 |
Bosold F, Marsch M, Harms Κ, Boche G. Crystal structure of (3THF)-N-lithiium-N-(2',4',6'-tris-t-butyl-phenyl)-E'pentene(1)-amide,C35H62LiNO3 Zeitschrift Fur Kristallographie-New Crystal Structures. 216: 449-450. DOI: 10.1524/Ncrs.2001.216.14.449 |
0.395 |
|
| 2001 |
Hassani K, Marsch M, Harms Κ, Boche G. Crystal structure of 2-(1,3-dimethylbenzotriazolium) nickeltetrabromide, (C8H10N3)2NiBr4 Zeitschrift Fur Kristallographie-New Crystal Structures. 216: 447-448. DOI: 10.1524/Ncrs.2001.216.14.447 |
0.359 |
|
| 2001 |
Demyanov P, Marsch M, Harms K, Boche G. Crystal structure of (2PMDETA)-dilithium-1-(cyclononatetraenyl)- enolate, C29H56Li2N6O Zeitschrift Fur Kristallographie-New Crystal Structures. 216: 445-446. DOI: 10.1524/Ncrs.2001.216.14.445 |
0.362 |
|
| 2001 |
Bosold F, Marsch M, Harms Κ, Boche G. Crystal structure of bis[bis(diethylether)lithium (trimethylsilyl)methyl-cyanocuprate], [(C4H10O)2Li(C3H9)SiCH2CuCN]2 Zeitschrift Fur Kristallographie-New Crystal Structures. 216: 143-144. DOI: 10.1524/Ncrs.2001.216.14.143 |
0.391 |
|
| 2001 |
Boche G, Ledig B, Marsch M, Harms K. [Indenyllithium·2(N,N,N′-trimethylethylenediamine)]∞: N–H hydrogen bridges to the indenyl anion Acta Crystallographica Section E-Structure Reports Online. 57. DOI: 10.1107/S1600536801018876 |
0.417 |
|
| 2001 |
Möller M, Husemann M, Boche G. Oxidation of organometallic compounds (RM, M = Li, MgBr, ZnBr, CuCNLi, Cu(R)CNLi2) with tBuOOLi, Ti(OiPr)4-mediated with tBuOOH, and with O2, to give alcohols (ROH). Are radicals R• involved? Journal of Organometallic Chemistry. 624: 47-52. DOI: 10.1016/S0022-328X(00)00596-9 |
0.39 |
|
| 2001 |
Boche G. Book Review: Modern Amination Methods. Edited by Alfredo Ricci. Angewandte Chemie. 40: 1315-1316. DOI: 10.1002/1521-3773(20010401)40:7<1315::Aid-Anie1315>3.0.Co;2-W |
0.304 |
|
| 2001 |
Boche G. Buchbesprechung: Modern Amination Methods. Herausgegeben von Alfredo Ricci. Angewandte Chemie. 113: 1355-1356. DOI: 10.1002/1521-3757(20010401)113:7<1355::Aid-Ange1355>3.0.Co;2-0 |
0.317 |
|
| 2001 |
Jänsch H, Kannenberg S, Boche G. Sulfonated Diphenylphosphanes for Homogeneous Biphasic Catalysis via a Combined Protection/Deprotection Protocol European Journal of Organic Chemistry. 2001: 2923-2926. DOI: 10.1002/1099-0690(200108)2001:15<2923::Aid-Ejoc2923>3.0.Co;2-I |
0.355 |
|
| 2000 |
John M, Auel C, Behrens C, Marsch M, Harms K, Bosold F, Gschwind RM, Rajamohanan PR, Boche G. The relation between ion pair structures and reactivities of lithium cuprates Chemistry: a European Journal. 6: 3060-3068. PMID 10993267 DOI: 10.1002/1521-3765(20000818)6:16<3060::Aid-Chem3060>3.0.Co;2-M |
0.418 |
|
| 2000 |
Klein M, Erdinger L, Boche G. From mutagenic to non-mutagenic nitroarenes: effect of bulky alkyl substituents on the mutagenic activity of nitroaromatics in Salmonella typhimurium. Part II. Substituents far away from the nitro group. Mutation Research-Genetic Toxicology and Environmental Mutagenesis. 467: 69-82. PMID 10771272 DOI: 10.1016/S1383-5718(00)00013-9 |
0.404 |
|
| 2000 |
Klein M, Voigtmann U, Haack T, Erdinger L, Boche G. From mutagenic to non-mutagenic nitroarenes: effect of bulky alkyl substituents on the mutagenic activity of 4-nitrobiphenyl in Salmonella typhimurium. Part I. Substituents ortho to the nitro group and in 2'-position. Mutation Research. 467: 55-68. PMID 10771271 DOI: 10.1016/S1383-5718(00)00012-7 |
0.296 |
|
| 2000 |
Gschwind RM, Rajamohanan PR, John M, Boche G. Direct Insight into the Ion Pair Equilibria of Lithium Organocuprates by 1H,6Li HOESY Experiments Organometallics. 19: 2868-2873. DOI: 10.1021/Om000068N |
0.401 |
|
| 2000 |
Hermann H, Lohrenz JCW, Kühn A, Boche G. The Influence of the Leaving Group X (X=F, Cl, Br, I, OH) on the Carbenoid Nature of the Carbenoids LiCH 2 X and XZnCH 2 X—A Theoretical Study Tetrahedron. 56: 4109-4115. DOI: 10.1016/S0040-4020(00)00334-3 |
0.364 |
|
| 1999 |
Adler M, Marsch M, Nudelman NS, Boche G. [(Ph) (NMe )C(OLi)⋅THF] : Crystal Structure of the Tetrahedral Intermediate Formed in the Reaction of N,N-Dimethylbenzamide and Phenyllithium. Angewandte Chemie (International Ed. in English). 38: 1261-1263. PMID 29711747 DOI: 10.1002/(Sici)1521-3773(19990503)38:9<1261::Aid-Anie1261>3.0.Co;2-E |
0.415 |
|
| 1999 |
Ledig B, Marsch M, Harms K, Boche G. Crystal structure of (1-cyano-indenyl-N-((-)spateine-N,N')- (tetrafuran-O)-lithium, C29H40LiN3O Zeitschrift Fur Kristallographie-New Crystal Structures. 214: 511-512. DOI: 10.1515/Ncrs-1999-0456 |
0.396 |
|
| 1999 |
Langlotz I, Marsch M, Harms K, Boche G. Crystal structure of (benzylcyano-N)-(1,4,7,10-tetraoxocyclodecane-O,O',O'',O''')-lithium, C~16~H~22~LiNO~4~ Zeitschrift Fur Kristallographie-New Crystal Structures. 214: 509-510. DOI: 10.1515/Ncrs-1999-0455 |
0.371 |
|
| 1999 |
Klein M, Boche G. Regiospecific Synthesis of Substituted Nitrofluorenes and Aminofluorenes with the Negishi Coupling Reaction as Key Step Synthesis. 1999: 1246-1250. DOI: 10.1055/S-1999-3537 |
0.38 |
|
| 1999 |
Myshakin EM, Boche G, Petrosyan VS, Alekseiko LN, Gory L, Moscow. Ab Initio MO and Density Functional Theory Study of Substituent Effects on Electron Attachment to Benzyl Chlorides Journal of Physical Chemistry A. 103: 11469-11473. DOI: 10.1021/Jp993043E |
0.398 |
|
| 1999 |
Adler M, Marsch M, Nudelman NS, Boche G. [(Ph)2(NMe2)C(OLi)⋅THF]2: Kristallstruktur der tetraedrischen Zwischenstufe aus der Umsetzung von Benzoesäuredimethylamid mit Phenyllithium Angewandte Chemie. 111: 1345-1347. DOI: 10.1002/(Sici)1521-3757(19990503)111:9<1345::Aid-Ange1345>3.0.Co;2-W |
0.374 |
|
| 1998 |
Boche G, Bosold F, Marsch M, Harms K. The Crystal Structures of a Lower Order and a "Higher Order" Cyanocuprate: [tBuCu(CN)Li(OEt ) ] and [tBuCutBu{Li(thf)(pmdeta)} CN]. Angewandte Chemie (International Ed. in English). 37: 1684-1686. PMID 29711526 DOI: 10.1002/(Sici)1521-3773(19980703)37:12<1684::Aid-Anie1684>3.0.Co;2-2 |
0.372 |
|
| 1998 |
Bosold F, Marsch M, Harms K, Boche G. Crystal structure of bis(1-lithio-1,2-diphenylhydrazine)-1,2-dilithio- 1,2-diphenylhydrazine-tetrakis(diethyl ether), [(C6H5)2N2Li]2[(C6H5)2N2Li2](C4H10O)4 Zeitschrift Fur Kristallographie-New Crystal Structures. 213: 651-652. DOI: 10.1524/Ncrs.1998.213.14.651 |
0.359 |
|
| 1998 |
Bosold F, Marsch M, Harms K, Boche G. Crystal structure of 1-lithio-1-phenyl-2,2-dimethylhydrazinetetrahydrofuran, [(C6H5)(CH3)2N2]Li·C4H8O Zeitschrift Fur Kristallographie-New Crystal Structures. 213: 649-650. DOI: 10.1524/Ncrs.1998.213.14.649 |
0.368 |
|
| 1998 |
Bosold F, Marsch M, Harms K, Boche G. Crystal structure of 1-lithio-1-phenyl-2,2-dimethylhydrazine-pentamethyldiethylenetriamine, [(C6H5)(CH3)2N2]Li(C9H23N3) Zeitschrift Fur Kristallographie-New Crystal Structures. 213: 647-648. DOI: 10.1524/Ncrs.1998.213.14.647 |
0.374 |
|
| 1998 |
Robert M, Neudeck A, Boche G, Willeke C, Rangappa KS, Andrews P. Electron transfer chemistry of some unusual nitrogen compounds: from stable nitrenium ions to the corresponding nitrogen centered radicals New Journal of Chemistry. 22: 1437-1444. DOI: 10.1039/A805657I |
0.355 |
|
| 1998 |
Wüllner G, Jänsch H, Schubert F, Boche G. Palladium-catalyzed amination of aromatic halides in water-containing solvent systems: a two-phase protocol Chemical Communications. 1509-1510. DOI: 10.1039/A803819H |
0.334 |
|
| 1998 |
Nudelman NS, Schulz H, Liñares GG, Bonatti A, Boche G. Further Insights into the Chemistry of Acyllithium Compounds R2NC(O)Li: Characterization of an Amide (R2NLi) Adduct (R2NCHNR2(OLi)) to a Formamide (R2NC(O)H) Organometallics. 17: 146-150. DOI: 10.1021/Om970293D |
0.45 |
|
| 1998 |
Cioslowski J, Piskorz P, Schimeczek M, Boche G. Diversity of bonding in methyl ate anions of the first- and second-row elements Journal of the American Chemical Society. 120: 2612-2615. DOI: 10.1021/Ja972564H |
0.347 |
|
| 1998 |
Schade S, Boche G. The effect of (poly)amine ligands on the solution structure of [6Li]-α-(phenylthio)benzyllithium in tetrahydrofuran: A 1H,6Li-HOESY NMR study1Dedicated to Professor Ken Wade on the occasion of his 65th birthday.1 Journal of Organometallic Chemistry. 550: 359-379. DOI: 10.1016/S0022-328X(97)00239-8 |
0.414 |
|
| 1998 |
Boche G. Carbenoids, nitrenoids, oxenoids: Very electrophilic „anions” Macromolecular Symposia. 134: 1-12. DOI: 10.1002/Masy.19981340103 |
0.404 |
|
| 1998 |
Boche G, Bosold F, Hermann H, Marsch M, Harms K, Lohrenz JCW. Crystal Structure of [2‐ZnCl‐benzoxazole⋅2 THF]2: The Remarkable Difference between 2‐ZnHal‐ and 2‐Li‐oxazoles Chemistry: a European Journal. 4: 814-817. DOI: 10.1002/(Sici)1521-3765(19980515)4:5<814::Aid-Chem814>3.0.Co;2-F |
0.328 |
|
| 1998 |
Boche G, Bosold F, Marsch M, Harms K. Die Kristallstrukturen eines Lower‐order‐ und eines „Higher‐order”︁‐Cyanocuprates: [tBuCu(CN)Li(OEt2)2]∞ und [tBuCutBu{Li(thf)(pmdeta)2CN}] Angewandte Chemie. 110: 1779-1781. DOI: 10.1002/(Sici)1521-3757(19980619)110:12<1779::Aid-Ange1779>3.0.Co;2-8 |
0.363 |
|
| 1998 |
Boche G, Schimeczek M, Cioslowski J, Piskorz P. The role of ate complexes in halogen(metalloid)-metal exchange reactions: A theoretical study European Journal of Organic Chemistry. 1851-1860. DOI: 10.1002/(Sici)1099-0690(199809)1998:9<1851::Aid-Ejoc1851>3.0.Co;2-N |
0.419 |
|
| 1998 |
Enders D, Kirchhoff J, Gerdes P, Mannes D, Raabe G, Runsink J, Boche G, Marsch M, Ahlbrecht H, Sommer H. Structure and Reactivity of Lithiated α-Amino Nitriles European Journal of Organic Chemistry. 1998: 63-72. DOI: 10.1002/(Sici)1099-0690(199801)1998:1<63::Aid-Ejoc63>3.0.Co;2-H |
0.388 |
|
| 1997 |
Hilf C, Bosold F, Harms K, Marsch M, Boche G. The Equilibrium Between 2-Lithium-Oxazole(-Thiazole, -Imidazole) Derivatives and Their Acyclic Isomers – A Structural Investigation† Chemische Berichte. 130: 1213-1221. DOI: 10.1002/Cber.19971300908 |
0.432 |
|
| 1997 |
Hill C, Bosold F, Harms K, Lohrenz JCW, Marsch M, Schmieczek M, Boche G. Carbene Structure Of Stable Acyl (Formyl) Anion Equivalents Chemische Berichte. 130: 1201-1212. DOI: 10.1002/Cber.19971300907 |
0.421 |
|
| 1997 |
Schalley CA, Schröder D, Schwarz H, Möbus K, Boche G. On the oxenoid character of alkylperoxy anions and their lithium compounds: A combined mass-spectrometric and theoretical investigation Chemische Berichte. 130: 1085-1097. DOI: 10.1002/Cber.19971300810 |
0.383 |
|
| 1997 |
Cioslowski J, Boche G. Geometry-Tunable Lewis Acidity of Amidinium Cations and Its Relevance to Redox Reactions of the Thauer Metal-Free Hydrogenase: A Theoretical Study Angewandte Chemie (International Edition in English). 36: 107-109. DOI: 10.1002/Anie.199701071 |
0.365 |
|
| 1997 |
Cioslowski J, Boche G. Konformationsgesteuerte Lewis-Acidität von Amidinium-Ionen und ihre Bedeutung für die Redoxreaktionen der Thauerschen metallfreien Hydrogenase – eine theoretische Studie Angewandte Chemie. 109: 165-167. DOI: 10.1002/Ange.19971090155 |
0.369 |
|
| 1996 |
Boche G, Möbus K, Harms K, Lohrenz JCW, Marsch M. [Lithium tert-butylperoxide]12 : Crystal Structure of an Aggregated Oxenoid. Chemistry (Weinheim An Der Bergstrasse, Germany). 2: 604-607. PMID 29178227 DOI: 10.1002/Chem.19960020521 |
0.412 |
|
| 1996 |
Boche G, Willeke C, Marsch M, Harms K. Crystal structure of 1,3-dibenzyl-1,2,3-triazolium iodide, (C6H5CH2)2(C2H2N3)+I- Zeitschrift Fur Kristallographie. 211: 583-584. DOI: 10.1524/Zkri.1996.211.8.583 |
0.367 |
|
| 1996 |
Boche G, Rangappa K, Harms K, Marsch M. Crystal structure of 1-benzyl-3-methyl-1,2,3-triazolium Perchlorate, (C6H5)(N3C3H7)+ClO4- Zeitschrift Fur Kristallographie. 211: 581-582. DOI: 10.1524/Zkri.1996.211.8.581 |
0.369 |
|
| 1996 |
Hoppe I, Hoppe D, Marsch M, Harms K, Boche G. Crystal structure of (1R)-1-methyl-1-(α-methylbenzyl-carboxamido)-indene, C19H19NO Zeitschrift FüR Kristallographie - Crystalline Materials. 211. DOI: 10.1524/Zkri.1996.211.5.331 |
0.375 |
|
| 1996 |
Boche G, Möbus K, Harms K, Marsch M. [((η2-tert-Butylperoxo)titanatrane)2· 3 Dichloromethane]: X-ray Crystal Structure and Oxidation Reactions Journal of the American Chemical Society. 118: 2770-2771. DOI: 10.1021/Ja954308F |
0.382 |
|
| 1996 |
Boche G, Andrews P, Harms K, Marsch M, Rangappa KS, Schimeczek M, Willeke C. Crystal and electronic structure of stable nitrenium ions. A comparison with structurally related carbenes Journal of the American Chemical Society. 118: 4925-4930. DOI: 10.1021/Ja9536274 |
0.377 |
|
| 1996 |
Boche G. Karl Dimroth: 18. 8. 1910 – 26. 11. 1995 Chemie in Unserer Zeit. 30: 45-45. DOI: 10.1002/Ciuz.19960300108 |
0.322 |
|
| 1996 |
Jaenicke L, König H, Herberhold M, Boche G, Wambach H, Hensel F, Janoschek R. Chemie in 30 Jahren Chemie in Unserer Zeit. 30: 39-44. DOI: 10.1002/Ciuz.19960300107 |
0.345 |
|
| 1996 |
Müller A, Marsch M, Harms K, Lohrenz JCW, Boche G. LiCHCl2 · 3 Pyridine, Structure of a Carbenoid with a Tetrahedral C Atom Angewandte Chemie. 35: 1518-1520. DOI: 10.1002/Anie.199615181 |
0.36 |
|
| 1996 |
Müller A, Marsch M, Harms K, Lohrenz JCW, Boche G. LiCHCl2 · 3 Pyridin, Struktur eines Carbenoids mit tetraedrischem C‐Atom im Kristall Angewandte Chemie. 108: 1639-1640. DOI: 10.1002/Ange.19961081328 |
0.375 |
|
| 1995 |
Scheer S, Steinbrecher T, Boche G. A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. Environmental Health Perspectives. 151-2. PMID 7889838 DOI: 10.1289/EHP.94102S6151 |
0.315 |
|
| 1995 |
Dem'yanov P, Boche G, Marsch M, Harms K, Fyodorova G, Petrosyan V. Crystal Structure of η3‐lithio‐1,3,3‐triphenylpropyne‐(diethyl ether)2 and [1‐lithio‐1‐(2‐methoxyphenyl)‐3,3‐diphenylallene–diethyl ether]2: Propargyl‐ versus allenyl‐type structures Liebigs Annalen. 1995: 457-460. DOI: 10.1002/Jlac.199519950361 |
0.39 |
|
| 1995 |
Ruhland T, Hoffmann RW, Schade S, Boche G. Chiral Organometallic Reagents, XIII. Structural Aspects of Differentially Solvated Benzyllithium Contact Ion Pairs Chemische Berichte. 128: 551-556. DOI: 10.1002/Cber.19951280604 |
0.407 |
|
| 1995 |
Hoppe I, Marsch M, Harms K, Boche G, Hoppe D. Generation of Enantiomerically Enriched Lithium Indenides by Means of (–)‐Sparteine: Structure, Stereoselective Substitution, and Solvent Effects Angewandte Chemie. 34: 2158-2160. DOI: 10.1002/Anie.199521581 |
0.413 |
|
| 1995 |
Boche G, Hilf C, Harms K, Marsch M, Lohrenz JCW. Crystal Structure of the Dimeric (4‐tert‐Butylthiazolato)(glyme)lithium: Carbene Character of a Formyl Anion Equivalent Angewandte Chemie. 34: 487-489. DOI: 10.1002/Anie.199504871 |
0.401 |
|
| 1995 |
Hoppe I, Hoppe D, Boche G, Marsch M, Harms K. Bildung von enantiomerenangereicherten Lithiumindeniden mit (−)-Spartein — Strukturen, stereospezifische Substitution, Einfluß des Lösungsmittels Angewandte Chemie. 107: 2328-2330. DOI: 10.1002/Ange.19951071926 |
0.378 |
|
| 1995 |
Boche G, Hilf C, Harms K, Marsch M, Lohrenz JCW. Struktur des dimeren (4‐tert‐Butyl‐thiazolato)(glyme)lithiums: Carben‐Charakter eines Formyl‐Anion‐Äquivalents Angewandte Chemie. 107: 509-511. DOI: 10.1002/Ange.19951070420 |
0.373 |
|
| 1994 |
Boche G, Harms K, Marsch M, Müller A. 9-Bromo-9-[(bromomagnesium)methylene]fluorene–tetrahydrofuran (1/4) structure of a MgBr/Br carbenoid Journal of the Chemical Society, Chemical Communications. 1393-1394. DOI: 10.1039/C39940001393 |
0.408 |
|
| 1994 |
Boche G, Lohrenz JCW, Schubert F. Lithio-diazomethane and lithio-(trimethylsilyl)diazomethane: Theoretical and experimental studies of their structures, reactions and reaction products Tetrahedron. 50: 5889-5902. DOI: 10.1016/S0040-4020(01)90444-2 |
0.446 |
|
| 1994 |
Boche G, Langlotz I, Marsch M, Harms K. X‐Ray Crystal Structures of the Enolate of tert‐Butyl α‐Cyanoacetate with Li+ or Protonated 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU‐H+) as Gegenion. N—H Hydrogen Bridge from DBU‐H+ to the Enolate Oxygen Atom Chemische Berichte. 127: 2059-2064. DOI: 10.1002/Cber.19941271031 |
0.413 |
|
| 1994 |
Boche G, Harms K, Marsch M, Schubert F. {6 Lithio(trimethylsilyl)diazomethane· 2 Lithio[4,5‐bis(trimethylsilyl)triazene]· 7 Diethyl Ether}: The First X‐Ray Structure Analysis of a Lithiated Diazoalkane Chemische Berichte. 127: 2193-2195. DOI: 10.1002/Cber.1491271118 |
0.437 |
|
| 1994 |
Boche G, Bosold F, Lohrenz JCW. The Oxenoid Character of Metalated Hydroperoxides O(M)OR: Oxidation of Organometallic Compounds R′M′ to R′OH under Mild Conditions Angewandte Chemie. 33: 1161-1163. DOI: 10.1002/Anie.199411611 |
0.352 |
|
| 1994 |
Boche G, Boie C, Bosold F, Harms K, Marsch M. [(N-Lithio-N-mesitylsulfonyloxy-tert-butylcarbamate)2·(thf)3]: Crystal Structure of a Nitrenoid† Angewandte Chemie. 33: 115-117. DOI: 10.1002/Anie.199401151 |
0.394 |
|
| 1994 |
Boche G, Bosold F, Lohrenz JCW. Der oxenoide Charakter metallierter Hydroperoxide O(M)OR: Oxidation von metallorganischen Verbindungen R′M′ zu R′OH unter milden Bedingungen Angewandte Chemie. 106: 1228-1230. DOI: 10.1002/Ange.19941061114 |
0.333 |
|
| 1994 |
Boche G, Boie C, Bosold F, Harms K, Marsch M. [(N‐Lithio‐N‐mesitylsulfonyloxy‐tert‐butylcarbamat)2 · (thf)3]: Struktur eines Nitrenoids im Kristall Angewandte Chemie. 106: 90-91. DOI: 10.1002/Ange.19941060113 |
0.355 |
|
| 1993 |
Pyne SG, Boche G. Synthesis and conjugate and 1,2 addition reactions of a sterically hindered allylic sulfoximine Tetrahedron. 49: 8449-8464. DOI: 10.1016/S0040-4020(01)81928-1 |
0.407 |
|
| 1993 |
Boche G, Harms K, Marsch M. Structures of (ester) enolates and related compounds Macromolecular Symposia. 67: 97-110. DOI: 10.1002/Masy.19930670108 |
0.439 |
|
| 1993 |
Boche G, Marsch M, Harbach J, Harms K, Ledig B, Schubert F, Lohrenz JCW, Ahlbrecht H. [α‐(Dimethylamino)benzyllithium–Diethyl Ether]2, (S)‐α‐(Methylpivaloylamino)benzyllithium – (–)‐Sparteine, and [3‐Iodo‐2‐lithio‐1‐methylindole – 2 Tetrahydrofuran]2: Crystal Structure Investigations of α‐Lithiated Amines Chemische Berichte. 126: 1887-1894. DOI: 10.1002/Cber.19931260820 |
0.434 |
|
| 1993 |
Boche G, Bosold F, Lohrenz JCW, Opel A, Zulauf P. α‐Oxygen‐Substituted Organolithium Compounds and their Carbenoid Nature: Reactions with RLi and Other Nucleophiles, Experimental and IGLO‐Calculated 13C‐NMR Shifts of the Carbenoid C Atom Chemische Berichte. 126: 1873-1885. DOI: 10.1002/Cber.19931260819 |
0.408 |
|
| 1993 |
Boche G, Langlotz I, Marsch M, Harms K, Frenking G. [tert-Butylcyanide · Lithium Bis(trimethylsilyl)amide]2, a Model of the Intermediate RCN. MR′ Complex Formed in Reactions of Cyanides RCN with Organometallic Compounds R′M†‡ Angewandte Chemie. 32: 1171-1173. DOI: 10.1002/Anie.199311711 |
0.421 |
|
| 1993 |
Boche G, Marsch M, Müller A, Harms K. 1‐Chloro‐2,2‐bis(4‐chlorophenyl)‐1‐lithioethene · TMEDA · 2THF: Structure of a LiCl Carbenoid Angewandte Chemie. 32: 1032-1033. DOI: 10.1002/Anie.199310321 |
0.365 |
|
| 1993 |
Boche G, Langlotz I, Marsch M, Harms K, Frenking G. [tert‐Butylcyanid‐Lithiumbis(trimethylsilyl)amid]2, ein Modell des intermediären RCN · MR′‐Komplexes bei Reaktionen von Cyaniden RCN mit metallorganischen Verbindungen R'M Angewandte Chemie. 105: 1207-1209. DOI: 10.1002/Ange.19931050814 |
0.344 |
|
| 1993 |
Boche G, Marsch M, Müller A, Harms K. 1‐Chlor‐2,2‐bis(4‐chlorphenyl)‐1‐lithioethen · TMEDA· 2THF: Struktur eines Li‐CI‐Carbenoids Angewandte Chemie. 105: 1081-1082. DOI: 10.1002/Ange.19931050713 |
0.346 |
|
| 1992 |
Boche G, Fraenkel G, Cabral J, Harms K, Hommes NJRVE, Lohrenz J, Marsch M, Schleyer PvR. exo,exo-[1,3-Bis(trimethylsilyl)allyl]lithium-N,N,N',N'-tetramethylethylenediamine complex: crystal structure and dynamics in solution Journal of the American Chemical Society. 114: 1562-1565. DOI: 10.1021/Ja00031A004 |
0.423 |
|
| 1992 |
Boche G, Opel A, Marsch M, Harms K, Hallera F, Lohrenz JCW, Thümmler C, Koch W. α‐Oxygen‐Substituted Organolithium Compounds and Their Carbenoid Nature: Calculations of the Configurational Stability and of LiCH2OH Model Structures, Crystal Structure of Diphenyl(trimethylsilyloxy)methyllithium · 3 THF, and the Stereochemistry of the (Reverse) Brook Rearrangement Chemische Berichte. 125: 2265-2273. DOI: 10.1002/Cber.19921251015 |
0.428 |
|
| 1992 |
Hiller W, Frey S, Strähle J, Boche G, Zarges W, Harms K, Marsch M, Wollert R, Dehnicke K. Die Kristallstrukturen von {Li3(12-Krone-4)2[HC(CN)2]3}, {Na(15-Krone-5)-[HC(CN)2]} und {Na[N(nBu)4][HC(CN)2]2 · THF} Chemische Berichte. 125: 87-92. DOI: 10.1002/Cber.19921250114 |
0.379 |
|
| 1992 |
Boche G, Langlotz I, Marsch M, Harms K, Nudelman NES. [Lithium Piperidide–Piperidine]4: Crystal Structure of an Oligomeric 1:1 Lithium Amide–Amine Mixed Complex, an Intermediate in the N‐Lithiation of Amines Angewandte Chemie. 31: 1205-1207. DOI: 10.1002/Anie.199212051 |
0.388 |
|
| 1992 |
Boche G. Penetrated Ion Pairs: a New Form of Ion Pair Angewandte Chemie. 31: 731-732. DOI: 10.1002/Anie.199207311 |
0.333 |
|
| 1992 |
Boche G. Book Review: Preparative Polar Organometallic Chemistry 2. By L. Brandsma Angewandte Chemie. 31: 485-486. DOI: 10.1002/Anie.199204851 |
0.322 |
|
| 1992 |
Ledig B, Marsch M, Harms K, Boche G. Lithiodiphenylmethylisocyanide‐(—)‐sparteinebis(tetrahydrofuran):Crystal Structure of a Lithiated Isocyanide Angewandte Chemie. 31: 79-80. DOI: 10.1002/Anie.199200791 |
0.362 |
|
| 1992 |
Boche G, Langlotz I, Marsch M, Harms K, Nudelman NES. [Lithiumpiperidid‐Piperidin]4: Kristallstruktur eines oligomeren Lithiumamid‐Amin‐Komplexes, einer Zwischenstufe bei der Lithiierung von Aminen Angewandte Chemie. 104: 1239-1240. DOI: 10.1002/Ange.19921040922 |
0.356 |
|
| 1992 |
Boche G. Durchdrungene ionenpaare : ein neuer typ von Ionenpaaren Angewandte Chemie. 104: 742-743. DOI: 10.1002/Ange.19921040608 |
0.35 |
|
| 1992 |
Boche G. Preparative Polar Organometallic Chemistry 2. Von L. Brandsma. Springer, Berlin, 1990. XII, 227 S., Broschur DM 86.00. ‐ ISBN 3‐540‐52749‐4 Angewandte Chemie. 104: 251-251. DOI: 10.1002/Ange.19921040251 |
0.331 |
|
| 1992 |
Ledig B, Marsch M, Harms K, Boche G. Lithiodiphenylmethylisocyanid‐( — )‐Spartein‐Bis(tetrahydrofuran): Kristallstruktur eines lithiierten Isocyanids Angewandte Chemie. 104: 80-81. DOI: 10.1002/Ange.19921040124 |
0.37 |
|
| 1991 |
Meier C, Boche G. The modification of guanine nucleosides and nucleotides by the borderline arylamine carcinogens 4-methyl- and 4-methoxyaniline: Chemishy and structural characterization Carcinogenesis. 12: 1633-1640. PMID 1893521 DOI: 10.1093/Carcin/12.9.1633 |
0.56 |
|
| 1991 |
Zarges W, Marsch M, Harms K, Haller F, Frenking G, Boche G. [(C2H5O)2P(O)CHPhLi·N(CH2CH2)3N]∞: Festkörperstruktur, Aggregation in THF‐Lösung und Modellrechnungen zur Struktur eines Wadsworth‐Horner‐Emmons‐Reagenzes Chemische Berichte. 124: 861-866. DOI: 10.1002/Cber.19911240428 |
0.368 |
|
| 1991 |
Zarges W, Marsch M, Harms K, Frenking G, Boche G, Koch W. Röntgenstrukturuntersuchung von α‐(Trimethylsilyl)benzyllithium·Tetramethylendiamin [C6H5CH(SiMe3)Li·TMEDA] und α‐(Phenylthio)‐benzyllithium·3 Tetrahydrofuran [C6H5CH(SPh)Li·(THF)3] – zwei zentral‐chirale Benzyllithium‐Verbindungen Chemische Berichte. 124: 543-549. DOI: 10.1002/Cber.19911240321 |
0.429 |
|
| 1991 |
Bosold F, Zulauf P, Marsch M, Harms K, Lohrenz J, Boche G. [3‐Bromo‐2‐lithio‐1‐phenylsulfonylbenzofuran Diisopropyl Ether]2 and 3‐Fluoro‐2‐lithio‐1‐phenyl‐sulfonylbenzene · Pentamethyldiethylenetriamine : Crystal Structures of Compounds with Lithium and Halogen on Neighboring Carbon Atoms Angewandte Chemie. 30: 1455-1457. DOI: 10.1002/Anie.199114551 |
0.393 |
|
| 1991 |
Marsch M, Harms K, Zschage O, Hoppe D, Boche G. η1-(1S, 2E)-1-(N,N-diisopropylcarbamoyloxy)-3-trimethylsilylallyllithium()-Sparteine: Structure of a Chiral, Carbamoyloxy-substituted Allyllithium Compound Angewandte Chemie International Edition in English. 30: 321-323. DOI: 10.1002/Anie.199103211 |
0.411 |
|
| 1991 |
Bosold F, Zulauf P, Marsch M, Harms K, Lohrenz J, Boche G. [3‐Brom‐2‐lithiobenzofuran‐Diisopropylether]2 und 3‐Fluor‐2‐lithio‐1‐phenylsulfonylbenzol‐Pentamethyldiethylentriamin: Kristallstrukturen von Verbindungen mit Lithium und Halogen an benachbarten Kohlenstoffatomen Angewandte Chemie. 103: 1497-1499. DOI: 10.1002/Ange.19911031115 |
0.393 |
|
| 1991 |
Marsch M, Harms K, Zschage O, Hoppe D, Boche G. η1-(1S,2E)-1-(N, N-Diisopropylcarbamoyloxy)-3-trimethylsilyl-allyllithium-(-)-Spartein: Struktur einer chiralen, Carbamoyloxy-substituierten Allyllithium-Verbindung Angewandte Chemie. 103: 338-339. DOI: 10.1002/Ange.19911030327 |
0.363 |
|
| 1990 |
Meier C, Boche G. N-acetoxy-4-methoxyaniline, a model compound for the ultimate carcinogen of the phenacetin belated 4-ethoxyaniline Tetrahedron Letters. 31: 1693-1696. DOI: 10.1016/S0040-4039(00)88856-5 |
0.559 |
|
| 1990 |
Ulbrich R, Famulok M, Bosold F, Boche G. SN2 at nitrogen : the reaction of N-(4-cyanophenyl)-O-diphenylphosphinoylhydroxylamine with N-methylaniline. A model for the reactions of ultimate carcinogens of aromatic amines with (bio)nucleophiles Tetrahedron Letters. 31: 1689-1692. DOI: 10.1016/S0040-4039(00)88855-3 |
0.41 |
|
| 1990 |
Meier C, Boche G. N- (α-aminoacyloxy)-N-arylamines: Activation of aromatic amines to ultimate carcinogens by amino acids Tetrahedron Letters. 31: 1685-1688. DOI: 10.1016/S0040-4039(00)88854-1 |
0.564 |
|
| 1990 |
ULBRICH R, FAMULOK M, BOSOLD F, BOCHE G. ChemInform Abstract: SN2 at Nitrogen: The Reaction of N-(4-Cyanophenyl)-O-diphenylphosphinoylhydroxylamine with N-Methylaniline. A Model for the Reactions of Ultimate Carcinogens of Aromatic Amines with (Bio)Nucleophiles. Cheminform. 21. DOI: 10.1002/CHIN.199052364 |
0.568 |
|
| 1990 |
AHLBRECHT H, BOCHE G, HARMS K, MARSCH M, SOMMER H. ChemInform Abstract: Chiral Homoenolate Equivalents. Part 4. Crystal Structure of a Chiral 1-Aminoallyllithium Compound: Dimeric, Intramolecularly Chelated (3S)-3-Lithio-1-((S)-2-(methoxymethyl)pyrrolidino)-1,3-diphenylpropene Cheminform. 21. DOI: 10.1002/CHIN.199046055 |
0.287 |
|
| 1990 |
MEIER C, BOCHE G. ChemInform Abstract: 1H and 13C NMR Conformational Analysis and Minimal-Potential-Energy Calculations with Deoxyguanosine, Guanosine and 5′-Guanosinemonophosphate Adducts of the Borderline Carcinogen 4-Methylaniline. Cheminform. 21. DOI: 10.1002/CHIN.199045313 |
0.496 |
|
| 1990 |
MEIER C, BOCHE G. ChemInform Abstract: N-Aryl-O-(α-aminoacyl)hydroxylamines: Model Reactions with Deoxyguanosine, Guanosine and 5′-Guanosinemonophosphate for the Activation of Monocyclic Aromatic Amines (e.g. Phenacetin) into Ultimate Carcinogens. Cheminform. 21. DOI: 10.1002/CHIN.199044275 |
0.547 |
|
| 1990 |
MEIER C, BOCHE G. ChemInform Abstract: N-Aryl-O-(α-aminoacyl)hydroxylamines: Model Reactions for the Activation of Monocyclic Aromatic Amines into Ultimate Carcinogens with α-Amino Acids. Cheminform. 21. DOI: 10.1002/CHIN.199044274 |
0.533 |
|
| 1990 |
MARSCH M, HARMS K, LOCHMANN L, BOCHE G. ChemInform Abstract: (nBuLi·LiOtBu)4, Structure of an n-Butyllithium-Lithium-tert.-butoxide Complex in a Single Crystal Cheminform. 21. DOI: 10.1002/CHIN.199019054 |
0.304 |
|
| 1990 |
BOSOLD F, BOCHE G. ChemInform Abstract: The Ultimate Carcinogen, O-Acetyl-N-(2-fluorenyl)hydroxylamine (“N-Acetoxy-2-aminofluorene”) and Its in vitro Reaction to form 2-(N-(Deoxyguanosin-8-yl)amino)fluorene. Cheminform. 21. DOI: 10.1002/CHIN.199014345 |
0.317 |
|
| 1990 |
Ahlbrecht H, Boche G, Harms K, Marsch M, Sommer H. Chirale Homoenolat-Äquivalente, IV. Kristallstruktur einer chiralen 1-Aminoallyllithium-Verbindung: dimeres, intramolekular chelatisiertes (3S)-3-Lithio-1-[(S)-2-(methoxymethyl)pyrrolidino]-1,3-diphenylpropen Chemische Berichte. 123: 1853-1858. DOI: 10.1002/Cber.19901230917 |
0.406 |
|
| 1990 |
Meier C, Boche G. 1H- und 13C-NMR-Konformationsanalysen und Minimal-Potential-Energie-Rechnungen an Desoxyguanosin-, Guanosin- und 5′-Guanosinmonophosphat-Addukten des Grenzcarcinogens 4-Methylanilin Chemische Berichte. 123: 1707-1713. DOI: 10.1002/Cber.19901230821 |
0.569 |
|
| 1990 |
Meier C, Boche G. N‐Aryl‐O‐(α‐aminoacyl)hydroxylamine: Modellreaktionen mit Desoxyguanosin, Guanosin und 5′‐Guanosinmonophosphat zur Aktivierung monocyclischer aromatischer Amine (z. B. Phenacetin) zu ultimaten Carcinogenen Chemische Berichte. 123: 1699-1705. DOI: 10.1002/Cber.19901230820 |
0.602 |
|
| 1990 |
Meier C, Boche G. N‐Aryl‐O‐(α‐aminoacyl)hydroxylamine: Modellreaktionen zur Aktivierung von monocyclischen aromatischen Aminen zu ultimaten Carcinogenen durch α‐Aminosäuren Chemische Berichte. 123: 1691-1698. DOI: 10.1002/Cber.19901230819 |
0.572 |
|
| 1990 |
Boche G. Book Review: Preparative Polar Organometallic Chemistry. Vol. 1. By L. Brandsma and H. D. Verkruijsse Angewandte Chemie. 29: 562-562. DOI: 10.1002/Anie.199005621 |
0.329 |
|
| 1990 |
Marsch M, Harms K, Lochmann L, Boche G. [nBuLi · LiOtBu]4, Solid‐State Structure of an n‐Butyllithium–Lithium tert‐Butoxide Complex Angewandte Chemie. 29: 308-309. DOI: 10.1002/Anie.199003081 |
0.35 |
|
| 1990 |
Bosold F, Boche G. The Ultimate Carcinogen, O‐Acetyl‐N‐(2‐fluorenyl)hydroxylamine (“N‐Acetoxy‐2‐aminofluorene”), and Its Reaction in vitro to Form 2‐[N‐(Deoxyguanosin‐8‐yl)amino] fluorene Angewandte Chemie. 29: 63-64. DOI: 10.1002/Anie.199000631 |
0.376 |
|
| 1990 |
Marsch M, Harms K, Lochmann L, Boche G. [nBuLi·LiOtBu]4, Struktur eines n‐Butyllithium‐Lithium‐tert‐butoxid‐Komplexes im Kristall Angewandte Chemie. 102: 334-336. DOI: 10.1002/Ange.19901020333 |
0.345 |
|
| 1990 |
Bosold F, Boche G. Das ultimate Carcinogen O-Acetyl-N-(2-fluorenyl)-hydroxylamin (N-Acetoxy-2-aminofluoren) und seine in-vitro-Reaktion zu 2-[N-(Desoxyguanosin-8-yl)amino]fluoren Angewandte Chemie. 102: 99-100. DOI: 10.1002/Ange.19901020131 |
0.382 |
|
| 1989 |
Pyne SG, Boche G. Chiral sulfur compounds. 7. Stereoselective reactions of lithium and zinc tert-butyl phenylmethyl sulfoxide with carbonyl compounds and imines Journal of Organic Chemistry. 54: 2663-2667. DOI: 10.1021/Jo00272A040 |
0.408 |
|
| 1989 |
Famulok M, Bosold F, Boche G. Synthesis of N-acetoxy-2-aminonaphthaline, an ultimate carcinogen of the carcinogenic 2-naphthylamine, and its reactions with (bio)nucleophiles Tetrahedron Letters. 30: 321-324. DOI: 10.1016/S0040-4039(00)95190-6 |
0.393 |
|
| 1989 |
Kneuper H, Harms K, Boche G. FunktionalisierteÜbergangsmetallalkyle: Synthese und Kristallstruktur von Ph3PAuCHPhSO2-t-Bu Journal of Organometallic Chemistry. 364: 275-279. DOI: 10.1016/0022-328X(89)85350-1 |
0.397 |
|
| 1989 |
ZARGES W, MARSCH M, HARMS K, BOCHE G. ChemInform Abstract: ((Li2(Me3SiCCN))12(Et2O)6(C6H14)), Crystal Structure with the Trimethylsilylacetonitrile Dianion. Cheminform. 20. DOI: 10.1002/CHIN.198939231 |
0.277 |
|
| 1989 |
KNEUPER H, ZIMMERMANN C, HARMS K, BOCHE G. ChemInform Abstract: Functionalized Transition Metal Alkyls. Part 2. Synthesis, Crystal Structure, and Reactivity of (η5-C5H5)W(CO)3-CH2-S(O)-C6H5, an α-Metallated Sulfoxide. Cheminform. 20. DOI: 10.1002/CHIN.198935299 |
0.27 |
|
| 1989 |
FAMULOK M, BOSOLD F, BOCHE G. ChemInform Abstract: Synthesis of N-Acetoxy-2-aminonaphthalene, an Ultimate Carcinogen of the Carcinogenic 2-Naphtylamine, and Its in vitro Reactions with (Bio)-Nucleophiles. Cheminform. 20. DOI: 10.1002/CHIN.198930310 |
0.565 |
|
| 1989 |
FAMULOK M, BOCHE G. ChemInform Abstract: N-(Deoxyguanosin-8-yl)aniline from the in-vitro Reaction of N-Acetoxyaniline with Deoxyguanosine and DNA. Cheminform. 20. DOI: 10.1002/CHIN.198930307 |
0.287 |
|
| 1989 |
FAMULOK M, BOSOLD F, BOCHE G. ChemInform Abstract: Synthesis of O-Acetyl-N-(4-biphenylyl)hydroxylamine, a Decisive Metabolite of the Carcinogenic 4-Aminobiphenyl, and Its Reaction with Deoxyguanosine. Cheminform. 20. DOI: 10.1002/CHIN.198923145 |
0.299 |
|
| 1989 |
BOCHE G, HARMS K, MARSCH M. ChemInform Abstract: X-Ray Structure Determination of (1-Cyano-2,2-dimethylcyclopropyllithium·Tetrahydrofuran)∞: A Tetrahedral Anionic α-Cyano Carbon Atom. Cheminform. 20. DOI: 10.1002/CHIN.198902050 |
0.273 |
|
| 1989 |
Zarges W, Marsch M, Harms K, Boche G. η1-C6H5CH2Li•THF•TMEDA, Kristallstruktur eines Benzyllithium•THF•TMEDA-Komplexes mit einem pyramidalen Benzyl-C-Atom Chemische Berichte. 122: 2303-2309. DOI: 10.1002/Cber.19891221217 |
0.407 |
|
| 1989 |
Zarges W, Marsch M, Harms K, Boche G. [{Li2(Me3SiCCN)}12(Et2O)6(C6H14)], Kristallstruktur mit dem Trimethylsilylacetonitril‐Dianion Chemische Berichte. 122: 1307-1311. DOI: 10.1002/Cber.19891220714 |
0.411 |
|
| 1989 |
Kneuper H, Zimmermann C, Harms K, Boche G. Funktionalisierte Übergangsmetallalkyle, II. Synthese, Kristallstruktur und Reaktivität von (η5‐C5H5)W(CO)3 CH2S(O)C6H5, einem α‐metallierten Sulfoxid Chemische Berichte. 122: 1043-1047. DOI: 10.1002/Cber.19891220605 |
0.375 |
|
| 1989 |
Zarges W, Marsch M, Harms K, Boche G. X‐Ray Structure Analysis of α‐Lithiophenylacetonitrile · Lithium Diisopropyl amide· 2 Tetramethylethylenediamine—a “Quasi‐Dianion Complex” Angewandte Chemie. 28: 1392-1394. DOI: 10.1002/Anie.198913921 |
0.372 |
|
| 1989 |
Boche G. Book Review: Chemical Carcinogens. Activation Mechanisms, Structural and Electronic Factors, and Reactivity. Bioactive Molecules Series, Vol. 5. Edited by P. Politzer and F. J. Martin, Jr. Angewandte Chemie. 28: 932-932. DOI: 10.1002/Anie.198909321 |
0.337 |
|
| 1989 |
Famulok M, Boche G. Formation of N‐(Deoxyguanosin‐8‐yl)aniline in the in vitro Reaction of N‐Acetoxyaniline with Deoxyguanosine and DNA Angewandte Chemie. 28: 468-469. DOI: 10.1002/Anie.198904681 |
0.351 |
|
| 1989 |
Famulok M, Bosold F, Boche G. Synthesis of O‐Acetyl‐N (4‐biphenylyl)hydroxylamine (“NAcetoxy‐4‐aminobiphenyl”), an Ultimate Metabolite of Carcinogenic 4‐Aminobiphenyl, and Its Reaction with Deoxyguanosine Angewandte Chemie. 28: 337-338. DOI: 10.1002/Anie.198903371 |
0.377 |
|
| 1989 |
Boche G. The Structure of Lithium Compounds of Sulfones, Sulfoximides, Sulfoxides, Thioethers and 1,3-Dithianes, Nitriles, Nitro Compounds and Hydrazones Angewandte Chemie. 28: 277-297. DOI: 10.1002/Anie.198902771 |
0.406 |
|
| 1989 |
Buchholz S, Harms K, Massa W, Boche G. Hydrogen Bonds between an NH 4⊕ Ion and a Carbanion—Crystal Structure of Ammonium 1,2,4‐Tricyanocyclopentadienide Angewandte Chemie. 28: 73-75. DOI: 10.1002/Anie.198900731 |
0.364 |
|
| 1989 |
Buchholz S, Harms K, Marsch M, Massa W, Boche G. Model of a Solvent‐Shared Ion Pair with NH ⃛C Hydrogen Bonds between Amine and Carbanion—Crystal Structure of [Fluorenyllithium·2 Ethylenediamine]∞ Angewandte Chemie. 28: 72-73. DOI: 10.1002/Anie.198900721 |
0.371 |
|
| 1989 |
Boche G. Preparative Polar Organometallic Chemistry. Vol. 1. Von L. Brandsma und H. D. Verkruijsse. Springer, Berlin 1987. 240 S., kartoniert, DM 78.00. – ISBN 3‐540‐16916‐4 Angewandte Chemie. 101: 1567-1567. DOI: 10.1002/Ange.19891011130 |
0.343 |
|
| 1989 |
Zarges W, Marsch M, Harms K, Boche G. Röntgenstrukturanalyse von α‐Lithiophenylacetonitril · Lithiumdiisopropylamid · 2 Tetramethyl‐ethylendiamin – ein „Quasi‐Dianion‐Komplex”︁ Angewandte Chemie. 101: 1424-1425. DOI: 10.1002/Ange.19891011033 |
0.34 |
|
| 1989 |
Famulok M, Boche G. N‐(Desoxyguanosin‐8‐yl)anilin aus der in‐vitro‐Umsetzung von N‐Acetoxyanilin mit Desoxyguanosin und DNA Angewandte Chemie. 101: 470-471. DOI: 10.1002/Ange.19891010413 |
0.314 |
|
| 1989 |
Famulok M, Bosold F, Boche G. Synthese von O-Acetyl-N-(4-biphenylyl)hydroxylamin („N-Acetoxy-4-aminobiphenyl”), einem entscheidenden Metaboliten des carcinogenen 4-Aminobiphenyls, und seine Reaktion mit Desoxyguanosin† Angewandte Chemie. 101: 349-350. DOI: 10.1002/Ange.19891010326 |
0.401 |
|
| 1989 |
Boche G. Zur Struktur der Lithiumverbindungen von Sulfonen, Sulfoximiden, Sulfoxiden, Thioethern und 1,3‐Dithianen, Nitrilen, Nitroverbindungen und Hydrazonen Angewandte Chemie. 101: 286-306. DOI: 10.1002/Ange.19891010306 |
0.38 |
|
| 1989 |
Buchholz S, Harms K, Massa W, Boche G. Wasserstoffbrücken zwischen einem NH 4⊕‐Ion und einem Carbanion – Kristallstruktur von Ammonium‐1,2,4‐tricyancyclopentadienid Angewandte Chemie. 101: 58-59. DOI: 10.1002/Ange.19891010110 |
0.37 |
|
| 1989 |
Buchholz S, Harms K, Marsch M, Massa W, Boche G. Modell eines solvens‐verbrückten Ionenpaares mit NH ⃛C‐Wasserstoffbrücken zwischen Amin und Carbanion – Kristallstruktur von [Fluorenyllithium·2Ethylendiamin]∞ Angewandte Chemie. 101: 57-58. DOI: 10.1002/Ange.19891010109 |
0.372 |
|
| 1988 |
Boche G, Harms K, Marsch M. X-ray structure determination of [1-cyano-2,.2-dimtheylcyclopropyllithium.cntdot.tetrahydrofuran].infin.: a tetrahedral anionic .alpha.-cyano carbon atom Journal of the American Chemical Society. 110: 6925-6926. DOI: 10.1021/Ja00228A073 |
0.348 |
|
| 1988 |
Bosold F, Boche G, Kleemiβ W. Formation of acceptor substituted phenylnitrenes via α-elimination under mild conditions Tetrahedron Letters. 29: 1781-1783. DOI: 10.1016/S0040-4039(00)82042-0 |
0.399 |
|
| 1988 |
Boche G, Meier C, Kleemiβ W. Hydrazines and azo compounds from O-diphenylphosphinoyl arylhydroxylamines Tetrahedron Letters. 29: 1777-1779. DOI: 10.1016/S0040-4039(00)82041-9 |
0.575 |
|
| 1988 |
Boche G. Rearrangements of “Carbanions” Topics in Current Chemistry. 146: 1-56. DOI: 10.1007/Bfb0111254 |
0.36 |
|
| 1988 |
HOLLSTEIN W, HARMS K, MARSCH M, BOCHE G. ChemInform Abstract: X-Ray Structure Analysis of the Li2 Compound of Bis(trimethylsilyl)methyl Phenyl Sulfone; Structural Units of an α-Sulfonyl and a Complexed-Stabilized ortho-Sulfonyl “Carbanion” Cheminform. 19. DOI: 10.1002/CHIN.198810070 |
0.313 |
|
| 1988 |
Enders D, Bachstädter G, Kremer KAM, Marsch M, Harms K, Boche G. Structure of a Chiral Lithium Azaenolate: Monomeric, Intramolecular Chelated Lithio-2-acetylnaphthalene-SAMP-hydrazone Angewandte Chemie International Edition in English. 27: 1522-1524. DOI: 10.1002/Anie.198815221 |
0.391 |
|
| 1988 |
Boche G, Bosold F, Schröder S. N-Aryl-O-acylhydroxylamines: Preparation by O-Acylation or N → O Transacylation and Reaction with Amines; Model Reactions for Key Steps Connected with the Carcinogenicity of Aromatic Amines† Angewandte Chemie. 27: 973-974. DOI: 10.1002/Anie.198809731 |
0.404 |
|
| 1988 |
Hollstein W, Harms K, Marsch M, Boche G. X‐Ray Structure Investigation of 2,2‐Diphenyl‐1‐(phenylsulfonyl)cyclopropyllithium–Dimethoxyethane (2/3): A Sulfonyl “Carbanion” Having an α‐C Atom with a Tetrahedral Configuration Angewandte Chemie. 27: 846-847. DOI: 10.1002/Anie.198808461 |
0.347 |
|
| 1988 |
Enders D, Bachstädter G, Kremer KAM, Marsch M, Harms K, Boche G. Struktur eines chiralen Lithium‐azaenolats: monomeres, intramolekular chelatisiertes Lithio‐2‐acetylnaphthalin‐SAMP‐hydrazon Angewandte Chemie. 100: 1580-1581. DOI: 10.1002/Ange.19881001117 |
0.371 |
|
| 1988 |
Boche G, Bosold F, Schröder S. N‐Aryl‐O‐acylhydroxylamine: Herstellung durch O‐Acylierung oder N→O‐Umacylierung und Umsetzung mit Aminen; Modellreaktionen für Schlüsselschritte im Zusammenhang mit der Carcinogenität aromatischer Amine Angewandte Chemie. 100: 965-966. DOI: 10.1002/Ange.19881000716 |
0.393 |
|
| 1988 |
Hollstein W, Harms K, Marsch M, Boche G. Röntgenstrukturuntersuchung von 2,2‐Diphenyl‐1‐(phenylsulfonyl)cyclopropyllithium‐Dimethoxyethan(2/3): ein Sulfonyl‐„Carbanion”︁ mit tetraedrisch konfiguriertem α‐C‐Atom Angewandte Chemie. 100: 868-869. DOI: 10.1002/Ange.19881000616 |
0.358 |
|
| 1987 |
MARSCH M, HARMS K, MASSA W, BOCHE G. ChemInform Abstract: Crystal Structure of the η1-Allyl-Grignard Compound Bis-(allylmagnesium chloride-TMEDA) (I) (TMEDA = Tetramethylethylenediamine) Cheminform. 18. DOI: 10.1002/CHIN.198742061 |
0.323 |
|
| 1987 |
KLEBE G, BOEHN KH, MARSCH M, BOCHE G. ChemInform Abstract: Crystal Structure of (α-Nitrobenzyllithium·Ethanol)n; a Lithiumnitronate-Ethanol Interaction Cheminform. 18. DOI: 10.1002/CHIN.198718050 |
0.28 |
|
| 1987 |
MARSCH M, MASSA W, HARMS K, BAUM G, BOCHE G. ChemInform Abstract: (α-(Phenylsulfinyl)-α-methylbenzyllithium-tetramethylethylenediamin# e)2: Crystal Structure of an α-Sulfinyl “Carbanion”. Cheminform. 18. DOI: 10.1002/CHIN.198712072 |
0.265 |
|
| 1987 |
Hollstein W, Harms K, Marsch M, Boche G. X‐Ray Structure Analysis of the Li2‐Compound of Bis(trimethylsilyl)metnyl Phenyl Sulfone; Structural Units of an α‐Sulfonyl‐ and a Complex‐Stabilized ortho‐Sulfonyl‐“Carbanion” Angewandte Chemie. 26: 1287-1288. DOI: 10.1002/Anie.198712871 |
0.378 |
|
| 1987 |
Marsch M, Harms K, Massa W, Boche G. Crystal Structure of the η1‐Allyl‐Grignard Compound Bis(allylmagnesium chloride‐TMEDA) Angewandte Chemie. 26: 696-697. DOI: 10.1002/Anie.198706961 |
0.387 |
|
| 1987 |
Klebe G, Böhn KH, Marsch M, Boche G. Crystal Structure of [α‐Nitrobenzyllithium · Ethanol]n; A Lithium Nitronate‐Ethanol Interaction Angewandte Chemie. 26: 78-79. DOI: 10.1002/Anie.198700781 |
0.369 |
|
| 1987 |
Hollstein W, Harms K, Marsch M, Boche G. Röntgenstrukturanalyse der Li2‐Verbindung von Bis(trimethylsilyl)methylphenylsulfon; Strukturelemente eines α‐Sulfonyl‐ und eines komplexstabilisierten ortho ‐Sulfonyl‐ „Carbanions”︁ Angewandte Chemie. 99: 1279-1280. DOI: 10.1002/Ange.19870991209 |
0.414 |
|
| 1987 |
Marsch M, Harms K, Massa W, Boche G. Kristallstruktur der η1‐Allyl‐Grignard‐Verbindung Bis(allylmagnesiumchlorid‐TMEDA) Angewandte Chemie. 99: 706-707. DOI: 10.1002/Ange.19870990727 |
0.383 |
|
| 1987 |
Klebe G, Böhn KH, Marsch M, Boche G. Kristallstruktur von [α‐Nitrobenzyllithium · Ethanol]n; eine Lithiumnitronat‐Ethanol‐Wechselwirkung Angewandte Chemie. 99: 62-64. DOI: 10.1002/Ange.19870990111 |
0.335 |
|
| 1986 |
Boche G, Sommerlade RH. Oxidation of amines with bis-(diphenylphosphinyl)peroxide to give o-phosphinylated aminating reagents Tetrahedron. 42: 2703-2706. DOI: 10.1016/S0040-4020(01)90556-3 |
0.381 |
|
| 1986 |
Boche G, Sommerlade RH, Bosold F. N-Aryl-O-(diphenylphosphinoyl)hydroxylamines: Electrophilic Amination of Amines to Hydrazines. Cheminform. 17. DOI: 10.1002/Chin.198641268 |
0.397 |
|
| 1986 |
Boche G, Marsch M, Harms K. [(α-Cyanobenzyllithium·Tetramethylethylenediamine)2·Benzene]: X-Ray Structure Analysis of an α-Nitrile "Carbanion" Cheminform. 17. DOI: 10.1002/Chin.198630051 |
0.354 |
|
| 1986 |
Boche G, Etzrodt H, Marsch M, Massa W, Baum G, Dietrich H, Mahdi W. Crystal Structure of the η3‐Allyllithium Compound [1,3‐Diphenylallyllithium‐Diethyl Ether] Cheminform. 17. DOI: 10.1002/Chin.198618078 |
0.387 |
|
| 1986 |
Boche G, Etzrodt H, Massa W, Baum G. Polymorphism at an Organolithium Compound: Dilithium-1,2-diphenylbenzocyclobutadien-diid-2 Tetramethylethylendiamine. Cheminform. 17. DOI: 10.1002/Chin.198603051 |
0.342 |
|
| 1986 |
Marsch M, Massa W, Baum G, Boche G, Harms K. [α‐(Phenylsulfinyl)‐α‐methylbenzyllithium‐tetramethylethylenediamine]2: Crystal Structure of an α‐Sulfinyl “Carbanion” Angewandte Chemie. 25: 1011-1012. DOI: 10.1002/Anie.198610111 |
0.356 |
|
| 1986 |
Boche G, Sommerlade RH, Bosold F. N-Aryl-O-(diphenylphosphinoyl)hydroxylamines: Electrophilic Amination of Amines to Hydrazines; a Model Reaction for the Carcinogenicity of Aromatic Amines† Angewandte Chemie. 25: 562-563. DOI: 10.1002/Anie.198605621 |
0.419 |
|
| 1986 |
Boche G, Marsch M, Harms K. [(α‐Cyanobenzyllithium. Tetramethylethylenediamine)2. Benzene]: X‐ray Structure Analysis of an α‐Nitrile “Carbanion” Angewandte Chemie. 25: 373-374. DOI: 10.1002/Anie.198603731 |
0.361 |
|
| 1986 |
Boche G, Etzrodt H, Marsch M, Massa W, Baum G, Dietrich H, Mahdi W. Crystal Structure of the η3‐Allyllithium Compound [1,3‐Diphenylallyllithium · Diethyl Ether]n Angewandte Chemie. 25: 104-105. DOI: 10.1002/Anie.198601041 |
0.413 |
|
| 1986 |
Marsch M, Massa W, Harms K, Baum G, Boche G. [α‐(Phenylsulfinyl)‐α‐methylbenzyllithium‐Tetramethylethylendiamin]2: Kristallstruktur eines α‐Sulfinyl‐„Carbanions”︁ Angewandte Chemie. 98: 1004-1005. DOI: 10.1002/Ange.19860981114 |
0.356 |
|
| 1986 |
Boche G, Sommerlade RH, Bosold F. N‐Aryl‐O‐(diphenylphosphinoyl)hydroxylamine: Elektrophile Aminierung von Aminen zu Hydrazinen; zur Cancerogenität aromatischer Amine Angewandte Chemie. 98: 563-564. DOI: 10.1002/Ange.19860980620 |
0.375 |
|
| 1986 |
Boche G, Marsch M, Harms K. [(a‐Cyanbenzyllithium·Tetramethylethylendiamin)2·Benzol]: Röntgen‐Strukturanalyse eines α‐Nitril‐„Carbanions”︁ Angewandte Chemie. 98: 373-374. DOI: 10.1002/Ange.19860980434 |
0.356 |
|
| 1986 |
Boche G, Etzrodt H, Marsch M, Massa W, Baum G, Dietrich H, Mahdi W. Kristallstruktur der η3-Allyllithium-Verbindung [1,3-Diphenylallyllithium Diethylether]n† Angewandte Chemie. 98: 84-85. DOI: 10.1002/Ange.19860980112 |
0.367 |
|
| 1985 |
Boche G, Eiben R. Preparation of some 2,4,6-cycloheptatriene-1-yl ketones. Strong preference for the norcaradiene isomer in the case of the 2,4,6-cycloheptatriene-1-yl t-butyl ketone Tetrahedron Letters. 26: 1289-1292. DOI: 10.1016/S0040-4039(00)94872-X |
0.257 |
|
| 1985 |
BOCHE G, MARSCH M, HARMS K, SHELDRICK GM. ChemInform Abstract: Röntgen-Strukturuntersuchung von [α-(Phenylsulfonyl(benzyllithium-Tetramethyl-ethylendiamin]2Chiralität eines α-Sulfonyl-"Carbanions" Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198545048 |
0.35 |
|
| 1985 |
BOCHE G, EIBEN R. ChemInform Abstract: PREPARATION OF SOME 2,4,6-CYCLOHEPTATRIENE-1-YL KETONES. STRONG PREFERENCE FOR THE NORCARADIENE ISOMER IN THE CASE OF THE 2,4,6-CYCLOHEPTATRIENE-1-YL TERT-BUTYL KETONE Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198526160 |
0.299 |
|
| 1985 |
Boche G, Bosold F, Eiben R. EASY ROTATION AROUND THE CARBON-CARBON BOND IN LITHIUM α-AMINOENOLATES: A COMPARISON Cheminform. 16. DOI: 10.1002/Chin.198513045 |
0.349 |
|
| 1985 |
Boche G, Etzrodt H, Massa W, Baum G. Polymorphism of an Organolithium Compound: Dilithium 1,2‐diphenylbenzocyclobutadienediide · 2 Tetramethylethylenediamine Angewandte Chemie. 24: 863-864. DOI: 10.1002/Anie.198508631 |
0.351 |
|
| 1985 |
Boche G, Marsch M, Harms K, Sheldrick GM. X-Ray Structure Determination of [?-(Phenylsulfonyl)benzyllithium-Tetramethylethylenediamine]2: Chirality of an ?-Sulfonyl ?Carbanion? Angewandte Chemie International Edition in English. 24: 573-575. DOI: 10.1002/Anie.198505731 |
0.344 |
|
| 1985 |
Boche G, Etzrodt H, Massa W, Baum G. Polymorphie bei einer Organolithium-Verbindung: Dilithium-1,2-diphenyl-benzocyclobutadien-diid· 2 Tetramethylendiamin†‡ Angewandte Chemie. 97: 858-859. DOI: 10.1002/Ange.19850971012 |
0.398 |
|
| 1985 |
Boche G, Marsch M, Harms K, Sheldrick GM. Röntgen-Strukturuntersuchung von [α-(Phenylsulfonyl)benzyllithium-Tetramethylethylendiamin]2: Chiralität eines α-Sulfonyl- „Carbanions” Angewandte Chemie. 97: 577-578. DOI: 10.1002/Ange.19850970714 |
0.375 |
|
| 1984 |
Dietrich H, Mahdi W, Schleyer PvR, Neugebauer W, Clark T, Wilhelm D, Boche G, Etzrodt H. New lithium organic structures and their interpretation Acta Crystallographica Section A. 40. DOI: 10.1107/S0108767384091315 |
0.347 |
|
| 1984 |
Boche G, Wagner H. Nitrenoids LiRN–OR1 in electrophilic amination reactions of organolithium compounds. A theoretical study Journal of the Chemical Society, Chemical Communications. 1591-1592. DOI: 10.1039/C39840001591 |
0.42 |
|
| 1984 |
Schleyer PvR, Kos AJ, Wilhelm D, Clark T, Boche G, Decher G, Etzrodt H, Dietrich H, Mahdi W. The influence of carbanion orbital orientation and charge distribution on the structures of polylithium compounds Journal of the Chemical Society, Chemical Communications. 1495-1496. DOI: 10.1039/C39840001495 |
0.358 |
|
| 1984 |
Boche G, Decher G, Etzrodt H, Dietrich H, Mahdi W, Kos AJ, Schleyer PvR. X-Ray crystal structure of [{o-C6H4(CHPh)2}{Li(tmeda)}2](tmedaMe2NCH2CH2NMe2). Unsymmetrical lithium bridging and (E,E)-conformation of the phenyl groups Journal of the Chemical Society, Chemical Communications. 1493-1494. DOI: 10.1039/C39840001493 |
0.401 |
|
| 1984 |
Boche G, Schneider DR, Wernicke K. Electron transfer on cis- and trans-1,2-diphenylcyclopropane: stereoisomerization and formation of 1,3-diphenylpropene and 1,3-diphenylpropane Tetrahedron Letters. 25: 2961-2964. DOI: 10.1016/S0040-4039(01)81337-X |
0.382 |
|
| 1984 |
Boche G, Bigalke J. Trimethylsilyl ethyl orthopropiolate - preparation and use as a propiolate anion equivalent Tetrahedron Letters. 25: 955-958. DOI: 10.1016/S0040-4039(01)80072-1 |
0.356 |
|
| 1984 |
Ahlbrecht H, Zimmermann K, Boche G, Decher G. The geometry of allyl-alkali-metal compounds. A 13C NMR reinvestigation Journal of Organometallic Chemistry. 262: 1-10. DOI: 10.1016/S0022-328X(00)99116-2 |
0.39 |
|
| 1984 |
Stahl K, Boche G, Massa W. 1,1′-Bis(N,N-dimethylamino)ferrocene,1,1′-bis(N,N-dimethylamino) cobaltocenium hexafluorophosphate and 1,1′-bis(N,N-dimethylamino)titanocene dichloride. Crystal structure of 1,1′-bis(N,N-dimethylamino)titanocene dichloride Journal of Organometallic Chemistry. 277: 113-125. DOI: 10.1016/0022-328X(84)80686-5 |
0.416 |
|
| 1984 |
Boche G, Bosold F, Eiben R. Easy Rotation about the Exocylic Carbon-Carbon Bond in Lithium α-Aminoenolates: A Comparison† Angewandte Chemie. 23: 797-798. DOI: 10.1002/Anie.198407971 |
0.348 |
|
| 1984 |
Boche G. Book Review: Isotopeneffekte bei chemischen Reaktionen. By Alfred V. Willi Angewandte Chemie. 23: 537-538. DOI: 10.1002/Anie.198405372 |
0.287 |
|
| 1984 |
Boche G, Bosold F, Eiben R. Leichte Rotation um die exocyclische Kohlenstoff‐Kohlenstoffbindung in Lithium‐α‐aminoenolaten: ein Vergleich Angewandte Chemie. 96: 788-789. DOI: 10.1002/Ange.19840961011 |
0.296 |
|
| 1984 |
Boche G. Isotopeneffekte bei chemischen Reaktionen. Von Alfred V. Willi. Georg Thieme Verlag, Stuttgart 1983. X, 180 S., geb. DM 80.00 Angewandte Chemie. 96: 627-627. DOI: 10.1002/Ange.19840960840 |
0.318 |
|
| 1983 |
Boche G, Etzrodt H. The reaction of n-butyllithium/sodium(potassium) tert.-butoxide (Lochmann-Schlosser base) with a ch-acid leads to organo-sodium(potassium) compounds. An NMR spectroscopical study of several organo-lithium, -sodium and -potassium compounds in tetrahydrofuran-D8 Tetrahedron Letters. 24: 5477-5480. DOI: 10.1016/S0040-4039(00)94116-9 |
0.389 |
|
| 1983 |
Boche G, Marsch M. Ring opening in the reaction of diphenylcyclopropane derivatives with strong base: evidence for a proton transfer and against an electron transfer reaction. Facile disrotatory ring opening of a cyclopropyl anion at -75°C Tetrahedron Letters. 24: 3225-3228. DOI: 10.1016/S0040-4039(00)88141-1 |
0.404 |
|
| 1983 |
Decher G, Boche G. The positions of the hydrogen atoms in allyllithium and solvated allyllithium species. A MNDO study Journal of Organometallic Chemistry. 259: 31-36. DOI: 10.1016/0022-328X(83)85154-7 |
0.362 |
|
| 1983 |
Wagner H, Boche G. Nitrocyclopropyl‐Anion: A Triplet Ground State Molecule?? Helvetica Chimica Acta. 66: 842-844. DOI: 10.1002/Hlca.19830660317 |
0.376 |
|
| 1983 |
Wagner H‐, Boche G. Nitrocyclopropyl Anion: A Triplet Ground State Molecule? Cheminform. 14. DOI: 10.1002/Chin.198331072 |
0.315 |
|
| 1983 |
Boche G, Bernheim M, Niessner M. 1-Alkynylamines By Electrophilic Amination Cheminform. 14. DOI: 10.1002/Chin.198315175 |
0.396 |
|
| 1983 |
Wilhelm D, Clark T, Schleyer PvR, Buckl K, Boche G. Notizen: Das Tribenzylidenmethan‐Dianion Chemische Berichte. 116: 1669-1673. DOI: 10.1002/Cber.19831160441 |
0.38 |
|
| 1983 |
Boche G, Bernheim M, Niessner M. 1‐Alkynylamines by Electrophilic Amination Angewandte Chemie. 22: 53-54. DOI: 10.1002/Anie.198300532 |
0.323 |
|
| 1983 |
Boche G, Bernheim M, Nießner M. 1‐Alkinylamine durch elektrophile Aminierung Angewandte Chemie. 95: 48-48. DOI: 10.1002/Ange.19830950109 |
0.318 |
|
| 1982 |
Boche G, Bosold F, NieBner M. Electrophilic amination of acyl anion equivalents: mild oxidation of aldehydes to amides via 0-(trimethylsilyl)aldehyde cyanohydrin anions Tetrahedron Letters. 23: 3255-3256. DOI: 10.1016/S0040-4039(00)87584-X |
0.41 |
|
| 1982 |
Boche G, Schrott W. A chiral reagent inducing asymmetry in electrophilic amination reactions Tetrahedron Letters. 23: 5403-5406. DOI: 10.1016/0040-4039(82)80141-X |
0.402 |
|
| 1982 |
Boche G, Bernheim M, Schrott W. Primary amines via electrophilic amination of organometallic compounds with o-(diphenylphosphinyl)hydroxylamine Tetrahedron Letters. 23: 5399-5402. DOI: 10.1016/0040-4039(82)80140-8 |
0.384 |
|
| 1982 |
Boche G, Eiben R, Thiel W. Easy Rotation At The Carbon-Carbon Bond In Lithium Cyclopentadienyl (Ester) Enolates Cheminform. 13. DOI: 10.1002/Chin.198250057 |
0.343 |
|
| 1982 |
Boche G, Heidenhain F, Staudigl B. Reactions Of Acceptor‐Substituted Cyclononatetraenyl Anions With Electrophiles: Donor‐Substituted Nonafulvenes And Their Properties Cheminform. 13. DOI: 10.1002/Chin.198248112 |
0.388 |
|
| 1982 |
BOCHE G, HEIDENHAIN F, THIEL W, EIBEN R. ChemInform Abstract: AROMATICITY AS A FUNCTION OF ION-PAIR CHARACTER: ACCEPTOR-SUBSTITUTED CYCLONONATETRAENYL ANIONS, ENOLATE ANIONS WITH VARIABLE CHARGE DISTRIBUTIONS AND UNUSUAL CONFORMATIONAL PROPERTIES Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198248053 |
0.377 |
|
| 1982 |
Boche G, Etzrodt H, Marsch M, Thiel W. The Dianion 1,2-Diphenylbenzocyclobutadienediide Cheminform. 13. DOI: 10.1002/Chin.198221186 |
0.386 |
|
| 1982 |
Boche G, Etzrodt H, Marsch M, Thiel W. The Dianion 1,2,3,4-Tetraphenylcyclobutadienediide Cheminform. 13. DOI: 10.1002/Chin.198221161 |
0.386 |
|
| 1982 |
BOCHE G, FAEHRMANN U. ChemInform Abstract: STEREOSPECIFIC PREPARATION OF (Z)- AND (E)-ISOMERS OF SOME VINYL FLUORIDES Chemischer Informationsdienst. 13. DOI: 10.1002/CHIN.198210107 |
0.275 |
|
| 1982 |
BOCHE G, WINTERMAYR H. ChemInform Abstract: TRIMETHYLENE-RADICAL ANION STEREOISOMERIZATION OF ARYL-SUBSTITUTED CYCLOPROPANES Chemischer Informationsdienst. 13. DOI: 10.1002/CHIN.198204096 |
0.32 |
|
| 1982 |
Boche G, Heidenhain F, Staudigl B. Umsetzungen von Akzeptor-substituierten Cyclononatetraenyl-Anionen mit Elektrophilen: Donor-substituierte Nonafulvene und ihre Eigenschaften Chemische Berichte. 115: 3191-3202. DOI: 10.1002/Cber.19821150922 |
0.418 |
|
| 1982 |
Boche G, Heidenhain F, Thiel W, Eiben R. Aromatizität als Funktion des Ionenpaarcharakters: Akzeptor-substituierte Cyclononatetraenyl-Anionen, Enolat-Anionen mit variablen Ladungsverteilungen und ungewöhnlichen konformativen Eigenschaften Chemische Berichte. 115: 3167-3190. DOI: 10.1002/Cber.19821150921 |
0.426 |
|
| 1982 |
Boche G, Eiben R, Thiel W. Leichte Rotation um die Kohlenstoff‐Kohlenstoff‐Bindung in Lithium‐cyclopentadienyl (ester) enolaten Angewandte Chemie. 21: 1535-1544. DOI: 10.1002/Anie.198215350 |
0.331 |
|
| 1982 |
Boche G, Eiben R, Thiel W. Easy Rotation about the Carbon-Carbon Bond in Lithium Cyclopentadienyl (Ester-)Enolate Angewandte Chemie. 21: 688-689. DOI: 10.1002/Anie.198206881 |
0.346 |
|
| 1982 |
Boche G, Etzrodt H, Marsch M, Thiel W. The Dianion 1,2,3,4‐Tetraphenylcyclobutadienediide Angewandte Chemie. 21: 133-360. DOI: 10.1002/Anie.198201331 |
0.305 |
|
| 1982 |
Boche G, Etzrodt H, Marsch M, Thiel W. The Dianion 1,2‐Diphenylbenzocyclobutadienediide Angewandte Chemie. 21: 132-133. DOI: 10.1002/Anie.198201321 |
0.305 |
|
| 1982 |
Boche G, Etzrodt H, Marsch M, Thiel W. Das Dianion 1,2‐Diphenylbenzocyclobutadiendiid Angewandte Chemie. 94: 141-141. DOI: 10.1002/Ange.19820940220 |
0.322 |
|
| 1981 |
Bernheim M, Boche G. Electrophilic Amination Of Cyclopentadienyllithium Compounds Cheminform. 12. DOI: 10.1002/Chin.198112182 |
0.37 |
|
| 1981 |
Boche G, Fährmann U. Stereospezifische Darstellung der (Z)‐ bzw. (E)‐Isomeren von einigen Vinylfluoriden Chemische Berichte. 114: 4005-4009. DOI: 10.1002/Cber.19811141221 |
0.375 |
|
| 1981 |
Boche G, Wintermayr H. Stereoisomerization of Aryl-Substituted Cyclopropanes via Trimethylene Radical Anions† Angewandte Chemie. 20: 874-876. DOI: 10.1002/Anie.198108741 |
0.398 |
|
| 1981 |
Boche G, Wintermayr H. Stereoisomerisierung arylsubstituierter Cyclopropane via Trimethylen‐Radikalanionen Angewandte Chemie. 93: 923-924. DOI: 10.1002/Ange.19810931032 |
0.367 |
|
| 1980 |
Boche G, Schneider DR, Wintermayr H. Alternative pathways in the reactions of cyclopropyl halides with alkali metal naphthalenes Journal of the American Chemical Society. 102: 5697-5699. DOI: 10.1021/Ja00537A058 |
0.347 |
|
| 1980 |
Boche G, Buckl K, Martens D, Schneider DR. Konformation und Rotation bei Diphenylallyl‐Verbindungen European Journal of Organic Chemistry. 1980: 1135-1171. DOI: 10.1002/Jlac.198019800711 |
0.406 |
|
| 1980 |
Boche G, Schneider DR, Wintermayr H. Alternative pathways in the reactions of cyclopropyl halides with alkali metal naphthalenes Cheminform. 11. DOI: 10.1002/Chin.198046115 |
0.347 |
|
| 1980 |
Boche G, Buckl K, Martens D, Schneider DR. Conformations And Rotational Barriers Of 1,3‐Diphenylallyllithium Compounds Cheminform. 11. DOI: 10.1002/Chin.198043052 |
0.351 |
|
| 1980 |
Bernheim M, Boche G. Electrophilic Amination of Cyclopentadienyllithium Compounds Angewandte Chemie. 19: 1010-1011. DOI: 10.1002/Anie.198010101 |
0.37 |
|
| 1980 |
Bernheim M, Boche G. Elektrophile Aminierung von Cyclopentadienyllithium‐Verbindungen Angewandte Chemie. 92: 1043-1044. DOI: 10.1002/Ange.19800921216 |
0.34 |
|
| 1979 |
Boche G, Heidenhain F. Dynamic equilibrium between ion pairs of aromatic [9]annulene anion and of olefinic nonafulvene structure Journal of the American Chemical Society. 101: 738-739. DOI: 10.1021/Ja00497A043 |
0.374 |
|
| 1979 |
Boche G, Buckl K, Martens D, Schneider DR. Conformation and rotational barriers of 2-substituted 1,3-diphenylallyl anions Tetrahedron Letters. 20: 4967-4970. DOI: 10.1016/S0040-4039(01)86763-0 |
0.36 |
|
| 1979 |
Boche G, Bernheim M, Lawaldt D, Ruisinger B. The facile (<−50°C) formation of cis-bicyclo[6.1.0]nona-2,4,6-trienes from cyclonona-1,3,5,7-tetraenes: A symmetry - forbidden reaction Tetrahedron Letters. 20: 4285-4286. DOI: 10.1016/S0040-4039(01)86567-9 |
0.371 |
|
| 1979 |
Boche G, Heidenhain F, Staudigl B. Substituted cyclononatetraenes and nonafulvenes Tetrahedron Letters. 20: 4201-4204. DOI: 10.1016/S0040-4039(01)86543-6 |
0.38 |
|
| 1979 |
Boche G, Buckl K, Martens D, Schneider DR, Wagner H‐. Ring Opening Of 2,3-Diphenylcyclopropyl- To 1,3-Diphenylallyllithium Compounds Cheminform. 10. DOI: 10.1002/Chin.197947105 |
0.378 |
|
| 1979 |
Boche G, Heidenhain F, Staudigl B. Intermolecular Substituent Exchange Via Ion Pairs By Cyclopentadienyl- And Cyclononatetraenyltrimethylstannane Cheminform. 10. DOI: 10.1002/Chin.197923256 |
0.351 |
|
| 1979 |
Boche G, Heidenhain F. Dynamic Equilibrium Between Ion Pairs Of Aromatic (9)Annulene Anion And Of Olefinic Nonafulvene Structure Cheminform. 10. DOI: 10.1002/Chin.197919111 |
0.374 |
|
| 1979 |
BOCHE G, MARTENS D. ChemInform Abstract: REARRANGEMENT OF THE 9-CYANO-CIS-BICYCLO(6.1.0)NONA-2,4,6-TRIEN-9-YL ANION TO THE 9-CYANOBICYCLO(4.2.1)NONA-2,4,7-TRIEN-9-YL ANION. THE PROBLEM OF BICYCLOAROMATICITY Chemischer Informationsdienst. 10. DOI: 10.1002/CHIN.197913154 |
0.288 |
|
| 1979 |
Boche G, Buckl K, Martens D, Schneider DR, Wagner H. Ringöffnung von 2,3‐Diphenylcyclopropyl‐ zu 1,3‐Diphenyl‐allyllithium‐Verbindungen Chemische Berichte. 112: 2961-2996. DOI: 10.1002/Cber.19791120821 |
0.357 |
|
| 1979 |
Boche G, Martens D. Die Umlagerung des 9-Cyan-cis-bicyclo[6.1.0]nona-2,4,6-trien-9-yl-Anions in das 9-Cyanbicyclo[4.2.1] nona-2,4,7-trien-9-yl-Anion Zur Frage der Bicycloaromatizität Chemische Berichte. 112: 175-195. DOI: 10.1002/Cber.19791120117 |
0.387 |
|
| 1979 |
Boche G, Heidenhain F, Staudigl B. Intermolecular Exchange of Substituents via lons (Ion Pairs) in Cyclopentadienyl‐ and Cyclononatetraenyl‐trimethylstannane Angewandte Chemie. 18: 218-219. DOI: 10.1002/Anie.197902181 |
0.349 |
|
| 1979 |
Boche G, Heidenhain F, Staudigl B. Intermolekularer Substituentenaustausch über Ionen‐(paare) bei Cyclopentadienyl‐ und Cyclononatetraenyl‐trimethylstannan Angewandte Chemie. 91: 228-229. DOI: 10.1002/Ange.19790910310 |
0.354 |
|
| 1978 |
Boche G, Schneider DR. Configurational stability of cyclopropyl radicals in electron-transfer reactions with naphthalene radical anion Tetrahedron Letters. 19: 2327-2330. DOI: 10.1016/S0040-4039(01)91527-8 |
0.379 |
|
| 1978 |
Boche G, Mayer N, Bernheim M, Wagner K. Electrophilic Amination Of ′Carbanions′ With N,N-Dialkyl-O-Arylsulfonylhydroxylamines Cheminform. 9. DOI: 10.1002/Chin.197849149 |
0.381 |
|
| 1978 |
Boche G, Weber H, Martens D, Bieberbach A. Formation Of The Cis,Cis,Cis,Trans-(9)Annulene Anion Cheminform. 9. DOI: 10.1002/Chin.197839127 |
0.351 |
|
| 1978 |
Boche G, Buckl K. Reduction Of 1,3‐Diphenylallyl Anions Via Dianion Radicals To Trianions With Lithium, Sodium, Potassium, And Cesium As Gegenions Cheminform. 9. DOI: 10.1002/Chin.197830126 |
0.369 |
|
| 1978 |
BOCHE G, SCHNEIDER DR. ChemInform Abstract: FORMATION OF THE (Z,E)-1,3-DIPHENYLALLYL RADICAL BY ELECTRON TRANSFER FROM THE (Z,E)-1,3-DIPHENYLALLYL ANION - COMPARISON OF THE ROTATION BARRIERS OF RADICALS AND ANIONS Chemischer Informationsdienst. 9. DOI: 10.1002/CHIN.197809113 |
0.266 |
|
| 1978 |
Boche G, Bieberbach A. Isomerisierung des cis,cis,cis,trans‐[9]Annulen‐Anions Chemische Berichte. 111: 2850-2858. DOI: 10.1002/Cber.19781110811 |
0.387 |
|
| 1978 |
Boche G, Weber H, Martens D, Bieberbach A. Darstellung des cis,cis,cis,trans-[9]Annulen-Anions Chemische Berichte. 111: 2480-2496. DOI: 10.1002/Cber.19781110703 |
0.397 |
|
| 1978 |
Boche G, Mayer N, Bernheim M, Wagner K. Electrophilic Amination of “Carbanions” with N,N-Dialkyl-O-arylsulfonylhydroxylamines†‡ Angewandte Chemie. 17: 687-688. DOI: 10.1002/Anie.197806871 |
0.381 |
|
| 1978 |
Boche G. Book Review: Pericycli Reactions. Vol. I. By A. P. Marchand and R. E. Lehr Angewandte Chemie. 17: 471-471. DOI: 10.1002/Anie.197804711 |
0.349 |
|
| 1978 |
Boche G, Buckl K. Reduction of 1,3‐Diphenylallyl Anions via Dianion Radicals to Trianions with Lithium, Sodium, Potassium, and Cesium as Gegenions Angewandte Chemie. 17: 284-285. DOI: 10.1002/Anie.197802841 |
0.384 |
|
| 1978 |
Boche G, Heidenhain F. Alkali Metal Salts of RC(O)-Substituted Cyclononatetraenyl Anions: Aromatic [9] Annulene Anion or Olefinic Nonafulvene Structure as Function of Gegenion and Solvent† Angewandte Chemie. 17: 283-284. DOI: 10.1002/Anie.197802831 |
0.403 |
|
| 1978 |
Boche G, Mayer N, Bernheim M, Wagner K. Elektrophile Aminierung von „0Carbanionen”︁ mit N,N‐Dialkyl‐O‐arylsulfonylhydroxylaminen Angewandte Chemie. 90: 733-734. DOI: 10.1002/Ange.19780900927 |
0.361 |
|
| 1978 |
Boche G. Pericyclic Reactions. Vol. I. Von A. P. Marchand und R. E. Lehr. Academic Press, Inc., New York—London 1977. 1. Aufl., XI, 286 S., geb. $ 280.00 Angewandte Chemie. 90: 499-500. DOI: 10.1002/Ange.19780900637 |
0.357 |
|
| 1978 |
Boche G, Buckl K. Reduktion von 1,3‐Diphenylallyl‐Anionen über Dianion‐Radikale zu Trianionen mit Lithium, Natrium, Kalium und Caesium als Gegenionen Angewandte Chemie. 90: 291-292. DOI: 10.1002/Ange.19780900417 |
0.338 |
|
| 1978 |
Boche G, Heidenhain F. Alkalimetallsalze RC(O)‐substituierter Cyclononatetraenyl‐Anionen: Aromatische [9]Annulen‐Anion‐ oder olefinische Nonafulven‐Struktur als Funktion von Gegenion und Lösungsmittel Angewandte Chemie. 90: 290-291. DOI: 10.1002/Ange.19780900416 |
0.344 |
|
| 1977 |
BOCHE G, HEIDENHAIN F. ChemInform Abstract: MONOHAPTO-Σ-CYCLONONATETRAENYL DERIVATIVES OF GROUP IV AND V ELEMENTS Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/CHIN.197712255 |
0.217 |
|
| 1977 |
Boche G, Schneider DR. Formation of the (Z,E)‐1,3‐Diphenylallyl Radical from the (Z,E)‐1,3‐Diphenylallyl Anion by Electron Transfer—Comparison of the Rotational Barriers of the Radical and the Anion Angewandte Chemie. 16: 869-870. DOI: 10.1002/Anie.197708691 |
0.364 |
|
| 1976 |
Boche G, Martens D, Wagner HU. Topomerization of the (Z,E)-1,3-diphenyl-2-cyanoallyl anion Journal of the American Chemical Society. 98: 2668-2669. DOI: 10.1021/Ja00425A047 |
0.346 |
|
| 1976 |
Boche G, Schneider DR. 1,3-diphenylallyl anion: preparation of the unstable (Z,E)-isomer Tetrahedron Letters. 17: 3657-3660. DOI: 10.1016/S0040-4039(00)92986-1 |
0.373 |
|
| 1976 |
Boche G, Bieberbach A. Isomerization of the ,,,-[9]annulene anion Tetrahedron Letters. 17: 1021-1024. DOI: 10.1016/S0040-4039(00)77995-0 |
0.408 |
|
| 1976 |
Boche G, Heidenhain F. Monohapto-σ-cyclononatetraenyl-derivate von elementen der IV. und V. hauptgruppe Journal of Organometallic Chemistry. 121. DOI: 10.1016/S0022-328X(00)85096-2 |
0.393 |
|
| 1976 |
Boche G, Bieberbach A. Isomerization of the cis,cis,cis,trans-[9]annulene anion Cheminform. 9: 1021-1024. DOI: 10.1002/Chin.197843105 |
0.349 |
|
| 1976 |
Boche G, Martens D, Wagner HU. Topomerization Of The (Z,E)-1,3-Diphenyl-2-Cyanoallyl Anion Cheminform. 7. DOI: 10.1002/Chin.197628114 |
0.346 |
|
| 1976 |
BOCHE G, SCHNEIDER DR. ChemInform Abstract: (PHENYLTHIO)CYCLOPROPANES BY PHASE TRANSFER CATALYSIS Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/CHIN.197609162 |
0.207 |
|
| 1975 |
Boche G, Schneider DR. Thiophenylcyclopropane durch phasentransfer-katalyse Tetrahedron Letters. 16: 4247-4248. DOI: 10.1016/S0040-4039(00)91161-4 |
0.345 |
|
| 1975 |
Boche G, Bieberbach A, Weber H. Die Topomerisierung Des Cis,Cis,Cis,Trans‐(9)‐Annulen‐Anions Cheminform. 6. DOI: 10.1002/Chin.197541070 |
0.344 |
|
| 1975 |
Boche G, Bieberbach A, Weber H. Topomerization of the cis,cis,cis,trans‐[9]Annulene Anion Angewandte Chemie. 14: 562-563. DOI: 10.1002/Anie.197505621 |
0.344 |
|
| 1975 |
Boche G, Bieberbach A, Weber H. Die Topomerisierung des cis, cis, cis, trans-[9]Annulen-Anions† Angewandte Chemie. 87: 550-551. DOI: 10.1002/Ange.19750871515 |
0.347 |
|
| 1974 |
Boche G, Schneider G. π donor and π acceptor substituent effects in the thermal rearrangement of 9-substituted -bicyclo[6.1.O]nona-2,4,6-trienes ☆ Tetrahedron Letters. 15: 2449-2452. DOI: 10.1016/S0040-4039(01)92283-X |
0.387 |
|
| 1974 |
BOCHE G, SCHNEIDER G. ChemInform Abstract: PI-DONOR AND PI-ACCEPTOR SUBSTITUENT EFFECTS IN THE THERMAL REARRANGEMENT OF 9-SUBSTITUTED CIS-BICYCLO(6,1,0)NONA-2,4,6-TRIENES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/chin.197441223 |
0.278 |
|
| 1974 |
Boche G, Weber H, Benz J. Reaktion Von Cis-Bicyclo(6.1.0)Nona-2,4,6-Trien Mit Tetracyanaethylen Cheminform. 5. DOI: 10.1002/Chin.197421146 |
0.348 |
|
| 1974 |
Boche G, Weber H, Benz J. Reaction of cis-Bicyclo[6.1.0]nona-2,4,6-triene with Tetracyanoethylene† Angewandte Chemie. 13: 207-208. DOI: 10.1002/Anie.197402071 |
0.38 |
|
| 1974 |
Boche G, Weber H, Benz J. Zur Reaktion von cis‐Bicyclo[6.1.0]nona‐2,4,6‐trien mit Tetracyanäthylen Angewandte Chemie. 86: 238-239. DOI: 10.1002/Ange.19740860612 |
0.348 |
|
| 1973 |
Boche G. Book Review: Mechanism in Organic Chemistry. By R. Alder, R. Baker, and J. M. Brown Angewandte Chemie. 12: 680-681. DOI: 10.1002/Anie.197306804 |
0.319 |
|
| 1973 |
Boche G. Mechanism in Organic Chemistry. Von R. W. Alder, R. Baker u. J. M. Brown. John Wiley & Sons, Inc., New York–London 1971. 1. Aufl., X, 378 S., zahlr. Abb., gcb. £ 5.— Angewandte Chemie. 85: 725-725. DOI: 10.1002/Ange.19730851611 |
0.328 |
|
| 1972 |
Boche G, Martens D. Ringoeffnung Eines Cyclopropylanions Und Cycloaddition Des Allylanions Cheminform. 3. DOI: 10.1002/Chin.197244168 |
0.377 |
|
| 1972 |
SZEIMIES G, BOCHE G. ChemInform Abstract: DIE ELEKTROCYCLISCHE UMWANDLUNG DES CYCLOPROPYLRADIKALS IN DAS ALLYLRADIKAL, EINE SEMIEMPIRISCHE SCF-MO-STUDIE Chemischer Informationsdienst. 3. DOI: 10.1002/Chin.197205125 |
0.589 |
|
| 1972 |
BOCHE G, SZEIMIES G. ChemInform Abstract: ELEKTROCYCLISCHE RK. VON RADIKALEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197205124 |
0.582 |
|
| 1972 |
Boche G, Martens D-D. Ring Opening of a Cyclopropyl Anion and Cycloaddition of the Allyl Anion Angewandte Chemie. 11: 724-725. DOI: 10.1002/Anie.197207241 |
0.396 |
|
| 1972 |
Boche G, Martens D-D. Ringöffnung eines Cyclopropylanions und Cycloaddition des Allylanions Angewandte Chemie. 84: 768-769. DOI: 10.1002/Ange.19720841610 |
0.377 |
|
| 1971 |
Schleyer PvR, Barborak JC, Su TM, Boche G, Schneider G. Thermal bicyclo[6.1.0]nonatrienyl chloride-dihydroindenyl chloride rearrangement Journal of the American Chemical Society. 93: 279-281. DOI: 10.1021/Ja00730A063 |
0.347 |
|
| 1971 |
Barborak JC, Su T-, Schleyer PVR, Boche G, Schneider G. Thermische Bicyclo(6,1,0)Nonatrienylchlorid-Dihydroindenylchlorid-Umlagerung Cheminform. 2. DOI: 10.1002/Chin.197113214 |
0.402 |
|
| 1971 |
Szeimies G, Boche G. Electrocyclic Transformation of Cyclopropyl Radical into Allyl Radical: A Semiempirical SCF MO Study Angewandte Chemie International Edition in English. 10: 912-914. DOI: 10.1002/Anie.197109121 |
0.57 |
|
| 1971 |
Boche G, Szeimies G. Electrocyclic Reactions of Radicals Angewandte Chemie International Edition in English. 10: 911-912. DOI: 10.1002/Anie.197109111 |
0.593 |
|
| 1971 |
Szeimies G, Boche G. Die elektrocyclische Umwandlung des Cyclopropylradikals in das Allylradikal: Eine semi-empirische SCF-MO-Studie Angewandte Chemie. 83: 979-980. DOI: 10.1002/Ange.19710832315 |
0.578 |
|
| 1971 |
Boche G, Szeimies G. Elektrocyclische Reaktionen von Radikalen Angewandte Chemie. 83: 978-979. DOI: 10.1002/Ange.19710832314 |
0.566 |
|
| 1970 |
Boche G, Martens D, Danzer W. Trans,Cis,Cis,Cis-Cyclononatetraenyl-Anion, Ein Aromatisches 10Pi-Elektronensyst. Cheminform. 1. DOI: 10.1002/Chin.197010171 |
0.348 |
|
| 1969 |
Van Tamelen EE, Fechter RB, Schneller SW, Boche G, Greeley RH, Akermark B. Titanium(II) in the fixation-reduction of molecular nitrogen under mild conditions Journal of the American Chemical Society. 91: 1551-1552. DOI: 10.1021/Ja01034A057 |
0.318 |
|
| 1969 |
Boche G, Martens D, Danzer W. trans,cis,cis,cis‐Cyclononatetraenyl Anion, a New Aromatic 10 π System Angewandte Chemie. 8: 984-984. DOI: 10.1002/Anie.196909841 |
0.366 |
|
| 1969 |
Boche G, Martens D, Danzer W. trans,cis,cis,cis-Cyclononatetraenyl-Anion, ein neues aromatisches 10π-Elektronensystem Angewandte Chemie. 81: 1003-1004. DOI: 10.1002/Ange.19690812315 |
0.353 |
|
| 1968 |
Tamelen EEv, Boche G, Greeley R. An organic-inorganic system for reaction with nitrogen of the air and operation of a facile nitrogen fixation-reduction cycle Journal of the American Chemical Society. 90: 1677-1678. DOI: 10.1021/Ja01008A066 |
0.347 |
|
| 1968 |
Huisgen R, Boche G, Dahmen A, Hechtl W. Substituenteneinflüsse auf das tautomerie-gleichgewicht cycloocta-1.3.5-trien / bicyclo[4.2.0]octadien Tetrahedron Letters. 9: 5215-5219. DOI: 10.1016/S0040-4039(00)89826-3 |
0.47 |
|
| 1967 |
Tamelen EEV, Boche G, Ela SW, Fechter RB. Direct ammonia formation under mild conditions by molecular nitrogen reducing systems based on organic titanium species Journal of the American Chemical Society. 89: 5707-5708. DOI: 10.1021/Ja00998A039 |
0.325 |
|
| 1967 |
Huisgen R, Boche G, Huber H. Halogenation of cyclooctatetraene via 8-halohomotropylium ions Journal of the American Chemical Society. 89: 3345-3346. DOI: 10.1021/Ja00989A042 |
0.465 |
|
| 1967 |
Boche G, Hechtl W, Huber H, Huisgen R. endo- and exo-8-Chlorohomotropylium salts Journal of the American Chemical Society. 89: 3344-3345. DOI: 10.1021/Ja00989A041 |
0.501 |
|
| 1966 |
Huisgen R, Boche G, Hechtl W, Huber H. Chlorination of Cyclooctatetraene Angewandte Chemie. 5: 585-586. DOI: 10.1002/Anie.196605852 |
0.475 |
|
| 1966 |
Huisgen R, Boche G, Hechtl W, Huber H. Zur Chlorierung des Cyclooctatetraens Angewandte Chemie. 78: 595-595. DOI: 10.1002/Ange.19660781117 |
0.478 |
|
| 1965 |
Boche G, Huisgen R. Polybromide des cyclooctatetraens Tetrahedron Letters. 6: 1775-1777. DOI: 10.1016/S0040-4039(00)90126-6 |
0.477 |
|
| 1965 |
Huisgen R, Boche G. Zum mechanismus der bromierung des cyclooctatetraens Tetrahedron Letters. 6: 1769-1774. DOI: 10.1016/S0040-4039(00)90125-4 |
0.486 |
|
| 1965 |
Huisgen R, Mietzsch F, Boche G, Seidl H. Valence Tautomerism of Unsaturated Ring Systems Angewandte Chemie. 4: 368-368. DOI: 10.1002/Anie.196503681 |
0.477 |
|
| 1965 |
Hulsgen R, Mietzsch F, Boche G, Seidl H. Zur Valenztautomerie ungesättigter Ringsysteme Angewandte Chemie. 77: 353-353. DOI: 10.1002/Ange.19650770726 |
0.332 |
|
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