Shmuel Braverman
Affiliations: | 1963- | Bar- Ilan University |
Area:
Reaction Mechanisms and SynthesisWebsite:
https://ch.biu.ac.il/bravermanGoogle:
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Publications
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Braverman S, Cherkinsky M, Kalendar Y, et al. (2014) Synthesis of water-soluble vinyl selenides and their high glutathione peroxidase (GPx)-like antioxidant activity Synthesis (Germany). 46: 119-125 |
Braverman S, Cherkinsky M, Kalendar Y, et al. (2014) ChemInform Abstract: Synthesis of Water-Soluble Vinyl Selenides and Their High Glutathione Peroxidase (GPx)-Like Antioxidant Activity. Cheminform. 45: no-no |
Braverman S, Cherkinsky M, Kalendar Y, et al. (2013) One-pot three-component preparation of novel selenium-containing spiroketals Journal of Physical Organic Chemistry. 26: 102-108 |
Braverman S, Cherkinsky M, Pechenick-Azizi T, et al. (2011) Chalcogen halides plus propargyl alcohols - Fascinating reaction pathways and products Phosphorus, Sulfur and Silicon and the Related Elements. 186: 1251-1254 |
Braverman S, Pechenick-Azizi T, Gottlieb HE, et al. (2011) Synthesis and reactivity of divinylselenium dichlorides and dibromides Synthesis. 577-584 |
Braverman S, Cherkinsky M, Meridor D, et al. (2010) Synthesis and reactivity of dipropargylic disulfides: tandem rearrangements, cyclization, and oxidative dimerization Tetrahedron. 66: 1925-1930 |
Braverman S, Cherkinsky M, Jana R, et al. (2010) Erratum: Reaction of selenium and tellurium halides with propargyl alcohols. The regio‐ and stereoselectivity of addition to the triple bond, Erratum to poc.1729 Journal of Physical Organic Chemistry. 23: 1121-1121 |
Braverman S, Cherkinsky M, Jana R, et al. (2010) Reaction of selenium and tellurium halides with propargyl alcohols. the regio- and stereoselectivity of addition to the triple bond Journal of Physical Organic Chemistry. 23: 1114-1120 |
Braverman S, Pechenick T, Zafrani Y. (2010) ChemInform Abstract: Facile Synthesis and Rearrangement of Propargylic Trifluoromethanesulfinates. Cheminform. 32: no-no |
Raj CP, Pichnit T, Braverman S. (2010) ChemInform Abstract: Synthesis of Exocyclic cisoid Dienes by Ramberg-Baecklund Rearrangement. Cheminform. 31: no-no |