New methodology for the introduction of sulfur into organic molecules. Synthesis of anhydrous Li2S, Li2S2 and LiSr species by lithium triethylborohydride reduction of elemental sulfur and disulfides

Tetrahedron

Volumn 35, Issue 20, 1979, Pages 2329-2335

  Gladysz, J A ^a   Wong, Victor K ^a   Jick, Bryan S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000698622     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)93746-9     Document Type: Article

References (50)

1. A Convenient Synthesis of Primary and Secondary Dialkyl and Aryl Alkyl Sulfides in the Presence of Phase-Transfer Catalysts
2. A new Method for the Synthesis of Many-membered Sulfides by Means of Thioacetamide
3. Introduction of sulphur into organic molecules via lithium triethylborohydride reduction of S8
4. Aralkyl hydrodisulfides. X. Reactions with iron salts
5. Organosulphur compounds. Part VIII. Reaction of monothiocarboxylic acids with dicyclohexylcarbodi-imide and other reactions leading to monothio-anhydrides
6. A Convenient Synthesis of Acetyl Sulfide
7. Über unsymmetrische Diacylsulfide und ihre Spaltung mit Chlor oder Brom
8. The Preparation of Acyl Alkoxycarbonyl Sulfides and the Related Compounds
9. Enethiols. VIII. 3-Mercapto-5,5-dimethyl-2-cyclohexen-1-one ("Thiodimedone") and Derivatives. Thermal and Photochemical Rearrangements.
10. Lithium thiomethoxide: A convenient mercaptide reagent