S. Hoz

发表

INTRINSIC BARRIERS IN IDENTITY SN2 REACTIONS AND THE PERIODIC TABLE

H. Basch, T. Hoz, S. Hoz, 1999 .

Hybrid DFT study on the gas-phase SN2 reactions at neutral oxygen

Yi Ren, S. Hoz, J. L. Wolk, 2003 .

Acylation or phosphorylation of hydroxyurea unexpectedly takes place on N rather than on O, leading to the formation of amides instead of the expected esters

D. Major, H. Gottlieb, A. Nudelman, 2015 .

The .alpha. effect: on the origin of transition-state stabilization

S. Hoz, 1982 .

Can ground-state destabilization of an α-nucleophile induce an α-effect?

E. Buncel, S. Hoz, 1983 .

Pitfalls in the determination of the α-effect by a two-point analysis. The effect of solvent on the α-effect.

E. Buncel, S. Hoz, 1984 .

Solvent-independent transition-state structure for acyl-transfer reactions. A novel strategy for construction of a Broensted correlation

E. Buncel, I. Um, S. Hoz, 1989 .

Alkylation of Nitroaromatics with Trialkylborane

A. Shifman, S. Hoz, N. Palani, 2000 .

A novel borane effect on the C/O alkylation ratio in competing SRN1–SN2 reactions

M. Sprecher, S. Hoz, Ana Shifman, 2000 .

A quantitative study of the photostimulated reaction of iodobenzene with diethyl phosphite ion

J. Bunnett, S. Hoz, 1977 .

Photochemical and thermal spiropyran (SP)-merocyanine (MC) interconversion: a dichotomy in dependence on viscosity.

J. Nunzi, James T. C. Wojtyk, E. Buncel, 2012, Physical chemistry chemical physics : PCCP.

Ab Initio Study of Hydrogen Abstraction Reactions

H. Basch, S. Hoz, 1997 .

A Valence bond description of bond dissociation energy curves

P. Aped, H. Basch, S. Hoz, 1996 .

Guidelines for the use of proton donors in SmI2 reactions: reduction of alpha-cyanostilbene.

S. Hoz, Mazal Amiel-Levy, 2009, Journal of the American Chemical Society.

Intrinsic barrier for protonation of radical anions

S. Hoz, Esther Rozental, 2009 .

Samarium Iodide Showcase: Unraveling the Mechanistic Puzzle

S. Hoz, 2020, Accounts of chemical research.

Quantification of the Interaction of SmI2 with Substrates and Ligands.

H. Gottlieb, Suranjan De, S. Hoz, 2020, Chemistry.

Contrasting Effect of Additives on Photoinduced Reactions of SmI2 Amey Nimkar,[a] Sandeepan Maity,[b] Robert A Flowers II*[b] and Shmaryahu Hoz*[a].

S. Hoz, Sandeepan Maity, R. A. Flowers, 2019, Chemistry.

Contrasting Effect of Additives on Photoinduced Reactions of SmI 2

S. Hoz, Sandeepan Maity, R. A. Flowers, 2019, Chemistry – A European Journal.

Pushing SmI2 Reactions towards the Limit‐ Entropy Driven Reduction of a Benzene Ring

S. Hoz, Sandeepan Maity, 2017 .

Aza versus Oxophilicity of SmI2 : A Break of a Paradigm.

S. Hoz, Sandeepan Maity, R. A. Flowers, 2017, Chemistry.

Reversed Electron Apportionment in Mesolytic Cleavage: The Reduction of Benzyl Halides by SmI2.

S. Hoz, Offir Yitzhaki, 2015, Chemistry.

Channeling the SmI₂ reactions to the radical path: radicals resisting reduction by SmI₂.

S. Hoz, R. Yella, 2014, Organic letters.

Reductions with SmI2: mechanistic probe for distinguishing between two operational modes of proton transfer.

A. Tarnopolsky, S. Hoz, 2007, Organic & biomolecular chemistry.

Reactions of SmI2 with Olefins: Mechanism and Complexation Effect on Chemoselectivity

I. Bilkis, A. Yacovan, S. Hoz, 1996 .

Hydroxylated HMPA enhances both reduction potential and proton donation in SmI₂ reactions.

S. Halder, S. Hoz, 2014, The Journal of organic chemistry.

On the role of samarium/HMPA in the post electron-transfer steps in SmI2 reductions.

S. Hoz, H. Farran, 2008, Organic letters.

Reduction of benzophenone by SmI2: the role of proton donors in determining product distribution.

A. Tarnopolsky, S. Hoz, Gregory Kleiner, 2005, Organic letters.

The effect of proton donors on the facial stereoselectivity in SmI2 reduction of norcamphor.

S. Hoz, S. K. Upadhyay, 2011, The Journal of organic chemistry.

The effect of replacing carbon by nitrogen in reductions with SmI2: reduction of azobenzene.

S. Hoz, C. Rao, 2011, The Journal of organic chemistry.

Autocatalysis and surface catalysis in the reduction of imines by SmI2.

S. Hoz, C. Rao, 2011, Journal of the American Chemical Society.

Broadening the scope of photostimulated SmI(2) reductions.

S. Hoz, Mazal Amiel-Levy, 2010, Chemistry.

Reduction of benzophenones with SmI2. Post electron transfer processes.

S. Hoz, H. Farran, 2009, The Journal of organic chemistry.

Photostimulated reduction of nitriles by SmI2.

S. Hoz, C. Rao, 2012, The Journal of organic chemistry.

Synergism and inhibition in the combination of visible light and HMPA in SmI2 reductions.

S. Hoz, C. Rao, 2012, The Journal of organic chemistry.

Reduction of activated olefins by SmI2. Detouring the classical Birch mechanism and a negative order in SmI2.

A. Tarnopolsky, S. Hoz, 2007, Journal of the American Chemical Society.

Quantifying the electrostatic driving force behind SmI2 reductions.

S. Hoz, H. Farran, 2008, Organic letters.

Reduction of 4-styrylpyridine by SmI2: an inner sphere electron tranfer case where the binding site differs from the reaction center.

S. Hoz, R. Yella, 2013, Organic letters.

Computational design of biofuels from terpenes and terpenoids

D. Major, S. Hoz, Efrat Pahima, 2019, Sustainable Energy & Fuels.

Harder than diamond: determining the cross-sectional area and Young's modulus of molecular rods.

H. Basch, E. Altus, S. Hoz, 2005, Angewandte Chemie.

Efficiency of electric field catalysis in nucleophilic and electrophilic addition to polyenes

H. Basch, Abraham Yosipof, S. Hoz, 2014 .

Nucleophilic and electrophilic reactions of polyynes catalyzed by an electric field: toward barcoding of carbon nanotubes like long homogeneous substrates.

H. Basch, Abraham Yosipof, S. Hoz, 2013, The journal of physical chemistry. A.

Shaping Polyyne Rods by Using an Electric Field

D. Major, E. Altus, S. Hoz, 2017, ChemistryOpen.

Is the transition state indeed intermediate between reactants and products? The Michael addition reaction as a case study

S. Hoz, 1993 .

CHARGE DISTRIBUTION IN DIACETYLENE, CYANOACETYLENE AND ETHYLACETYLENE ANIONS

P. Aped, S. Hoz, 1997 .

Metamorphosis of a transition state into a stable species.

H. Basch, Abraham Yosipof, S. Hoz, 2013, The journal of physical chemistry. A.

Cooperative Intrinsic Basicity and Hydrogen Bonding Render SmI2 More Azaphilic than Oxophilic

D. Major, R. Schwartz, S. Hoz, 2022, ACS omega.

Fluoride Ion as a Catalyst for Michael Additions to Nitro-Alkenes

Z. Rappoport, M. Albeck, S. Hoz, 1975 .

Alkylation of nitroaromatics with trialkyborane.

K. Jayaprakash, S. Hoz, N. Palani, 2003, The Journal of organic chemistry.

Uncatalyzed Meerwein-Ponndorf-Oppenauer-Verley reduction of aldehydes and ketones under supercritical conditions.

H. Gottlieb, A. Gedanken, S. Hoz, 2004, Journal of Organic Chemistry.

An unusual reaction of azide with nitroolefins

S. Hoz, D. Speizman, 1979 .

An AM1 study of an α-nucleophile: geometries and interconversion modes of oximate anion stereomers

E. Buncel, S. Hoz, 1989 .

Cyclobutane-bicyclobutane system—I : The relative reactivity of the central bond in bicyclobutanecarbonitrile and the double bond in crotononitrile in nucleophilic reactions

D. Aurbach, S. Hoz, 1979 .

Formation and stability of alkoxyimidates in the cyclobutane bicyclobutane system

D. Aurbach, S. Hoz, 1985 .

Reactions of SmI2 with Nitro Olefins

A. Yacovan, S. Hoz, 1997 .

Cyclobutane-bicyclobutane system. 3. Free, hydrogen-bonded, and cation-stabilized carbanions .alpha. to a cyano group in a cyclobutane ring

D. Aurbach, S. Hoz, 1980 .

Deciphering a 20-Year-Old Conundrum: The Mechanisms of Reduction by the Water/Amine/SmI2 Mixture.

S. Hoz, Sandeepan Maity, 2015, Chemistry.

Tuning carbanion reactivity by complexing with boranes: γ-elimination reaction as a model

S. Hoz, Esther Rozental, Uri Habusha, 2004 .

Curve crossing analysis of LFER data in Michael addition reactions

Z. Gross, S. Hoz, 1992 .

A [2 + 3] Reductive Cyclodimerization of Quinoline by SmI2.

H. Gottlieb, S. Hoz, R. Yella, 2015, The Journal of organic chemistry.

The Ambident Nucleophilic Center. Stereochemical Consequences of HOMO‐LUMO and HOMO‐HOMO Dominant Processes

Drora. Cohen, S. Wolfe, S. Hoz, 1989 .

The α-Effect: A Critical Examination of the Phenomenon and Its Origin

Shmaryahu Hoz, E. Buncel, E. Buncel, 1985 .

A novel substituent effect on 31P NMR chemical shifts in the aryl diphenylphosphinate series

E. Buncel, R. Bannard, J. Purdon, 1985 .

Nucleophilic attacks on activated 9-methylenefluorenes. Application of the Ritchie equation to low-lying LUMO substrates

S. Hoz, D. Speizman, 1983 .

Resonance in formamide: resolution of contending models

H. Basch, S. Hoz, 1998 .

Elucidating the mechanisms of acidochromic spiropyran-merocyanine interconversion.

Chen Yu, James T. C. Wojtyk, R. Lemieux, 2007, The journal of physical chemistry. A.

EFFECT OF SOLVENT COMPOSITION ON THE ACIDITY OF PHENOLS IN DIMETHYL SULFOXIDE - WATER MIXTURES

E. Buncel, I. Um, F. Terrier, 1998 .

Inducing chirality ex nihilo by an electric field

S. Hoz, J. L. Wolk, 2015 .

Enantiomerization of bridged 1,1′‐binaphthyls

R. Yi, S. Hoz, 2002 .

Nucleophilic attacks on low LUMO compounds. Part 5. Radical-anionic nature of the transition state in the Michael addition reaction

Z. Gross, S. Hoz, 1988 .

The reaction of superoxide anion radical with electron poor olefins

A. Frimer, I. Rosenthal, S. Hoz, 1978 .

Formation of Formaldehyde in the Thermal Decomposition of D‐Glucose Labelled with 14C at Various Positions

S. Hoz, Y. Houminer, 1970 .

An unexpected β-elimination from 3,3-Difluorocyclobutanecarbonitrile.

D. Aurbach, C. Avivi, S. Hoz, 1983 .

Curve crossing analysis and rate - 13C chemical shift correlation in Michael reaction.

Z. Gross, S. Hoz, 1991 .

The nitro anomaly and Brønsted βnuc values in SN2 reactions on chlorine

Linoam Eliad, S. Hoz, 2002 .

Barrier widths, barrier heights, and the origins of anomalous kinetic H/D isotope effects

Chan Kyung Kim, S. Wolfe, K. Yang, 1990 .

Solvent independent transition-state structures. Part III. Sulfonyl transfer reactions

Ping Liu, E. Buncel, S. Hoz, 1994 .

A search for a β effect: the nucleophilicity of the methylene glycolate anion

S. Hoz, Dvora Haltovsky, 1979 .

Electronic Structure and Properties of the O2+2, SO2+ and S2+2 Diatomic Dications

M. Goldberg, H. Basch, L. Gamss, 1991 .

Energy Trapping in Dications

M. Goldberg, H. Basch, S. Hoz, 1993 .

Hyperconjugative Effects in Carbenium and Silicenium Ions

H. Basch, S. Hoz, and Tova Hoz, 1999 .

THE ENOL OF ACETOACETIC ACID: A COMPUTATIONAL STUDY OF THE RELATIVE STABILITIES OF THE KETONE AND CARBOXYLIC ACID ISOMERS

A. Kresge, S. Hoz, 1997 .

Stabilization of carbenium ions by an α-azido group

S. Hoz, J. L. Wolk, 1990 .

Ab Intio Valence bond description of diatomic dications

M. Goldberg, P. Aped, S. Hoz, 1999 .

Valence bond energy curves for He22

P. Aped, H. Basch, S. Hoz, 1996 .

Charge oscillation in the homolysis of MeX derivatives

M. Goldberg, H. Basch, S. Hoz, 1992 .

Auxetics at the molecular level: a negative poisson's ratio in molecular rods.

N. Pour, H. Basch, E. Altus, 2006, Angewandte Chemie.

The performance of density function theory in describing gas-phase SN2 reactions at saturated nitrogen

Yi Ren, Joel L. Wolk, Yi Ren, 2002 .

Bicyclo[1.1.0]Butane

S. Hoz, 2005 .

Energy transfer in the azobenzene-naphthalene light harvesting system.

E. Buncel, J. Dust, J. Whelan, 2009, The journal of physical chemistry. A.

Cyclobutane-bicyclobutane system. Part 13. Bromination of bicyclobutanes: a possible case of an electron-transfer mechanism

Drora. Cohen, S. Hoz, M. Livneh, 1987 .

1,3-Diphenylsulphonylcyclobutane: an unprecedented case of a higher stability of the trans isomer of 1,3-disubstituted cyclobutane

S. Cohen, S. Hoz, A. Sella, 1998 .

Bridgehead substituents effect on the reactivity of bicyclobutane in its reactions with nucleophiles. A comparison with olefinic systems

S. Hoz, Carmela Azran, 1995 .

Cyclobutane-Bicyclobutane System. Part 13. Bromination of Bicyclobutanes: A Possible Case of an Electron-Transfer Mechanism.

Drora. Cohen, S. Hoz, M. Livneh, 1987 .

Pyrolytic Reactions of Carbohydrates, Part VIII. The Decomposition of D-Glucose Labelled with 14C at Different Positions, Catalyzed by Various Additives

S. Patai, S. Hoz, Y. Houminer, 1969 .

Bridgehead Substituents Effect on the Reactivity of Bicyclobutane in Its Reactions with Nucleophiles. A Comparison with Olefinic Systems.

S. Hoz, Carmela Azran, 1996 .

Conversion of cyclobutane to bicyclobutane by base-catalyzed 1,3-dehydrohalogenation reaction: a mechanistic study

S. Hoz, M. Livneh, 1987 .

Cyclobutane-bicyclobutane system. 11. Mechanism and stereochemistry of general acid-catalyzed additions to bicyclobutane

Drora. Cohen, S. Hoz, M. Livneh, 1986 .

CYCLOBUTANE-BICYCLOBUTANE SYSTEM. 2. PROTONATION, DEPROTONATION, AND INTERMEDIATE CARBANION STEREOCHEMISTRY IN THE 1,3-HYDROCHLORIC ACID ELIMINATION FROM 3-CHLOROCYCLOBUTANECARBONITRILE

M. Albeck, S. Hoz, M. Livneh, 1979 .

Ligand exchange processes in tetraalkoxytelluranes

H. Gottlieb, M. Albeck, S. Hoz, 1994 .

A very slow ElcB elimination under extreme ElcB conditions

Z. Rappoport, M. Albeck, S. Hoz, 1972 .

Could ionic gamma-elimination be concerted: clocking the internal displacement across a cyclobutane ring.

S. Hoz, Esther Rozental, Uri Habusha, 2002, Journal of the American Chemical Society.

A multi-configurational study of the one-dimensional dissociation of azidopentazole (N8) and derived N7CH isomers

M. Goldberg, H. Basch, S. Hoz, 2003 .

Cyclobutane-bicyclobutane system

R. Levy, S. Hoz, 1985 .

Cyclobutane-bicyclobutane system: Part 10. Conformation and stability of 1-bicyclobutylcarbinyl anion

R. Levy, S. Hoz, 1985 .

Concerted motion in bicyclobutane

H. Basch, S. Hoz, A. Sella, 1998 .

Cyclobutane‐Bicyclobutane System. Part 10. Conformation und Stability of 1‐Bicyclobutylcarbinyl Anion

R. Levy, S. Hoz, 1985 .

Coupling of internal motions in bicyclobutane radical cation: the effect of a positive charge on a radical center

H. Basch, Drora. Cohen, S. Hoz, 1987 .

Relative reactivity of three and four membered rings--the absence of charge effect.

M. Sprecher, H. Basch, S. Hoz, 2004, Organic & biomolecular chemistry.

Quantification of the various contributors to rate enhancement in nucleophilic strain releasing reactions.

H. Basch, T. Hoz, S. Hoz, 2001, Journal of Organic Chemistry.

Reactivity of Strained Compounds: Is Ground State Destabilization the Major Cause for Rate Enhancement?1

H. Basch, S. Hoz, A. Sella, 1996 .

Strain release is not enough

H. Basch, S. Hoz, A. Sella, 1996 .

The Origin of the Auxetic Effect in Prismanes : Bowtie Structure and the Mechanical Properties of Biprismanes

N. Pour, H. Basch, E. Altus, 2009 .

Dissociation of the phenanthroimidazole dimer : A highly delocalized radical - Gomberg revisited

E. Buncel, P. Kazmaier, S. Hoz, 2005 .

Atomic Motions and Protonation Stereochemistry in Nucleophilic Additions to Bicyclobutanes1

S. Hoz, A. Sella, Carmela Azran, 1996 .

Charge transfer complexes between azidopentazole and aromatic nuclei

M. Goldberg, H. Basch, S. Hoz, 2004 .