| Year |
Citation |
Score |
| 2020 |
Hoz S, De S, Gottlieb HE. Quantification of the Interaction of SmI2 with Substrates and Ligands. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32045042 DOI: 10.1002/Chem.201905233 |
0.319 |
|
| 2020 |
Nimkar A, Maity S, Hoz S. Coordination of tridentate ligands to SmI2: cooperativity and incremental effect on reduction potential and on reactivity Pure and Applied Chemistry. 92: 85-96. DOI: 10.1515/Pac-2019-0213 |
0.595 |
|
| 2019 |
Flowers RA, Maity S, Hoz S, Nimkar A. Contrasting Effect of Additives on Photoinduced Reactions of SmI2 Amey Nimkar,[a] Sandeepan Maity,[b] Robert A Flowers II*[b] and Shmaryahu Hoz*[a]. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31150561 DOI: 10.1002/Chem.201901997 |
0.717 |
|
| 2019 |
Maity S, Nimkar A, Hoz S. Task-Dependent Coordination Levels of SmI. The Journal of Organic Chemistry. PMID 30668106 DOI: 10.1021/Acs.Joc.8B02989 |
0.634 |
|
| 2017 |
Flowers RA, Hoz S, Maity S. Aza vs. Oxophilicity of SmI2: A Break of a Paradigm. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29024166 DOI: 10.1002/Chem.201703394 |
0.677 |
|
| 2017 |
Maity S, Hoz S. Pushing SmI2Reactions towards the Limit‐ Entropy Driven Reduction of a Benzene Ring Chemistryselect. 2: 2499-2502. DOI: 10.1002/SLCT.201700214 |
0.529 |
|
| 2015 |
Maity S, Hoz S. Deciphering a 20-Year-Old Conundrum: The Mechanisms of Reduction by the Water/Amine/SmI2 Mixture. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 18394-400. PMID 26525449 DOI: 10.1002/Chem.201503104 |
0.635 |
|
| 2015 |
Yella R, Gottlieb HE, Hoz S. A [2 + 3] Reductive Cyclodimerization of Quinoline by SmI2. The Journal of Organic Chemistry. 80: 8929-32. PMID 26266694 DOI: 10.1021/Acs.Joc.5B01572 |
0.372 |
|
| 2015 |
Yitzhaki O, Hoz S. Reversed Electron Apportionment in Mesolytic Cleavage: The Reduction of Benzyl Halides by SmI2. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 9242-8. PMID 25965697 DOI: 10.1002/Chem.201500519 |
0.41 |
|
| 2014 |
Yella R, Hoz S. Channeling the SmI₂ reactions to the radical path: radicals resisting reduction by SmI₂. Organic Letters. 16: 3876-9. PMID 25030208 DOI: 10.1021/Ol501490F |
0.371 |
|
| 2014 |
Halder S, Hoz S. Hydroxylated HMPA enhances both reduction potential and proton donation in SmI₂ reactions. The Journal of Organic Chemistry. 79: 2682-7. PMID 24559471 DOI: 10.1021/Jo500161S |
0.394 |
|
| 2014 |
Yosipof A, Basch H, Hoz S. Efficiency of electric field catalysis in nucleophilic and electrophilic addition to polyenes Journal of Physical Organic Chemistry. 27: 191-197. DOI: 10.1002/Poc.3261 |
0.367 |
|
| 2013 |
Yella R, Hoz S. Reduction of 4-styrylpyridine by SmI2: an inner sphere electron tranfer case where the binding site differs from the reaction center. Organic Letters. 15: 5262-5. PMID 24098991 DOI: 10.1021/Ol402484J |
0.397 |
|
| 2013 |
Yosipof A, Basch H, Hoz S. Metamorphosis of a transition state into a stable species. The Journal of Physical Chemistry. A. 117: 7737-41. PMID 23886075 DOI: 10.1021/Jp405559H |
0.307 |
|
| 2013 |
Yosipof A, Basch H, Hoz S. Nucleophilic and electrophilic reactions of polyynes catalyzed by an electric field: toward barcoding of carbon nanotubes like long homogeneous substrates. The Journal of Physical Chemistry. A. 117: 5023-7. PMID 23705974 DOI: 10.1021/Jp402758U |
0.314 |
|
| 2012 |
Rao CN, Hoz S. Synergism and inhibition in the combination of visible light and HMPA in SmI2 reductions. The Journal of Organic Chemistry. 77: 9199-204. PMID 23025345 DOI: 10.1021/Jo3017814 |
0.368 |
|
| 2012 |
Whelan J, Abdallah D, Piskorz K, Wojtyk JT, Dust JM, Nunzi JM, Hoz S, Buncel E. Photochemical and thermal spiropyran (SP)-merocyanine (MC) interconversion: a dichotomy in dependence on viscosity. Physical Chemistry Chemical Physics : Pccp. 14: 13684-91. PMID 22968657 DOI: 10.1039/C2Cp42259J |
0.509 |
|
| 2012 |
Rao CN, Hoz S. Photostimulated reduction of nitriles by SmI2. The Journal of Organic Chemistry. 77: 4029-34. PMID 22468753 DOI: 10.1021/Jo300383R |
0.401 |
|
| 2011 |
Rao CN, Hoz S. The effect of replacing carbon by nitrogen in reductions with SmI2: reduction of azobenzene. The Journal of Organic Chemistry. 76: 9438-43. PMID 22004459 DOI: 10.1021/Jo2018153 |
0.382 |
|
| 2011 |
Rao CN, Hoz S. Autocatalysis and surface catalysis in the reduction of imines by SmI2. Journal of the American Chemical Society. 133: 14795-803. PMID 21848327 DOI: 10.1021/Ja205885Q |
0.382 |
|
| 2011 |
Upadhyay SK, Hoz S. The effect of proton donors on the facial stereoselectivity in SmI2 reduction of norcamphor. The Journal of Organic Chemistry. 76: 1355-60. PMID 21250712 DOI: 10.1021/Jo1023206 |
0.632 |
|
| 2009 |
Amiel-Levy M, Hoz S. Guidelines for the use of proton donors in SmI2 reactions: reduction of alpha-cyanostilbene. Journal of the American Chemical Society. 131: 8280-4. PMID 19507909 DOI: 10.1021/Ja9013997 |
0.406 |
|
| 2009 |
Abdallah D, Whelan J, Dust JM, Hoz S, Buncel E. Energy transfer in the azobenzene-naphthalene light harvesting system. The Journal of Physical Chemistry. A. 113: 6640-7. PMID 19456113 DOI: 10.1021/Jp901596T |
0.459 |
|
| 2009 |
Farran H, Hoz S. Reduction of benzophenones with SmI2. Post electron transfer processes. The Journal of Organic Chemistry. 74: 2075-9. PMID 19199659 DOI: 10.1021/Jo802547R |
0.43 |
|
| 2009 |
Pour N, Altus E, Basch H, Hoz S. The Origin of the Auxetic Effect in Prismanes: Bowtie Structure and the Mechanical Properties of Biprismanes. The Journal of Physical Chemistry C. 113: 3467-3470. DOI: 10.1021/Jp809791J |
0.303 |
|
| 2009 |
Rozental E, Hoz S. Intrinsic barrier for protonation of radical anions Tetrahedron. 65: 10945-10949. DOI: 10.1016/J.Tet.2009.10.092 |
0.33 |
|
| 2008 |
Farran H, Hoz S. Quantifying the electrostatic driving force behind SmI2 reductions. Organic Letters. 10: 4875-7. PMID 18855400 DOI: 10.1021/Ol8019692 |
0.371 |
|
| 2008 |
Farran H, Hoz S. On the role of samarium/HMPA in the post electron-transfer steps in SmI2 reductions. Organic Letters. 10: 865-7. PMID 18247497 DOI: 10.1021/Ol7029883 |
0.338 |
|
| 2007 |
Tarnopolsky A, Hoz S. Reductions with SmI2: mechanistic probe for distinguishing between two operational modes of proton transfer. Organic & Biomolecular Chemistry. 5: 3801-4. PMID 18004459 DOI: 10.1039/B713014G |
0.322 |
|
| 2007 |
Wojtyk JTC, Wasey A, Xiao NN, Kazmaier PM, Hoz S, Yu C, Lemieux RP, Buncel E. Elucidating the mechanisms of acidochromic spiropyran-merocyanine interconversion Journal of Physical Chemistry A. 111: 2511-2516. PMID 17388360 DOI: 10.1021/Jp068575R |
0.491 |
|
| 2007 |
Tarnopolsky A, Hoz S. Reduction of activated olefins by SmI2. Detouring the classical Birch mechanism and a negative order in SmI2. Journal of the American Chemical Society. 129: 3402-7. PMID 17319671 DOI: 10.1021/Ja0686662 |
0.342 |
|
| 2006 |
Wolk JL, Rozental E, Basch H, Hoz S. Strain energy release and intrinsic barriers in internal nucleophilic reactions. The Journal of Organic Chemistry. 71: 3876-9. PMID 16674063 DOI: 10.1021/Jo060215C |
0.371 |
|
| 2005 |
Kleiner G, Tarnopolsky A, Hoz S. Reduction of benzophenone by SmI2: the role of proton donors in determining product distribution. Organic Letters. 7: 4197-200. PMID 16146386 DOI: 10.1021/Ol051623Q |
0.343 |
|
| 2005 |
Kiepek E, Zhou Y, Hoz S, Rozental E, Kazmaier PM, Buncel E. Dissociation of the phenanthroimidazole dimer A highly delocalized radical Gomberg revisited Canadian Journal of Chemistry. 83: 1448-1459. DOI: 10.1139/V05-177 |
0.497 |
|
| 2004 |
Wolk JL, Sprecher M, Basch H, Hoz S. Relative reactivity of three and four membered rings--the absence of charge effect. Organic & Biomolecular Chemistry. 2: 1065-9. PMID 15034630 DOI: 10.1039/B314869F |
0.319 |
|
| 2004 |
Sominsky L, Rozental E, Gottlieb H, Gedanken A, Hoz S. Uncatalyzed Meerwein-Ponndorf-Oppenauer-Verley reduction of aldehydes and ketones under supercritical conditions. The Journal of Organic Chemistry. 69: 1492-6. PMID 14987002 DOI: 10.1021/Jo035251F |
0.323 |
|
| 2004 |
Rozental E, Goldberg M, Basch H, Hoz S. Charge transfer complexes between azidopentazole and aromatic nuclei Journal of Molecular Structure: Theochem. 674: 153-157. DOI: 10.1016/J.Theochem.2004.02.001 |
0.313 |
|
| 2004 |
Habusha U, Rozental E, Hoz S. Tuning carbanion reactivity by complexing with boranes: γ‐elimination reaction as a model Journal of Physical Organic Chemistry. 17: 983-989. DOI: 10.1002/Poc.814 |
0.376 |
|
| 2003 |
Palani N, Jayaprakash K, Hoz S. Alkylation of nitroaromatics with trialkyborane. The Journal of Organic Chemistry. 68: 4388-91. PMID 12762741 DOI: 10.1021/Jo034218Q |
0.403 |
|
| 2003 |
Ren Y, Wolk JL, Hoz S. Hybrid DFT study on the gas-phase SN2 reactions at neutral oxygen International Journal of Mass Spectrometry. 225: 167-176. DOI: 10.1016/S1387-3806(02)01113-2 |
0.346 |
|
| 2002 |
Habusha U, Rozental E, Hoz S. Could ionic gamma-elimination be concerted: clocking the internal displacement across a cyclobutane ring. Journal of the American Chemical Society. 124: 15006-11. PMID 12475344 DOI: 10.1021/Ja028644P |
0.357 |
|
| 2002 |
Yi R, Basch H, Hoz S. The periodic table and the intrinsic barrier in SN2 reactions Journal of Organic Chemistry. 67: 5891-5895. PMID 12182618 DOI: 10.1021/Jo020325T |
0.356 |
|
| 2002 |
Grinblat J, Ben-Zion M, Hoz S. Halophilic reactions: anomalies in bromine transfer reactions. Journal of the American Chemical Society. 123: 10738-9. PMID 11674007 DOI: 10.1021/Ja011014N |
0.383 |
|
| 2002 |
Ren Y, Wolk JL, Hoz S. The performance of density function theory in describing gas-phase SN2 reactions at saturated nitrogen International Journal of Mass Spectrometry. 221: 59-65. DOI: 10.1016/S1387-3806(02)00894-1 |
0.319 |
|
| 2002 |
Ren Y, Wolk JL, Hoz S. A G2(+) level investigation of the gas-phase identity nucleophilic substitution at neutral oxygen International Journal of Mass Spectrometry. 220: 1-10. DOI: 10.1016/S1387-3806(02)00733-9 |
0.367 |
|
| 2002 |
Yi R, Hoz S. Enantiomerization of bridged 1,1′-binaphthyls Journal of Physical Organic Chemistry. 15: 782-786. DOI: 10.1002/Poc.540 |
0.32 |
|
| 2002 |
Eliad L, Hoz S. The nitro anomaly and Br�nsted ?nuc values inSN2 reactions on chlorine Journal of Physical Organic Chemistry. 15: 540-543. DOI: 10.1002/Poc.482 |
0.385 |
|
| 2001 |
Wolk JL, Hoz T, Basch H, Hoz S. Quantification of the various contributors to rate enhancement in nucleophilic strain releasing reactions. The Journal of Organic Chemistry. 66: 915-8. PMID 11430113 DOI: 10.1021/Jo001412T |
0.325 |
|
| 2000 |
Shifman A, Sprecher M, Hoz S. A novel borane effect on the C/O alkylation ratio in competing SRN1-SN2 reactions Journal of Physical Organic Chemistry. 13: 105-111. DOI: 10.1002/(Sici)1099-1395(200002)13:2<105::Aid-Poc217>3.0.Co;2-W |
0.384 |
|
| 1999 |
Basch H, Hoz T, Hoz S. Hyperconjugative Effects in Carbenium and Silicenium Ions The Journal of Physical Chemistry A. 103: 6458-6467. DOI: 10.1021/Jp991083C |
0.315 |
|
| 1999 |
Hoz S, Basch H, Wolk JL, Hoz T, Rozental E. Intrinsic Barriers in Identity SN2 Reactions and the Periodic Table Journal of the American Chemical Society. 121: 7724-7725. DOI: 10.1021/Ja984315E |
0.353 |
|
| 1998 |
Sella A, Cohen S, Hoz S. 1,3-Diphenylsulphonylcyclobutane: an unprecedented case of a higher stability of the trans isomer of 1,3-disubstituted cyclobutane Canadian Journal of Chemistry. 76: 828-831. DOI: 10.1139/V98-067 |
0.307 |
|
| 1998 |
Tarkka RM, Um I, Xie H, Chatrouse A, Terrier F, Hoz S, Buncel E. Effect of solvent composition on the acidity of phenols in dimethyl sulfoxide-water mixtures Journal of Physical Organic Chemistry. 11: 847-852. DOI: 10.1002/(SICI)1099-1395(199812)11:12<847::AID-POC42>3.0.CO;2-5 |
0.383 |
|
| 1998 |
Tarkka RM, Um IH, Xie HQ, Chatrouse AP, Terrier F, Hoz S, Buncel E. Effect of solvent composition on the acidity of phenols in dimethyl sulfoxide - water mixtures Journal of Physical Organic Chemistry. 11: 847-852. DOI: 10.1002/(Sici)1099-1395(199812)11:12<847::Aid-Poc42>3.0.Co;2-5 |
0.483 |
|
| 1997 |
Yacovan A, Hoz S. Reactions of SmI(2) with Nitro Olefins. The Journal of Organic Chemistry. 62: 771-772. PMID 11671484 DOI: 10.1021/Jo961608M |
0.384 |
|
| 1997 |
Basch H, Hoz S. Ab InitioStudy of Hydrogen Abstraction Reactions The Journal of Physical Chemistry A. 101: 4416-4431. DOI: 10.1021/Jp970011N |
0.365 |
|
| 1996 |
Hoz S, Liu P, Buncel E. Conflicting evidence regarding the mechanism of the sulfonyl transfer reaction Chemical Communications. 995-996. DOI: 10.1039/Cc9960000995 |
0.531 |
|
| 1996 |
Hoz S, Azran C, Sella A. Atomic Motions and Protonation Stereochemistry in Nucleophilic Additions to Bicyclobutanes1 Journal of the American Chemical Society. 118: 5456-5461. DOI: 10.1021/Ja960370G |
0.345 |
|
| 1996 |
Sella A, Basch H, Hoz S. Reactivity of Strained Compounds: Is Ground State Destabilization the Major Cause for Rate Enhancement?1 Journal of the American Chemical Society. 118: 416-420. DOI: 10.1021/Ja951408C |
0.409 |
|
| 1996 |
Yacovan A, Hoz S, Bilkis I. Reactions of SmI2with Olefins: Mechanism and Complexation Effect on Chemoselectivity Journal of the American Chemical Society. 118: 261-262. DOI: 10.1021/Ja950937D |
0.365 |
|
| 1995 |
Azran C, Hoz S. Bridgehead substituents effect on the reactivity of bicyclobutane in its reactions with nucleophiles. A comparison with olefinic systems Tetrahedron. 51: 11421-11430. DOI: 10.1016/0040-4020(95)00706-E |
0.351 |
|
| 1994 |
Tarkka RM, Park WKC, Liu P, Buncel E, Hoz S. Solvent independent transition-state structures. Part III. Sulfonyl transfer reactions Journal of the Chemical Society, Perkin Transactions 2. 2439-2444. DOI: 10.1039/P29940002439 |
0.567 |
|
| 1993 |
Buncel E, Tarkka R, Hoz S. The phenomenology of differently constructed Brønsted-type plots Journal of the Chemical Society, Chemical Communications. 109-110. DOI: 10.1039/C39930000109 |
0.481 |
|
| 1993 |
Hoz S. Is the transition state indeed intermediate between reactants and products? The Michael addition reaction as a case study Accounts of Chemical Research. 26: 69-74. DOI: 10.1021/Ar00026A006 |
0.346 |
|
| 1993 |
Basch H, Hoz S, Goldberg M. Energy Trapping in Dications Israel Journal of Chemistry. 33: 403-414. DOI: 10.1002/Ijch.199300047 |
0.301 |
|
| 1992 |
Gross Z, Hoz S. Curve crossing analysis of LFER data in Michael addition reactions Canadian Journal of Chemistry. 70: 1022-1027. DOI: 10.1139/V92-136 |
0.533 |
|
| 1991 |
Hoz S, Basch H, Wolk JL, Rappoport Z, Goldberg M. Calculated double-bond stabilization by bromine and chlorine. Relevance to the kBr/kCl element effect The Journal of Organic Chemistry. 56: 5424-5426. DOI: 10.1021/Jo00018A042 |
0.484 |
|
| 1991 |
Gross Z, Hoz S. Curve crossing analysis and rate - 13C chemical shift correlation in Michael reaction. Tetrahedron Letters. 32: 5163-5166. DOI: 10.1016/S0040-4039(00)93456-7 |
0.538 |
|
| 1991 |
Basch H, Hoz S, Goldberg M, Gamss L. Electronic Structure and Properties of the O2+2, SO2+and S2+2Diatomic Dications Israel Journal of Chemistry. 31: 335-343. DOI: 10.1002/Ijch.199100038 |
0.301 |
|
| 1990 |
Wolk JL, Hajnal MR, Hoz S, Tarkka RM, Buncel E. Relative reactivity of three oxygen lone pairs of an α-nucleophile in SN2 reactions Canadian Journal of Chemistry. 68: 1182-1185. DOI: 10.1139/V90-182 |
0.526 |
|
| 1990 |
Haboosha U, Hoz S. Cyclobutane-bicyclobutane system. 16. Effective molarities and ionic chain mechanism in the reaction of a bifunctional nucleophile with substituted bicyclobutane The Journal of Organic Chemistry. 55: 2090-2094. DOI: 10.1021/Jo00294A022 |
0.424 |
|
| 1990 |
Hoz S, Wolk J. Stabilization of carbenium ions by an α-azido group Tetrahedron Letters. 31: 4085-4088. DOI: 10.1016/S0040-4039(00)94506-4 |
0.305 |
|
| 1989 |
Buncel E, Um IH, Hoz S. Solvent-independent transition-state structure for acyl-transfer reactions. A novel strategy for construction of a Broensted correlation Journal of the American Chemical Society. 111: 971-975. DOI: 10.1021/Ja00185A029 |
0.528 |
|
| 1989 |
Hoz S, E B. An AM1 Study of an α-Nucleophile: Geometries and Interconversion Modes of Oximate Anion Stereomers Tetrahedron. 45: 3663-3672. DOI: 10.1016/S0040-4020(01)89228-0 |
0.339 |
|
| 1989 |
Wolfe S, Livneh M, Cohen D, Hoz S. The Ambident Nucleophilic Center. Stereochemical Consequences of HOMO‐LUMO and HOMO‐HOMO Dominant Processes Israel Journal of Chemistry. 29: 221-227. DOI: 10.1002/Ijch.198900030 |
0.375 |
|
| 1989 |
GROSS Z, HOZ S. ChemInform Abstract: Nucleophilic Attacks on Low LUMO Compound. Part 5. Radical-Anionic Nature of the Transition State (III) in the Michael Addition Reaction. Cheminform. 20. DOI: 10.1002/chin.198907094 |
0.515 |
|
| 1988 |
Gross Z, Hoz S. Nucleophilic attacks on low LUMO compounds. Part 5. Radical-anionic nature of the transition state in the Michael addition reaction Journal of the American Chemical Society. 110: 7489-7493. DOI: 10.1021/Ja00230A035 |
0.528 |
|
| 1987 |
Hoz S, Livneh M. Conversion of cyclobutane to bicyclobutane by base-catalyzed 1,3-dehydrohalogenation reaction: a mechanistic study Journal of the American Chemical Society. 109: 7483-7488. DOI: 10.1021/Ja00258A038 |
0.386 |
|
| 1985 |
Hoz S, Dunn EJ, Buncel E, Bannard RAB, Purdon JG. A NOVEL SUBSTITUENT EFFECT ON 31P NMR CHEMICAL SHIFTS IN THE ARYL DIPHENYLPHOSPHINATE SERIES Phosphorus and Sulfur and the Related Elements. 24: 321-326. DOI: 10.1080/03086648508074244 |
0.407 |
|
| 1985 |
Hoz S, Gross Z, Speizman D. Nucleophilic attacks on LL (low LUMO) substrates. Part 3. Molecular stacking of 9-methylenefluorene derivatives as a source of zero-order reactions Journal of the Chemical Society-Perkin Transactions 1. 16: 1143-1146. DOI: 10.1039/P29850001143 |
0.559 |
|
| 1985 |
Hoz S, Aurbach D. Formation and stability of alkoxyimidates in the cyclobutane bicyclobutane system Tetrahedron. 41: 1307-1313. DOI: 10.1016/S0040-4020(01)96532-9 |
0.539 |
|
| 1985 |
Hoz S, Levy R. Cyclobutane-bicyclobutane system: Part 10. Conformation and stability of 1-bicyclobutylcarbinyl anion Journal of Molecular Structure-Theochem. 121: 93-99. DOI: 10.1016/0166-1280(85)85055-7 |
0.312 |
|
| 1985 |
HOZ S, GROSS Z, SPEIZMAN D. ChemInform Abstract: NUCLEOPHILIC ATTACKS ON LL (LOW LUMO) SUBSTRATES. PART 3. MOLECULAR STACKING OF 9-METHYLENEFLUORENE DERIVATIVES AS A SOURCE OF ZERO-ORDER REACTIONS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198548086 |
0.496 |
|
| 1985 |
HOZ S, GROSS Z, COHEN D. ChemInform Abstract: THE Π NUCLEOPHILICITY: THE EFFECT OF CHARGE DELOCALIZATION ON THE EFFICIENCY OF INTERNAL DISPLACEMENTS IN ELCB REACTIONS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198532072 |
0.512 |
|
| 1985 |
Hoz S, Gross Z, Cohen D. The .pi. nucleophilicity: the effect of charge delocalization on the efficiency of internal displacements in ElcB reactions The Journal of Organic Chemistry. 50: 832-836. DOI: 10.1002/Chin.198532072 |
0.549 |
|
| 1985 |
HOZ S, AURBACH D. ChemInform Abstract: CYCLOBUTANE-BICYCLOBUTANE SYSTEM. 8. NUCLEOPHILIC “ADDITION-ELIMINATION” DISPLACEMENTS ON ACTIVATED BICYCLOBUTANES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198518149 |
0.432 |
|
| 1985 |
HOZ S, AURBACH D. ChemInform Abstract: CYCLOBUTANE-BICYCLOBUTANE SYSTEM. 2. IONIC BICYCLOBUTANE AS AN INTERMEDIATE IN THE REACTION OF PHS- WITH 3-HALOBICYCLOBUTANECARBONITRILE: COMPARISON BETWEEN THIO- AND OXYCARBENIUM IONS Chemischer Informationsdienst. 16. DOI: 10.1002/chin.198511133 |
0.423 |
|
| 1984 |
Hoz S, Aurbach D. An unusual case of proton removal from an oxacarbenium ion Journal of the Chemical Society, Chemical Communications. 364-365. DOI: 10.1039/C39840000364 |
0.436 |
|
| 1984 |
Hoz S, Aurbach D. Cyclobutane-bicyclobutane system. 8. Nucleophilic "addition-elimination" displacements on activated bicyclobutanes The Journal of Organic Chemistry. 49: 4144-4147. DOI: 10.1021/Jo00196A008 |
0.417 |
|
| 1984 |
Hoz S, Buncel E. Pitfalls in the determination of the α-effect by a two-point analysis. The effect of solvent on the α-effect. Tetrahedron Letters. 25: 3411-3414. DOI: 10.1016/S0040-4039(01)91033-0 |
0.474 |
|
| 1984 |
Hoz S, Aurbach D. Cyclobutane-bicyclobutane system. 2. Ionic bicyclobutane as an intermediate in the reaction of PhS- with 3-halobicyclobutanecarbonitrile: comparison between thio- and oxycarbenium ions The Journal of Organic Chemistry. 49: 3285-3291. DOI: 10.1002/Chin.198511133 |
0.483 |
|
| 1984 |
HOZ S, AURBACH D. ChemInform Abstract: AN UNUSUAL CASE OF PROTON REMOVAL FROM AN OXOCARBENIUM ION Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198429142 |
0.436 |
|
| 1984 |
Hoz S, Aurbach D. Cyclobutane-bicyclobutane systems. 5. Zwitterionic bicyclobutane: an intermediate in the course of nucleophilic vinylic-like substitution reaction on 3-halobicyclobutanecarbonitrile Cheminform. 15. DOI: 10.1002/Chin.198413098 |
0.517 |
|
| 1983 |
Buncel E, Hoz S. Can ground-state destabilization of an α-nucleophile induce an α-effect? Tetrahedron Letters. 24: 4777-4780. DOI: 10.1016/S0040-4039(00)94005-X |
0.472 |
|
| 1983 |
Hoz S, Aurbach D, Avivi C. An unexpected β-elimination from 3,3-Difluorocyclobutanecarbonitrile. Tetrahedron Letters. 24: 1639-1640. DOI: 10.1016/S0040-4039(00)81731-1 |
0.455 |
|
| 1983 |
HOZ S, AURBACH D, AVIVI C. ChemInform Abstract: CYCLOBUTANE-BICYCLOBUTANE SYSTEM. PART 4. AN UNEXPECTED β-ELIMINATION FROM 3,3-DIFLUOROCYCLOBUTANECARBONITRILE Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198331177 |
0.407 |
|
| 1981 |
Hoz S, Speizman D, Feit B, Djamal G, Melamed U. Disproportionation in a Michael addition reaction The Journal of Organic Chemistry. 46: 450-452. DOI: 10.1021/Jo00315A044 |
0.386 |
|
| 1980 |
Hoz S, Aurbach D. Cyclobutane-bicyclobutane system. 3. Free, hydrogen-bonded, and cation-stabilized carbanions .alpha. to a cyano group in a cyclobutane ring Journal of the American Chemical Society. 102: 2340-2345. DOI: 10.1021/Ja00527A035 |
0.441 |
|
| 1979 |
Hoz S, Speizman D. An unusual reaction of azide with nitroolefins Tetrahedron Letters. 20: 4855-4856. DOI: 10.1016/S0040-4039(01)86731-9 |
0.381 |
|
| 1979 |
Hoz S, Haltovsky D. A search for a β effect: the nucleophilicity of the methylene glycolate anion Tetrahedron. 35: 2049-2052. DOI: 10.1016/S0040-4020(01)88977-8 |
0.329 |
|
| 1979 |
Hoz S, Aurbach D. Cyclobutane-bicyclobutane system—I Tetrahedron. 35: 881-883. DOI: 10.1016/0040-4020(79)80110-6 |
0.516 |
|
| 1977 |
A. Frimer A, Rosenthal I, Hoz S. The reaction of superoxide anion radical with electron poor olefins Tetrahedron Letters. 18: 4631-4634. DOI: 10.1016/S0040-4039(01)83587-5 |
0.37 |
|
| 1975 |
HOZ S, ALBECK M, RAPPOPORT Z. Fluoride Ion as a Catalyst for Michael Additions to Nitro-Alkenes Synthesis. 1975: 162-162. DOI: 10.1055/S-1975-23689 |
0.45 |
|
| 1975 |
Albeck M, Hoz S, Rappoport Z. E1cB and E2cB mechanisms in the elimination of trifluoroethoxide ion from α,α-dinitro-β,β-diphenyl-β-(trifluoroethoxy)ethanide anion and the non-reactivity of the β-cyano-α,α-dinitro-β,β-diphenylethanide anion Journal of the Chemical Society-Perkin Transactions 1. 628-637. DOI: 10.1039/P29750000628 |
0.504 |
|
| 1975 |
Rappoport Z, Hoz S. Nucleophilic attacks on carbon–carbon double bonds. Part XXI. Substitution of (E)-α-chloro-β-nitrostyrene by anilines in acetonitrile Journal of the Chemical Society-Perkin Transactions 1. 6: 272-277. DOI: 10.1039/P29750000272 |
0.562 |
|
| 1975 |
ALBECK M, HOZ S, RAPPOPORT Z. ChemInform Abstract: E1CB AND E2CB MECHANISMS IN THE ELIMINATION OF TRIFLUOROETHOXIDE ION FROM ALPHA,ALPHA-DINITRO-BETA,BETA-DIPHENYL-BETA-(TRIFLUOROETHOXY)ETHANIDE ANION AND THE NON-REACTIVITY OF THE BETA-CYANO-ALPHA,ALPHA-DINITRO-BETA-,BETA-DIPHENYLETHA Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197530133 |
0.419 |
|
| 1975 |
HOZ S, ALBECK M, RAPPOPORT Z. ChemInform Abstract: FLUORIDE ION AS A CATALYST FOR MICHAEL ADDITION TO NITRO-ALKENES Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197524134 |
0.392 |
|
| 1975 |
RAPPOPORT Z, HOZ S. ChemInform Abstract: NUCLEOPHILIC ATTACKS ON CARBON-CARBON DOUBLE BONDS PART 21, SUBSTITUTION OF (E)-ALPHA-CHLORO-BETA-NITROSTYRENE BY ANILINES IN ACETONITRILE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/chin.197520125 |
0.399 |
|
| 1972 |
Albeck M, Hoz S, Rappoport Z. E1cB eliminations. Substituent and solvent effects on the E1cB elimination of the second type from 2-aryl-1,1,2-tricyanopropanes Journal of the Chemical Society-Perkin Transactions 1. 1248-1255. DOI: 10.1039/P29720001248 |
0.575 |
|
| 1972 |
Hoz S, Albeck M, Rappoport Z. A very slow ElcB elimination under extreme ElcB conditions Tetrahedron Letters. 13: 3511-3514. DOI: 10.1016/S0040-4039(01)94086-9 |
0.428 |
|
| 1972 |
HOZ S, ALBECK M, RAPPOPORT Z. ChemInform Abstract: EINE SEHR LANGSAME E1CB-ELIMINIERUNG UNTER EXTREMEN E1CB-BEDINGUNGEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197249174 |
0.464 |
|
| 1972 |
ALBECK M, HOZ S, RAPPOPORT Z. ChemInform Abstract: E1CB-ELIMINIERUNGEN, SUBSTITUENTEN- UND LOESUNGSMITTELEINFLUESSE AUF DIE E1CB-ELIMINIERUNG DES ZWEITEN TYPS AUS 2-ARYL-1,1,2-TRICYAN-PROPANEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197240134 |
0.467 |
|
| Show low-probability matches. |