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pro vyhledávání: '"Rachel Ta-Shma"'
Autor:
Eli Breuer, Morris Srebnik, Mordechai Chevion, Avital Torres, Rachel Ta-Shma, Claes D. Enk, Abed Al Aziz Quntar
Publikováno v:
Tetrahedron. 62:5469-5473
Three pyrimidine derivatives (8a–c), differing from isouramil and divicine at C2, have been synthesized and their autoxidation rates measured spectrophotometrically. The autoxidation rates of all five pyrimidines (8a–c, isouramil and divicine) we
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1961-1968
The thermodynamics, pH dependency and solvent effects of the fragmentation reaction of a series of α-oxyiminobenzylphosphonate monomethyl esters [(E)-1a–f] were examined in water and other hydroxylic solvents by UV and by 31P NMR spectroscopy at p
Autor:
Rachel Ta-Shma, Zvi Rappoport
Publikováno v:
ChemInform. 24
Publisher Summary This chapter deals with the selectivity of an electrophilic carbon centre carrying a nucleofuge (RX) or of a solvolytically generated carbocation species (R + ) toward the two nucleophilic solvent components. The chapter explains th
Formation of diethyl 2-amino-1-cyclopentenylphosphonates: a simple synthesis with a unique mechanism
Autor:
Rachel Ta-Shma, Avital Shurki, Morris Srebnik, Artem Melman, Hemant Kumar Srivastava, Abed Al Aziz Quntar
Publikováno v:
The Journal of organic chemistry. 72(13)
Reaction of diethyl 5-chloro-1-pentynylphosphonate with primary and secondary amines produces novel 2-amino-1-cyclopentenylphosphonates, 1, in excellent isolated yields (79−88%). Calculations supported by experimental facts point to a two-step mech
Publikováno v:
ChemInform. 31
The thermodynamics, pH dependency and solvent effects of the fragmentation reaction of a series of α-oxyiminobenzylphosphonate monomethyl esters [(E)-1a–f] were examined in water and other hydroxylic solvents by UV and by 31P NMR spectroscopy at p
Autor:
Rachel Ta-Shma, Zvi Rappoport
Publisher Summary This chapter deals with the selectivity of an electrophilic carbon centre carrying a nucleofuge (RX) or of a solvolytically generated carbocation species (R + ) toward the two nucleophilic solvent components. The chapter explains th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6eae321506ba7dbcbdc772d6a9493c5
https://doi.org/10.1016/s0065-3160(08)60066-0
https://doi.org/10.1016/s0065-3160(08)60066-0
Autor:
William P. Jencks, Rachel Ta-Shma
Publikováno v:
Journal of the American Chemical Society. 108:8040-8050
Structure-reactivity correlations are reported for general base catalysis of the addition of alcohols to 1-(4-(dimethylamino)phenyl)ethyl and 1-(4-methoxyphenyl)ethyl carbocations in 50:40:10 H/sub 2/O: CF/sub 3/CH/sub 2/OH:ROH. The addition of trifl
Autor:
Rachel Ta-Shma, Zvi Rappoport
Publikováno v:
Journal of the American Chemical Society. 105:6082-6095
La linearite suggeree entre les logarithmes de la constante de vitesse de solvolyse de RX et la selectivite dans la capture du cation intermediaire R + par l'eau et l'azote dans l'acetone 80% sont reetudiees en utilisant des donnees de la litterature
Autor:
Zvi Rappoport, Rachel Ta-Shma
Publikováno v:
Tetrahedron Letters. 23:781-784
In contrast to previous reports, the selectivities of four carbenium ions R + towards N 3 − and H 2 O (log(K N 3 − /K H 2 O )) change more than the solvolytic reactivities (log K solv ) of their rather reactive precursors RCl.
Autor:
Rachel Ta-Shma, Zvi Rappoport
Publikováno v:
Journal of the American Chemical Society. 98:8460-8467