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 …

New design of a disulfurating reagent: facile and straightforward pathway to unsymmetrical disulfanes by copper‐catalyzed oxidative cross‐coupling

X Xiao, M Feng, X Jiang - Angewandte Chemie International …, 2016 - Wiley Online Library
A novel reagent, which introduces two sulfur atoms in one step, was designed and used for
the construction of diverse disulfanes by copper‐catalyzed oxidative cross‐coupling under …

[PDF][PDF] Rewiring chemistry: algorithmic discovery and experimental validation of one‐pot reactions in the network of organic chemistry

CM Gothard, S Soh, NA Gothard, B Kowalczyk… - Angewandte Chemie …, 2012 - fennetic.net
In 2005 and 2006, we published the first reports [1a, b] on the representation of all synthetic
knowledge as a giant network in which molecule “nodes” are connected by reaction …

Catalytic (3+ 2) umpolung annulations of α-thioacyl carbenes with aryl isothiocyanates

Z Dong, MY Ma, J Xu, Z Yang - Chemical Communications, 2022 - pubs.rsc.org
1, 2, 3-Thiadiazoles serve as masked S-electrophilic thia-1, 3-dipoles. Under
rhodium/racemic BINAP catalysis, they undergo denitrogenative (3+ 2) umpolung …

Nucleophilic disulfurating reagents for unsymmetrical disulfides construction via copper-catalyzed oxidative cross coupling

Z Dai, X Xiao, X Jiang - Tetrahedron, 2017 - Elsevier
Novel disulfuration was established via cross coupling between nucleophilic disulfurating
reagent and arylsilane introducing two sulfur atoms in one step. This methodology was …

Domino Ring-Opening/Carboxamidation Reactions of N-Tosyl Aziridines and 2-Halophenols/Pyridinol: Efficient Synthesis of 1,4-Benzo- and Pyrido-oxazepinones

G Chouhan, H Alper - Organic Letters, 2010 - ACS Publications
Domino Ring-Opening/Carboxamidation Reactions of N-Tosyl Aziridines and 2-Halophenols/Pyridinol:
Efficient Synthesis of 1,4-Benzo- and Pyrido-oxazepinones | Organic Letters ACS ACS …

Synthesis of 1,4‐Benzoxazepine Derivatives via a Novel Domino Aziridine Ring‐Opening and Isocyanide‐Insertion Reaction

F Ji, M Lv, W Yi, C Cai - Advanced Synthesis & Catalysis, 2013 - Wiley Online Library
A novel and efficient domino process has been developed for the synthesis of 1, 4‐
benzoxazepine derivatives from a range of readily accessible N‐tosylaziridines, 2 …

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 …

A facile noncatalytic pathway for the nitrene transfer process: expeditious access to aziridines

I Saikia, B Kashyap, P Phukan - Chemical Communications, 2011 - pubs.rsc.org
A fast and efficient method has been developed for generation of sulfonyl nitrene from N, N-
dibromo-p-toluenesulfonamide (TsNBr2) in the presence of a base without any catalyst. This …

Tandem Ring-Opening/Closing Reactions of N-Ts Aziridines and Aryl Propargyl Alcohols Promoted by t-BuOK

L Wang, QB Liu, DS Wang, X Li, XW Han… - Organic …, 2009 - ACS Publications
Tandem Ring-Opening/Closing Reactions of N-Ts Aziridines and Aryl Propargyl Alcohols
Promoted by t-BuOK | Organic Letters ACS ACS Publications C&EN CAS Find my institution Log …