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Transition-metal-catalyzed C− S, C− Se, and C− Te bond formation via cross-coupling and atom-economic addition reactions
IP Beletskaya, VP Ananikov - Chemical reviews, 2011 - ACS Publications
Transition metal catalysis has dramatically changed the face of modern organic chemistry by
introducing a range of novel synthetic methods. A number of outstanding catalytic systems …
introducing a range of novel synthetic methods. A number of outstanding catalytic systems …
The emergence of transition‐metal‐mediated hydrothiolation of unsaturated carbon–carbon bonds: a mechanistic outlook
The hydrothiolation of unsaturated carbon–carbon bonds is a practical and atom‐
economical approach for the incorporation of sulfur into organic frameworks. In recent years …
economical approach for the incorporation of sulfur into organic frameworks. In recent years …
Nickel/Lewis acid-catalyzed cyanoesterification and cyanocarbamoylation of alkynes
Y Hirata, A Yada, E Morita, Y Nakao… - Journal of the …, 2010 - ACS Publications
Cyanoformates and cyanoformamides are found to add across alkynes by nickel/Lewis acid
(LA) cooperative catalysis to give β-cyano-substituted acrylates and acrylamides …
(LA) cooperative catalysis to give β-cyano-substituted acrylates and acrylamides …
Aryl methyl sulfides as substrates for rhodium-catalyzed alkyne carbothiolation: arene functionalization with activating group recycling
A Rh (I)-catalyzed method for the efficient functionalization of arenes is reported. Aryl methyl
sulfides are combined with terminal alkynes to deliver products of carbothiolation. The …
sulfides are combined with terminal alkynes to deliver products of carbothiolation. The …
Organometallic approaches to carbon–sulfur bond formation
P Bichler, JA Love - CX Bond Formation, 2010 - Springer
The transition metal mediated synthesis of carbon–sulfur (C–S) bonds is possible with a
variety of simple and tailored metal complexes. This chapter serves to illustrate …
variety of simple and tailored metal complexes. This chapter serves to illustrate …
Two distinct mechanisms of alkyne insertion into the metal–sulfur bond: combined experimental and theoretical study and application in catalysis
The present study reports the evidence for the multiple carbon–carbon bond insertion into
the metal–heteroatom bond via a five‐coordinate metal complex. Detailed analysis of the …
the metal–heteroatom bond via a five‐coordinate metal complex. Detailed analysis of the …
Palladium‐Catalyzed Regio‐and Stereoselective Chlorothiolation of Terminal Alkynes with Sulfenyl Chlorides
M Iwasaki, T Fujii, A Yamamoto… - Chemistry–An Asian …, 2014 - Wiley Online Library
Chlorothiolation of terminal alkynes with sulfenyl chlorides yields anti‐adducts without
transition‐metal catalysts. In sharp contrast, transition‐metal‐catalyzed chlorothiolation has …
transition‐metal catalysts. In sharp contrast, transition‐metal‐catalyzed chlorothiolation has …
Transition-metal-catalyzed S–H and Se–H bonds addition to unsaturated molecules
A Ogawa - Hydrofunctionalization, 2011 - Springer
This chapter deals with the transition-metal-catalyzed hydrothiolation and hydroselenation of
alkynes and allenes and related unsaturated compounds with thiols and selenols. In these …
alkynes and allenes and related unsaturated compounds with thiols and selenols. In these …
Catalytic synthesis of sulfur and phosphorus compounds via atom-economic reactions
S Kawaguchi, Y Yamamoto, A Ogawa - Mendeleev Communications, 2020 - Elsevier
This mini-review focuses on addition reactions, as atomeconomic reactions, employed for
the preparation of organosulfur and organophosphorus compounds. For synthesis of …
the preparation of organosulfur and organophosphorus compounds. For synthesis of …
Nickel-catalysed synthesis of tetrasubstituted vinyl sulfides from thiocarbamates and internal alkynes
T Inami, T Kurahashi, S Matsubara - Chemical Communications, 2015 - pubs.rsc.org
Nickel-catalysed synthesis of tetrasubstituted vinyl sulfides from thiocarbamates and internal
alkynes - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC09123J Royal Society …
alkynes - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC09123J Royal Society …