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9-Fluorenylmethyl chloroformate | C15H11ClO2 - PubChem
9-Fluorenylmethyl chloroformate | C15H11ClO2 - PubChem

The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc)  Amino-Protecting Group | The Journal of Organic Chemistry
The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Amino-Protecting Group | The Journal of Organic Chemistry

9-Fluorenylmethyl Pentafluorophenyl Carbonate 3B-F0936
9-Fluorenylmethyl Pentafluorophenyl Carbonate 3B-F0936

Microwave Assisted Alcoholysis of Isocyanates Derived from N -[(9- fluorenylmethyl)oxy]carbonyl Amino Acids: Synthesis of N-Fmoc-
Microwave Assisted Alcoholysis of Isocyanates Derived from N -[(9- fluorenylmethyl)oxy]carbonyl Amino Acids: Synthesis of N-Fmoc-

Fmoc chloride - 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl  chloroformate
Fmoc chloride - 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate

Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as  Crypto-Peptide Thioester Precursor with Application to Native Chemical  Ligation | The Journal of Organic Chemistry
Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as Crypto-Peptide Thioester Precursor with Application to Native Chemical Ligation | The Journal of Organic Chemistry

Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as  Crypto-Peptide Thioester Precursor with Application to Native Chemical  Ligation | The Journal of Organic Chemistry
Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as Crypto-Peptide Thioester Precursor with Application to Native Chemical Ligation | The Journal of Organic Chemistry

EP0410263B1 - Cationic photoinitiated polymerisation process and the  preparation of relief motifs or photoimages using sulfonium salts - Google  Patents
EP0410263B1 - Cationic photoinitiated polymerisation process and the preparation of relief motifs or photoimages using sulfonium salts - Google Patents

Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis,  characterization, and application to the rapid synthesis of short peptide  segments | The Journal of Organic Chemistry
Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis, characterization, and application to the rapid synthesis of short peptide segments | The Journal of Organic Chemistry

148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic  acid| Ambeed
148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic acid| Ambeed

PDF) Isocyanates of N α -[(9-Fluorenylmethyl)oxy]carbonyl Amino Acids:  Synthesis, Isolation, Characterization, and Application to the Efficient  Synthesis of Urea Peptidomimetics | Vasanthakumar Ganga Ramu - Academia.edu
PDF) Isocyanates of N α -[(9-Fluorenylmethyl)oxy]carbonyl Amino Acids: Synthesis, Isolation, Characterization, and Application to the Efficient Synthesis of Urea Peptidomimetics | Vasanthakumar Ganga Ramu - Academia.edu

9-Fluorenylmethyl)oxy]carbonyl (FMOC) amino acid fluorides. Convienient new  peptide coupling reagents applicable to the FMOC/tert-butyl strategy for  solution and solid-phase syntheses. | Journal of the American Chemical  Society
9-Fluorenylmethyl)oxy]carbonyl (FMOC) amino acid fluorides. Convienient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid-phase syntheses. | Journal of the American Chemical Society

148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic  acid| Ambeed
148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic acid| Ambeed

Extended Diethylglycine Homopeptides Formed by Desulfurization of Their  Tetrahydrothiopyran Analogues | Organic Letters
Extended Diethylglycine Homopeptides Formed by Desulfurization of Their Tetrahydrothiopyran Analogues | Organic Letters

The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc)  Amino-Protecting Group | The Journal of Organic Chemistry
The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Amino-Protecting Group | The Journal of Organic Chemistry

Fmoc chloride - 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl  chloroformate
Fmoc chloride - 9-Fluorenylmethoxycarbonyl chloride, 9-Fluorenylmethyl chloroformate

Fluorenylmethyloxycarbonyl chloride - Wikipedia
Fluorenylmethyloxycarbonyl chloride - Wikipedia

Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as  Crypto-Peptide Thioester Precursor with Application to Native Chemical  Ligation | The Journal of Organic Chemistry
Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as Crypto-Peptide Thioester Precursor with Application to Native Chemical Ligation | The Journal of Organic Chemistry

Factor IX Zutphen: a Cys18-->Arg mutation results in formation of a  heterodimer with alpha 1-microglobulin and the inability to form a  calcium-induced conformation. - Abstract - Europe PMC
Factor IX Zutphen: a Cys18-->Arg mutation results in formation of a heterodimer with alpha 1-microglobulin and the inability to form a calcium-induced conformation. - Abstract - Europe PMC

Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as  Crypto-Peptide Thioester Precursor with Application to Native Chemical  Ligation | The Journal of Organic Chemistry
Synthetic Procedure for N-Fmoc Amino Acyl-N-Sulfanylethylaniline Linker as Crypto-Peptide Thioester Precursor with Application to Native Chemical Ligation | The Journal of Organic Chemistry

9-Fluorenylmethyl chloroformate | C15H11ClO2 - PubChem
9-Fluorenylmethyl chloroformate | C15H11ClO2 - PubChem

148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic  acid| Ambeed
148983-03-3|(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-cyclohexylpropanoic acid| Ambeed

Design and Molecular dynamic Investigations of 7,8-Dihydroxyflavone  Derivatives as Potential Neuroprotective Agents Against Alpha-synuclein |  Scientific Reports
Design and Molecular dynamic Investigations of 7,8-Dihydroxyflavone Derivatives as Potential Neuroprotective Agents Against Alpha-synuclein | Scientific Reports

Use of Phthaloyl Protecting Group for the Automated Synthesis of  3'-[(Hydroxypropyl)amino] and 3'-[(Hydroxypropyltriglyc
Use of Phthaloyl Protecting Group for the Automated Synthesis of 3'-[(Hydroxypropyl)amino] and 3'-[(Hydroxypropyltriglyc

Synthesis and Evaluation of Tryprostatin B and Demethoxyfumitremorgin C  Analogues | Journal of Medicinal Chemistry
Synthesis and Evaluation of Tryprostatin B and Demethoxyfumitremorgin C Analogues | Journal of Medicinal Chemistry