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לשרוד צוואר ערוץ vinyl triflate retort עינויים מוח

Synthesis of α‐Trifluoromethylated Ketones from Vinyl Triflates in the  Absence of External Trifluoromethyl Sources - Kawamoto - 2017 - Angewandte  Chemie International Edition - Wiley Online Library
Synthesis of α‐Trifluoromethylated Ketones from Vinyl Triflates in the Absence of External Trifluoromethyl Sources - Kawamoto - 2017 - Angewandte Chemie International Edition - Wiley Online Library

Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access  and applications to organic synthesis - ScienceDirect
Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access and applications to organic synthesis - ScienceDirect

Radical Desulfur-Fragmentation and Reconstruction of Enol Triflates: Facile  Access to α-Trifluoromethyl Ketones. | Semantic Scholar
Radical Desulfur-Fragmentation and Reconstruction of Enol Triflates: Facile Access to α-Trifluoromethyl Ketones. | Semantic Scholar

Scheme 9 | A review on various aspects of organic synthesis using Comins'  reagent | SpringerLink
Scheme 9 | A review on various aspects of organic synthesis using Comins' reagent | SpringerLink

Triflates - an overview | ScienceDirect Topics
Triflates - an overview | ScienceDirect Topics

Stille reaction - Wikiwand
Stille reaction - Wikiwand

Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access  and applications to organic synthesis - ScienceDirect
Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access and applications to organic synthesis - ScienceDirect

The Smith Synthesis of (-)-Nodulisporic Acid D
The Smith Synthesis of (-)-Nodulisporic Acid D

PDF) Zinc triflate-mediated cyclopropanation of oxindoles with vinyl  diphenyl sulfonium triflate: a mild reaction with broad functional group  compatibility
PDF) Zinc triflate-mediated cyclopropanation of oxindoles with vinyl diphenyl sulfonium triflate: a mild reaction with broad functional group compatibility

Ni-catalyzed cross-electrophile coupling between vinyl/aryl and alkyl  sulfonates: synthesis of cycloalkenes and modification of peptides -  Chemical Science (RSC Publishing) DOI:10.1039/C9SC03347E
Ni-catalyzed cross-electrophile coupling between vinyl/aryl and alkyl sulfonates: synthesis of cycloalkenes and modification of peptides - Chemical Science (RSC Publishing) DOI:10.1039/C9SC03347E

Tandem one pot asymmetric conjugate addition–vinyl triflate formation–cross  coupling methodology - Organic & Biomolecular Chemistry (RSC Publishing)
Tandem one pot asymmetric conjugate addition–vinyl triflate formation–cross coupling methodology - Organic & Biomolecular Chemistry (RSC Publishing)

Scheme 10 | A review on various aspects of organic synthesis using Comins'  reagent | SpringerLink
Scheme 10 | A review on various aspects of organic synthesis using Comins' reagent | SpringerLink

Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access  and applications to organic synthesis - ScienceDirect
Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access and applications to organic synthesis - ScienceDirect

CAS#:1228046-56-7 | (β-trifluoromethyl)vinyl diphenyl sulfonium triflate |  Chemsrc
CAS#:1228046-56-7 | (β-trifluoromethyl)vinyl diphenyl sulfonium triflate | Chemsrc

Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access  and applications to organic synthesis - ScienceDirect
Vinyl triflates derived from 1,3-dicarbonyl compounds and analogs: access and applications to organic synthesis - ScienceDirect

Computational Organic Chemistry » Authors
Computational Organic Chemistry » Authors

Pd-catalyzed synthesis of α,β-unsaturated ketones by carbonylation of vinyl  triflates and nonaflates - Chemical Communications (RSC Publishing)  DOI:10.1039/C9CC02210D
Pd-catalyzed synthesis of α,β-unsaturated ketones by carbonylation of vinyl triflates and nonaflates - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC02210D

Vinyl triflate | C3H3F3O3S - PubChem
Vinyl triflate | C3H3F3O3S - PubChem

Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and  chlorides. - Abstract - Europe PMC
Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides. - Abstract - Europe PMC

Vinyl Triflate–Aldehyde Reductive Coupling–Redox Isomerization Mediated by  Formate: Rhodium‐Catalyzed Ketone Synthesis in the Absence of  Stoichiometric Metals - Shuler - 2019 - Chemistry – A European Journal -  Wiley Online Library
Vinyl Triflate–Aldehyde Reductive Coupling–Redox Isomerization Mediated by Formate: Rhodium‐Catalyzed Ketone Synthesis in the Absence of Stoichiometric Metals - Shuler - 2019 - Chemistry – A European Journal - Wiley Online Library

In situ acyl triflates ace it | Nature Chemistry
In situ acyl triflates ace it | Nature Chemistry

Nickel-Catalyzed Cross-Electrophile Vinyl–Vinyl Coupling: An Approach to  Structurally Versatile Dienylboronates | CCS Chem
Nickel-Catalyzed Cross-Electrophile Vinyl–Vinyl Coupling: An Approach to Structurally Versatile Dienylboronates | CCS Chem

Vinyl Triflate–Aldehyde Reductive Coupling–Redox Isomerization Mediated by  Formate: Rhodium‐Catalyzed Ketone Synthesis in the Absence of  Stoichiometric Metals - Shuler - 2019 - Chemistry – A European Journal -  Wiley Online Library
Vinyl Triflate–Aldehyde Reductive Coupling–Redox Isomerization Mediated by Formate: Rhodium‐Catalyzed Ketone Synthesis in the Absence of Stoichiometric Metals - Shuler - 2019 - Chemistry – A European Journal - Wiley Online Library

Palladium-catalysed coupling of vinyl triflates with enynes and its  application to the synthesis of 1α,25-dihydroxyvitamin D3 - ScienceDirect
Palladium-catalysed coupling of vinyl triflates with enynes and its application to the synthesis of 1α,25-dihydroxyvitamin D3 - ScienceDirect

EP2428519A2 - Process for the preparation of 17-vinyl- triflates as  intermediates - Google Patents
EP2428519A2 - Process for the preparation of 17-vinyl- triflates as intermediates - Google Patents

SCHEME 3 Z-O-Enecarbamate group as an efficient precursor of Z-vinyl... |  Download Scientific Diagram
SCHEME 3 Z-O-Enecarbamate group as an efficient precursor of Z-vinyl... | Download Scientific Diagram