L-Pipecolinic Acid
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L-Pipecolinic Acid

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L-Pipecolinic Acid is a proline-based organocatalyst that has been investigated for several powerful asymmetric transformations, such as the Aldol, Mannich, and Michael reactions.

Category
Cyclic Amino Acids
Catalog number
BAT-008022
CAS number
3105-95-1
Molecular Formula
C6H11NO2
Molecular Weight
129.16
L-Pipecolinic Acid
IUPAC Name
(2S)-piperidine-2-carboxylic acid
Synonyms
(S)-Piperidine-2-Carboxylic Acid; L(-)-Pipecolinic Acid; H-Hopro-Oh
Appearance
Almost white powder
Purity
≥ 99% (Titration, Dried basis)
Density
1.125 g/cm3
Melting Point
272°C
Boiling Point
265.8°C at 760 mmHg
Storage
Store at RT
Solubility
Soluble in Methanol, Water
InChI
InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1
InChI Key
HXEACLLIILLPRG-YFKPBYRVSA-N
Canonical SMILES
O=C([C@H]1NCCCC1)O
1. L-pipecolinic acid derived lewis base organocatalyst for asymmetric reduction of n-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances.
Zhouyu Wang, Chao Wang, Jian Sun, Li Zhou. Org Biomol Chem. 2013 Feb 7; 11(5): 787-97. DOI: 10.1039/c2ob26772a. PMID: 23223869.
A series of N-formamides derived from pipecolinic acid have been synthesized and tested as Lewis base catalysts for the enantioselective reduction of N-aryl imines by trichlorosilane. Through the investigation of the structure-efficacy relationship between the side amide group and catalytic performance, several highly effective catalysts were discovered. In particular, arylamido-type catalyst 5i and non-arylamido-type catalyst 6c exhibited high reactivity and enantioselectivity, furnishing the reduction of a wide variety of N-aryl imines with high isolated yields (up to 98%) and ee values (up to 96%) under mild conditions. Moreover, these two catalysts complement each other in terms of their tolerances to nonaromatic ketimines and non-methyl ketimines.
2. Xylapeptide a, An antibacterial cyclopentapeptide with an uncommon l-pipecolinic acid moiety from the associated fungus xylaria sp. (gdg-102).
Rui-Yun Yang, Na Zheng, Chang-Lun Shao, Chang-Yun Wang, Wei-Feng Xu, Jun Li, Fei-Hua Yao, Xue-Mei Hou. Sci Rep. 2017 Jul 31; 7(1): 6937. DOI: 10.1038/s41598-017-07331-4. PMID: 28761094.
Two new cyclopentapeptides, xylapeptide A (1) with an uncommon L-pipecolinic acid moiety, and xylapeptide B (2) having a common L-proline residue were identified from an associated fungus Xylaria sp. isolated from the Chinese medicinal plant Sophora tonkinensis. Their planar structures were elucidated by a comprehensive analysis of NMR and MS spectroscopic spectra. The absolute configurations were determined by Marfey's method and single-crystal X-ray diffraction (Cu Kα) analysis. Xylapeptide A (1) is the first example of cyclopentapeptide with L-Pip of terrestrial origin and showed strong antibacterial activity against Bacillus subtilis and B. cereus with MIC value of 12.5 μg/mL.
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