enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    Organosulfur chemistry is the study of the properties and synthesis of organosulfur compounds, which are organic compounds that contain sulfur. [1] They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin. Nature is abound with organosulfur compounds—sulfur is vital for ...

  3. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    In organic chemistry, a sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity R−S−R' as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. [1] A sulfide is similar to an ether except that it contains a sulfur atom in place of the oxygen.

  4. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure R−O−SO − 3. The SO 4 core is a sulfate group and the R group is any organic residue. All organosulfates are formally esters derived from alcohols and sulfuric acid (H 2 SO 4) although many are not prepared in ...

  5. Category:Organosulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Organosulfur...

    Download as PDF; Printable version; ... Pages in category "Organosulfur compounds" ... This list may not reflect recent changes. Organosulfur chemistry; A. S ...

  6. Thiol-ene reaction - Wikipedia

    en.wikipedia.org/wiki/Thiol-ene_reaction

    In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R'). This reaction was first reported in 1905, [1] but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.

  7. Sulfonate - Wikipedia

    en.wikipedia.org/wiki/Sulfonate

    In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.

  8. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    In organosulfur chemistry, a sulfonyl group is either a functional group found primarily in sulfones, or a substituent obtained from a sulfonic acid by the removal of the hydroxyl group, similarly to acyl groups.

  9. Volatile sulfur compounds - Wikipedia

    en.wikipedia.org/?title=Volatile_sulfur...

    Download as PDF; Printable version; ... move to sidebar hide. From Wikipedia, the free encyclopedia. Redirect page. ... Organosulfur chemistry#Basis for odor of ...