Recent advances in S–S bond formation

B Mandal, B Basu - RSC Advances, 2014 - pubs.rsc.org
Organic compounds possessing S–S bonds, often called disulfides or more specifically
disulfanes, have been widely applied in various fields ranging from biochemistry to different …

Recent developments in disulfide bond formation

D Witt - Synthesis, 2008 - thieme-connect.com
This review summarizes the recent developments of disulfide bond formation with a variety
of reagents. The scope and limitations of the presented methods are discussed. The …

Step‐growth Polymerization of Aziridines with Elemental Sulfur: Easy Access to Linear Polysulfides and Their Use as Recyclable Adhesives

H Huang, S Zheng, J Luo, L Gao, Y Fang… - Angewandte Chemie …, 2024 - Wiley Online Library
The bulk radical polymerization of bis (aziridine) with molten elemental sulfur resulted in
brittle, cross‐linked polymers. However, when the bis (aziridine) was treated with elemental …

Recent developments in the synthesis of unsymmetrical disulfanes (disulfides). A review

M Musiejuk, D Witt - Organic Preparations and Procedures …, 2015 - Taylor & Francis
Compounds with the structure RSSR, where the R group can be alkyl, vinyl or aryl are
termed disulfides and symmetrical disufides when the R groups are the same …

Mild and selective silicon-mediated access to enantioenriched 1, 2-mercaptoamines and β-amino arylchalcogenides

D Tanini, C Borgogni, A Capperucci - New Journal of Chemistry, 2019 - pubs.rsc.org
Metal-free ring opening reactions of activated and unactivated aziridines with different silyl
chalcogenides are described. Judicious tuning of the reaction conditions enables the …

Ring opening of a trisubstituted aziridine with amines: Regio-and stereoselective formation of substituted 1, 2-diamines

BT Kelley, MM Joullie - Organic Letters, 2010 - ACS Publications
The formation of substituted 1, 2-diamines via nucleophilic ring opening of a trisubstituted
ethynyl aziridine was performed with complete regio-and stereoselective control. Various …

A regio-and stereoselective approach to quaternary centers from chiral trisubstituted aziridines

EM Forbeck, CD Evans, JA Gilleran, P Li… - Journal of the …, 2007 - ACS Publications
A thorough investigation of a regio-and stereospecific aziridine ring opening reaction
presents new synthetic technology for the construction of a variety of quaternary β …

Synthesis of unnatural selenocystines and β-aminodiselenides via regioselective ring-opening of sulfamidates using a sequential, one-pot, multistep strategy

NB Rashid Baig, RN Chandrakala… - The Journal of …, 2010 - ACS Publications
A variety of N-alkyl-β-aminodiselenides have been synthesized in high yield from
sulfamidates under mild reaction conditions using potassium selenocyanate and …

Palladium-Catalyzed, Enantioselective Heine Reaction

M Punk, C Merkley, K Kennedy, JB Morgan - ACS catalysis, 2016 - ACS Publications
Aziridines are important synthetic intermediates for the generation of nitrogen-containing
molecules. N-Acylaziridines undergo rearrangement by ring expansion to produce …

Aziridine-based organocatalytic polymerization for tunable sulfur incorporation in polyureas

L Xu, C Ju, J Zheng, Q Chen, Z Zhang - Polymer Chemistry, 2025 - pubs.rsc.org
Developing new methods for converting inorganic sulfur into sulfur-containing polymers is
crucial for advancing both sustainable development and innovative polymeric materials. In …