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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/12/02 23:48:40」(JST)

English Journal

Chiral-Substituted Poly-N-vinylpyrrolidinones and Bimetallic Nanoclusters in Catalytic Asymmetric Oxidation Reactions.

Hao B1, Gunaratna MJ1, Zhang M1, Weerasekara S1, Seiwald SN1, Nguyen VT1, Meier A1, Hua DH1.
Journal of the American Chemical Society.J Am Chem Soc.2016 Dec 28;138(51):16839-16848. doi: 10.1021/jacs.6b12113. Epub 2016 Dec 15.
A new class of poly-N-vinylpyrrolidinones containing an asymmetric center at C5 of the pyrrolidinone ring were synthesized from l-amino acids. The polymers, particularly 17, were used to stabilize nanoclusters such as Pd/Au for the catalytic asymmetric oxidations of 1,3- and 1,2-cycloalkanediols and
PMID 27976875

Visible-Light Promoted Distereodivergent Intramolecular Oxyamidation of Alkenes.

Ren X1, Guo Q1, Chen J1,2, Xie H3, Xu Q2, Lu Z1.
Chemistry (Weinheim an der Bergstrasse, Germany).Chemistry.2016 Dec 23;22(52):18695-18699. doi: 10.1002/chem.201603977. Epub 2016 Nov 15.
The visible-light-promoted diastereodivergent intramolecular oxyamination of alkenes is described to construct oxazolindinones, pyrrolidinones and imidazolidones via mild generation of primary amidyl radicals from functionalized hydroxylamines. A unique phenomenon of highly diastereoselective ring-o
PMID 27770547

Secondary Amides as Hydrogen Atom Transfer Promoters for Reactions of Samarium Diiodide.

Chciuk TV1, Li AM1, Vazquez-Lopez A1, Anderson WR Jr1, Flowers RA 2nd1.
Organic letters.Org Lett.2016 Dec 21. doi: 10.1021/acs.orglett.6b03664. [Epub ahead of print]
Two secondary amides (N-methylacetamide and 2-pyrrolidinone) were used as additives with SmI2 in THF to estimate the extent of N-H bond weakening upon coordination. Mechanistic and synthetic studies demonstrate significant bond-weakening, providing a reagent system capable of reducing a range of sub
PMID 28001419

SYNTHESIS OF NOVEL BENZIMIDAZOLES 2-FUNCTIONALIZED WITH PYRROLIDINONE AND γ-AMINO ACID WITH A HIGH ANTIBACTERIAL ACTIVITY

Heterocycles : an international journal for reviews and communications in heterocyclic chemistry 92(2), 235-251, 2016-02-01
NAID 40020796956

Total Synthesis of Biologically Active Natural Products Based on Highly Selective Synthetic Methodologies

リンク元	「ピロリジノン」「pyrrolidone」

2-Pyrrolidone
	IUPAC name 2-Pyrrolidone
	Other names 2-Pyrrolidinone
Identifiers
CAS number	616-45-5
ChemSpider	11530
UNII	KKL5D39EOL
ChEBI	CHEBI:36592
ChEMBL	CHEMBL276849
Jmol-3D images	Image 1
	SMILES O=C1NCCC1 ;
	InChI InChI=1S/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6) ; Key: HNJBEVLQSNELDL-UHFFFAOYSA-N InChI=1/C4H7NO/c6-4-2-1-3-5-4/h1-3H2,(H,5,6); Key: HNJBEVLQSNELDL-UHFFFAOYAP ;
Properties
Molecular formula	C4H7NO
Molar mass	85.10 g mol−1
Density	1.116 g/cm³
Melting point	25 °C, 298 K, 77 °F ()
Boiling point	245 °C, 518 K, 473 °F ()
Hazards
MSDS	ScienceLab.com
NFPA 704	1 2 0
Flash point	129 °C (264 °F) (open cup); 138 °C (280 °F) (closed cup)
	(verify) (what is: /?); Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
	Infobox references