All Stories

  1. Ebselen-like Catalysts – New Approach
  2. Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3(2H)-ones
  3. Electrophilic Selenium Reagents: Addition Reactions to Double Bonds and Selenocyclizations
  4. The Use of Sulfides Derived from Carane, P-Menthane, Pinane, and Bornane in the Synthesis of Optically Active Epoxides
  5. Synthesis and Reactions of New Tellurium-substituted Terpenyl Compounds
  6. Synthesis and reactions of the optically active selenols derived from monoterpenes
  7. Preparation and characterization of new chiral ferrocenyl selenides
  8. ChemInform Abstract: Selenium Compounds with Valency Higher than Two
  9. Selenium Compounds with Valency Higher than Two
  10. ChemInform Abstract: New Chiral Selenium Electrophiles Derived from Functionalized Terpenes.
  11. New chiral selenium electrophiles derived from functionalized terpenes
  12. Syntheses and reactions of terpene β-hydroxyselenides and β-hydroxydiselenides
  13. ChemInform Abstract: Synthesis and Reactions of the Optically Active Dialkyl Diselenides from the Pinane Group.
  14. Syntheses of the Optically Active Terpene Hydroxyphenylselenides
  15. Synthesis of Selenium Derivatives of 3-Hydroxy-2-substituted-2,3-dihydroisoindol-1-ones
  16. Synthesis and Reactions of the Optically Active Dialkyl Diselenides from the Pinane Group
  17. ChemInform Abstract: Asymmetric Selenocyclization with the Use of Dialkyl Monoterpene Diselenides.
  18. Synthesis and reactions of enantiomerically pure dialkyl diselenides from the p-menthane group
  19. Asymmetric selenocyclization with the use of dialkyl monoterpene diselenides
  20. Syntheses and Reactions of Allyl Phenylselenides. A Convenient Method of the Allyl Methylcarbamates Synthesis.
  21. Helicity discrimination in diselenides by chiral substituents—a circular dichroism study
  22. Syntheses and Reactions of New Optically Active Terpene Dialkyl Diselenides
  23. Convenient Route to Dialkyl Diselenides from Alkyl Tosylates. Synthesis of Di(cis‐myrtanyl) Diselenide.
  24. Convenient route to dialkyl diselenides from alkyl tosylates. Synthesis of di(cis-myrtanyl) diselenide
  25. ChemInform Abstract: Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part 17. Reactions of Acyclic and Monocyclic Chlorides with Phenyltelluro‐ and Phenylselenosodium.
  26. ChemInform Abstract: Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part 16. Reactions of (‐)‐4‐Chloro‐3(10)‐carene and (+)‐10‐Chloro‐3‐carene with Phenyltelluro‐ and Phenylselenosodium.
  27. ChemInform Abstract: Reaction of (+)‐3‐Carene and (+)‐2‐Carene with t‐Butyl Hypochlorite or N‐Chlorosuccinimide in the Presence of Free Radical Catalysts.
  28. ChemInform Abstract: Synthesis and Reaction of Organic Compounds with a Nitrogen Atom. Part 15. Reactions of (+)‐3‐Chloro‐2(10)‐pinene and (‐)‐10‐Chloro‐2‐pinene with Phenyltelluro‐ and Phenylselenosodium.
  29. ChemInform Abstract: Reaction of Allylic Alcohols with Aliphatic Alcohols in the Presence of Cerium(III) Chloride. Part 2.
  30. ChemInform Abstract: Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part 13. Reaction of α‐ and β‐Pyronene with Bis(p‐toluenesulfonyl)selenodiimide.
  31. ChemInform Abstract: Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part 12. Toluenesulfonamidation of (+)‐2‐Carene and Synthesis of Amines and Aminoalcohols of the Carene Group
  32. ChemInform Abstract: Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part 10. Synthesis of Allylic 1,2‐Ditoluenesulfonamide, 1,2‐Diamine, Hydroxy‐1,2‐ditoluenesulfonamide and Hydroxy‐1,2‐diamine from (+)‐. alpha.‐Phellandrene.
  33. ChemInform Abstract: Application of Organolithium and Related Reagents in Synthesis. Part 11. Metalation of 2‐Methyl‐ and 4‐Methylnicotinic Acids. A Useful Method for Preparation of Aza‐Isocoumarins.
  34. Application of Organolithium and Related Reagents in Synthesis. Part 111. Metallation of 2-Methyl- and 4-Methylnicotinic Acids. A Useful Method for Preparation of AZA-Isocoumarins