ファッション H.H.C.O 1.0ml 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。

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

Organophotocatalytic selective deuterodehalogenation of aryl or alkyl  chlorides | Nature Communications
Organophotocatalytic selective deuterodehalogenation of aryl or alkyl chlorides | Nature Communications

Asymmetric Syntheses of the Homalium Alkaloids (−)-(S,S)-Homaline and  (−)-(R,R)-Hopromine | The Journal of Organic Chemistry
Asymmetric Syntheses of the Homalium Alkaloids (−)-(S,S)-Homaline and (−)-(R,R)-Hopromine | The Journal of Organic Chemistry

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

Synthesis and Evaluation of CC-1065 and Duocarmycin Analogs Incorporating  the 1,2,3,4,11,11a-Hexahydrocyclopropa[c]naphtho[2,1-b]azepin-6-one (CNA)  Alkylation Subunit: Structural Features that Govern Reactivity and Reaction  Regioselectivity | The ...
Synthesis and Evaluation of CC-1065 and Duocarmycin Analogs Incorporating the 1,2,3,4,11,11a-Hexahydrocyclopropa[c]naphtho[2,1-b]azepin-6-one (CNA) Alkylation Subunit: Structural Features that Govern Reactivity and Reaction Regioselectivity | The ...

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

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

Asymmetric Syntheses of the Homalium Alkaloids (−)-(S,S)-Homaline and  (−)-(R,R)-Hopromine | The Journal of Organic Chemistry
Asymmetric Syntheses of the Homalium Alkaloids (−)-(S,S)-Homaline and (−)-(R,R)-Hopromine | The Journal of Organic Chemistry

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


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

Palladium‐catalyzed Synthesis of Fused Carbo‐ and Heterocycles - Ghosh -  2022 - Chemistry – An Asian Journal - Wiley Online Library
Palladium‐catalyzed Synthesis of Fused Carbo‐ and Heterocycles - Ghosh - 2022 - Chemistry – An Asian Journal - Wiley Online Library

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

Syntheses and Biological Activities of the LMNO, ent-LMNO, and NOPQR(S)  Ring Systems of Maitotoxin | The Journal of Organic Chemistry
Syntheses and Biological Activities of the LMNO, ent-LMNO, and NOPQR(S) Ring Systems of Maitotoxin | The Journal of Organic Chemistry

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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