TY - JOUR
T1 - Unilateral and Bilateral Disulfurating Reagents for the Synthesis of Unsymmetrical Polysulfides
AU - Yu, Qing
AU - Jiang, Xuefeng
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/3/17
Y1 - 2025/3/17
N2 - Polysulfides play an essential role across various fields, including life sciences, pharmaceuticals, food science, and materials science. However, the controlled sequential installation of groups at both ends of an S−S motif poses enormous challenges due to the reversible nature of the covalent S−S bond. Utilizing unique disulfide reagents presents one of the most straightforward approaches for constructing diverse polysulfides. This concept highlights the initiatives and advancements in polysulfide synthesis facilitated by unilateral or bilateral disulfide reagents. Furthermore, ongoing research is focused on recently reported methodologies for synthesizing unsymmetrical disulfides.
AB - Polysulfides play an essential role across various fields, including life sciences, pharmaceuticals, food science, and materials science. However, the controlled sequential installation of groups at both ends of an S−S motif poses enormous challenges due to the reversible nature of the covalent S−S bond. Utilizing unique disulfide reagents presents one of the most straightforward approaches for constructing diverse polysulfides. This concept highlights the initiatives and advancements in polysulfide synthesis facilitated by unilateral or bilateral disulfide reagents. Furthermore, ongoing research is focused on recently reported methodologies for synthesizing unsymmetrical disulfides.
KW - bilateral disulfurating reagents
KW - coupling
KW - disulfuration
KW - unilateral disulfurating reagents
KW - unsymmetrical disulfides
UR - https://www.scopus.com/pages/publications/105001086470
U2 - 10.1002/chem.202404029
DO - 10.1002/chem.202404029
M3 - 文章
C2 - 39821407
AN - SCOPUS:105001086470
SN - 0947-6539
VL - 31
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 16
M1 - e202404029
ER -