H.H.C.O 1.0ml 注文 94%

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入荷致しました。 手押し中です! Fruity Pebbles ・1.0ml 94% ※フルーティーな味わいでとても吸いやすいです。

Ni-Catalyzed Enantioconvergent Coupling of Epoxides with Alkenylboronic  Acids: Construction of Oxindoles Bearing Quaternary Carbons | CCS Chemistry
Ni-Catalyzed Enantioconvergent Coupling of Epoxides with Alkenylboronic Acids: Construction of Oxindoles Bearing Quaternary Carbons | CCS Chemistry

Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically  labelled CO2 | Nature Chemistry
Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically labelled CO2 | Nature Chemistry

Asymmetric hydrogenation of 1,1-diarylethylenes and benzophenones through a  relay strategy | Nature Communications
Asymmetric hydrogenation of 1,1-diarylethylenes and benzophenones through a relay strategy | Nature Communications

Copper-catalyzed regioselective C2–H chlorination of indoles with para  -toluenesulfonyl chloride - Organic & Biomolecular Chemistry (RSC  Publishing) DOI:10.1039/D2OB00758D
Copper-catalyzed regioselective C2–H chlorination of indoles with para -toluenesulfonyl chloride - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D2OB00758D

A squaramide-catalysed asymmetric cascade Michael addition/acyl transfer  reaction between unsaturated benzothiophenones and α-nitroketones - Organic  & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB02217B
A squaramide-catalysed asymmetric cascade Michael addition/acyl transfer reaction between unsaturated benzothiophenones and α-nitroketones - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB02217B

Fabrication of pollution-free coal gangue-based catalytic material  utilizing ferrous chloride as activator for efficient peroxymonosulfate  activation | International Journal of Coal Science & Technology
Fabrication of pollution-free coal gangue-based catalytic material utilizing ferrous chloride as activator for efficient peroxymonosulfate activation | International Journal of Coal Science & Technology

Dynamic Kinetic Resolution Based Asymmetric Transfer Hydrogenation of  α-Alkoxy-β-Ketophosphonates. Diastereo- and Enantioselective Synthesis of  Monoprotected 1,2-Dihydroxyphosphonates | The Journal of Organic Chemistry
Dynamic Kinetic Resolution Based Asymmetric Transfer Hydrogenation of α-Alkoxy-β-Ketophosphonates. Diastereo- and Enantioselective Synthesis of Monoprotected 1,2-Dihydroxyphosphonates | The Journal of Organic Chemistry

Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically  labelled CO2 | Nature Chemistry
Aldehyde-catalysed carboxylate exchange in α-amino acids with isotopically labelled CO2 | Nature Chemistry

Sulfanilic Acid - an overview | ScienceDirect Topics
Sulfanilic Acid - an overview | ScienceDirect Topics

Palladium‐Catalyzed Synthesis of N‐Cyclohexyl Anilines from Phenols with  Hydrazine or Hydroxylamine via N‐N/O Cleavage - Li - 2017 - Advanced  Synthesis & Catalysis - Wiley Online Library
Palladium‐Catalyzed Synthesis of N‐Cyclohexyl Anilines from Phenols with Hydrazine or Hydroxylamine via N‐N/O Cleavage - Li - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library

Metabolomic Fingerprinting in the Comprehensive Study of Liver Changes  Associated with Onion Supplementation in Hypercholesterolemic Wistar Rats
Metabolomic Fingerprinting in the Comprehensive Study of Liver Changes Associated with Onion Supplementation in Hypercholesterolemic Wistar Rats

On the Use of Triarylsilanols as Catalysts for Direct Amidation of  Carboxylic Acids - ScienceDirect
On the Use of Triarylsilanols as Catalysts for Direct Amidation of Carboxylic Acids - ScienceDirect

Asymmetric formal sp2-hydrocarbonations of dienes and alkynes via palladium  hydride catalysis | Nature Communications
Asymmetric formal sp2-hydrocarbonations of dienes and alkynes via palladium hydride catalysis | Nature Communications

Photoredox-catalyzed indirect acyl radical generation from thioesters -  Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C8QO00867A
Photoredox-catalyzed indirect acyl radical generation from thioesters - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C8QO00867A

Asymmetric Reduction of Electron-Rich Ketones with Tethered Ru(II)/TsDPEN  Catalysts Using Formic Acid/Triethylamine or Aqueous Sodium Formate -  ScienceDirect
Asymmetric Reduction of Electron-Rich Ketones with Tethered Ru(II)/TsDPEN Catalysts Using Formic Acid/Triethylamine or Aqueous Sodium Formate - ScienceDirect

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