Fmoc-L-cyclopentylglycine

CAS: 220497-61-0

Ref. 3D-FF49124

Produktinformation

• Name: Fmoc-L-cyclopentylglycine
• Synonyme: Fmoc-Gly(cyclopentyl)-OH(S)-2-Cyclopentyl-2-(Fmoc-amino)-acetic acid, (2S)-2-Cyclopentyl-2-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)acetic acid, (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclopentylacetic acid, (S)-2-Cyclopentyl-2-(Fmoc-Amino)-Acetic Acid, (S)-N-Fmoc-2-Amino-2-Cyclopentyl Acetic Acid, (αS)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclopentaneacetic acid, Cyclopentaneacetic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-, Fmoc-Cpg-Oh, Fmoc-Cyclopentyl-Gly-Oh, Fmoc-Cyclopentyl-Glycine, Fmoc-L-Cyclopentylglycine, N-Alpha-(9-Fluorenylmethoxycarbonyl)-L-Cyclopentylglycine, N-Alpha-(9-Fluorenylmethyloxycarbonyl)-L-Beta-Cyclopentylglycine, N-Alpha-(9-Fluorenylmethyloxycarbonyl)-L-Cyclopentylglycine

Beschreibung

Fmoc-L-cyclopentylglycine is an asymmetric synthesis catalyst that allows the construction of a cyclopentyl ring system. It is synthesized by alkylating a glycine with cyclopentyl bromide, catalytic hydrogenolysis, and high yield. The stereoselectivity of this reaction can be controlled to produce either a syn or anti product. Fmoc-L-cyclopentylglycine has been used in efficient diastereoselective hydrogenolysis of benzyl ethers. The Fmoc group is removed by strong acid (e.g., fmoc-osu) in order to avoid racemization.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 365.42 g/mol
• Formel: C₂₂H₂₃NO₄
• Reinheit: Min. 95%
• Farbe/Form: White Powder