Home

připojit kulka Monarcha vinylsilane palladium pojem pro mě Dýchání

Recent advances in the application of nano-catalysts for Hiyama  cross-coupling reactions - RSC Advances (RSC Publishing)
Recent advances in the application of nano-catalysts for Hiyama cross-coupling reactions - RSC Advances (RSC Publishing)

Hydroesterification - an overview | ScienceDirect Topics
Hydroesterification - an overview | ScienceDirect Topics

SO 2 conversion to sulfones: development and mechanistic insights of a  sulfonylative Hiyama cross-coupling - Chemical Communications (RSC  Publishing) DOI:10.1039/C9CC06858A
SO 2 conversion to sulfones: development and mechanistic insights of a sulfonylative Hiyama cross-coupling - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC06858A

Palladium-catalyzed sequential three-component reactions to access  vinylsilanes - Chemical Communications (RSC Publishing)
Palladium-catalyzed sequential three-component reactions to access vinylsilanes - Chemical Communications (RSC Publishing)

Pincer cobalt complex-catalyzed Z -selective hydrosilylation of terminal  alkynes - Organic Chemistry Frontiers (RSC Publishing)  DOI:10.1039/C7QO00250E
Pincer cobalt complex-catalyzed Z -selective hydrosilylation of terminal alkynes - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C7QO00250E

PDF) The effect of added silver nitrate on the palladium-catalyzed  arylation of allyltrimethylsilanes
PDF) The effect of added silver nitrate on the palladium-catalyzed arylation of allyltrimethylsilanes

Palladium-catalyzed sequential three-component reactions to access  vinylsilanes - Chemical Communications (RSC Publishing)  DOI:10.1039/C8CC05254A
Palladium-catalyzed sequential three-component reactions to access vinylsilanes - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC05254A

Stereoselective Synthesis of Cis- and Trans-Tetrasubstituted Vinyl Silanes  Using a Silyl-Heck Strategy and Hiyama Conditions for Their Cross-Coupling.  - J. Am. Chem. Soc. - X-MOL
Stereoselective Synthesis of Cis- and Trans-Tetrasubstituted Vinyl Silanes Using a Silyl-Heck Strategy and Hiyama Conditions for Their Cross-Coupling. - J. Am. Chem. Soc. - X-MOL

Solvent interception, heterocyclization and desilylation upon NBS-induced  sulfamidation of trimethyl(vinyl)silane. - Org. Biomol. Chem. - X-MOL
Solvent interception, heterocyclization and desilylation upon NBS-induced sulfamidation of trimethyl(vinyl)silane. - Org. Biomol. Chem. - X-MOL

Inorganics | Free Full-Text | Non-Selective Dimerization of Vinyl Silanes  by the Putative (Phenanthroline)PdMe Cation to  1,4-Bis(trialkoxysilyl)butenes | HTML
Inorganics | Free Full-Text | Non-Selective Dimerization of Vinyl Silanes by the Putative (Phenanthroline)PdMe Cation to 1,4-Bis(trialkoxysilyl)butenes | HTML

Table 1 from Palladium-Catalyzed Ortho-Silylation of Aryl Iodides with  Concomitant Arylsilylation of Oxanorbornadiene: Accessing Functionalized (  Z)-β-Substituted Vinylsilanes and Their Analogues. | Semantic Scholar
Table 1 from Palladium-Catalyzed Ortho-Silylation of Aryl Iodides with Concomitant Arylsilylation of Oxanorbornadiene: Accessing Functionalized ( Z)-β-Substituted Vinylsilanes and Their Analogues. | Semantic Scholar

Copper-catalyzed Hiyama cross-coupling using vinylsilanes and benzylic  electrophiles - Chemical Communications (RSC Publishing)  DOI:10.1039/C4CC02923B
Copper-catalyzed Hiyama cross-coupling using vinylsilanes and benzylic electrophiles - Chemical Communications (RSC Publishing) DOI:10.1039/C4CC02923B

Inorganics | Free Full-Text | Non-Selective Dimerization of Vinyl Silanes  by the Putative (Phenanthroline)PdMe Cation to  1,4-Bis(trialkoxysilyl)butenes | HTML
Inorganics | Free Full-Text | Non-Selective Dimerization of Vinyl Silanes by the Putative (Phenanthroline)PdMe Cation to 1,4-Bis(trialkoxysilyl)butenes | HTML

Palladium-Catalyzed Ortho-Silylation of Aryl Iodides with Concomitant  Arylsilylation of Oxanorbornadiene: Accessing Functionalized  (Z)-β-Substituted Vinylsilanes and Their Analogues - Org. Lett. - X-MOL
Palladium-Catalyzed Ortho-Silylation of Aryl Iodides with Concomitant Arylsilylation of Oxanorbornadiene: Accessing Functionalized (Z)-β-Substituted Vinylsilanes and Their Analogues - Org. Lett. - X-MOL

PdCl2(CH3CN)2-catalyzed regioselective C–H olefinations of 2-amino biaryls  with vinylsilanes as unactivated alkenes - Chemical Communications (RSC  Publishing)
PdCl2(CH3CN)2-catalyzed regioselective C–H olefinations of 2-amino biaryls with vinylsilanes as unactivated alkenes - Chemical Communications (RSC Publishing)

Synthetic Applications of Allylsilanes and Vinylsilanes - Luh - - Major  Reference Works - Wiley Online Library
Synthetic Applications of Allylsilanes and Vinylsilanes - Luh - - Major Reference Works - Wiley Online Library

Synthetic Applications of Allylsilanes and Vinylsilanes - Luh - - Major  Reference Works - Wiley Online Library
Synthetic Applications of Allylsilanes and Vinylsilanes - Luh - - Major Reference Works - Wiley Online Library

Surface functionalization of magnetic nanoparticles via palladium‐catalyzed  Diels‐Alder approach - ChemistrySelect - X-MOL
Surface functionalization of magnetic nanoparticles via palladium‐catalyzed Diels‐Alder approach - ChemistrySelect - X-MOL

Divergent Synthesis of Vinyl‐, Benzyl‐, and Borylsilanes: Aryl to Alkyl 1,5‐ Palladium Migration/Coupling Sequences - Han - 2020 - Angewandte Chemie -  Wiley Online Library
Divergent Synthesis of Vinyl‐, Benzyl‐, and Borylsilanes: Aryl to Alkyl 1,5‐ Palladium Migration/Coupling Sequences - Han - 2020 - Angewandte Chemie - Wiley Online Library

Vinylsilane synthesis
Vinylsilane synthesis

Pd-Catalyzed one-pot synthesis of vinylsilanes via a three-component tandem  reaction - Organic Chemistry Frontiers (RSC Publishing)
Pd-Catalyzed one-pot synthesis of vinylsilanes via a three-component tandem reaction - Organic Chemistry Frontiers (RSC Publishing)

Preparation of Allyl and Vinyl Silanes by the Palladium‐Catalyzed  Silylation of Terminal Olefins: A Silyl‐Heck Reaction - McAtee - 2012 -  Angewandte Chemie - Wiley Online Library
Preparation of Allyl and Vinyl Silanes by the Palladium‐Catalyzed Silylation of Terminal Olefins: A Silyl‐Heck Reaction - McAtee - 2012 - Angewandte Chemie - Wiley Online Library

A Bithiophene‐Promoted ppm Levels of Palladium‐Catalyzed Regioselective  Hydrosilylation of Terminal Allenes - Chen - 2020 - Advanced Synthesis  & Catalysis - Wiley Online Library
A Bithiophene‐Promoted ppm Levels of Palladium‐Catalyzed Regioselective Hydrosilylation of Terminal Allenes - Chen - 2020 - Advanced Synthesis & Catalysis - Wiley Online Library

SO2 conversion to sulfones: development and mechanistic insights of a  sulfonylative Hiyama cross-coupling - Chemical Communications (RSC  Publishing)
SO2 conversion to sulfones: development and mechanistic insights of a sulfonylative Hiyama cross-coupling - Chemical Communications (RSC Publishing)

Selective synthesis of (E)-triethyl(2-arylethenyl)silane derivatives by  reaction of aryl bromides with triethyl vinylsilane catalysed by a palladium–tetraphosphine  complex - ScienceDirect
Selective synthesis of (E)-triethyl(2-arylethenyl)silane derivatives by reaction of aryl bromides with triethyl vinylsilane catalysed by a palladium–tetraphosphine complex - ScienceDirect

sample
sample