Page last updated: 2024-08-18

4-butyrolactone and 3-hydroxybutanal

4-butyrolactone has been researched along with 3-hydroxybutanal in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (30.00)29.6817
2010's6 (60.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Curran, TT; Das Sarma, K; Zhang, J1
Giri, AK; Hajra, S; Hazra, S1
Mahrwald, R; Markert, M; Scheffler, U1
Feng, X; Lin, L; Liu, X; Shi, J; Yang, Y; Zhao, J; Zheng, K1
Han, X; Huang, KW; Kwiatkowski, J; Lu, Y; Luo, J; Wang, H; Xu, LW1
Chaudhary, A; Das, P; Kaur, P; Singh, B1
Berkessel, A; Gröger, H; Hammel, M; Heidlindemann, M; Hummel, W; Mahrwald, R; Scheffler, U1
Li, H; Ma, D; She, X; Xie, X; Xu, D; Zhao, G; Zhong, Z1
Acosta, JAM; Barbosa, LCA; Boukouvalas, J; Muddala, R1
Ji, P; Meng, X; Wang, W; Yu, C; Zhang, Y1

Other Studies

10 other study(ies) available for 4-butyrolactone and 3-hydroxybutanal

ArticleYear
Novel synthons from mucochloric acid: the first use of alpha,beta-dichloro-gamma-butenolides and gamma-butyrolactams for direct vinylogous aldol addition.
    The Journal of organic chemistry, 2007, Apr-27, Volume: 72, Issue:9

    Topics: 4-Butyrolactone; Aldehydes; Chemistry, Organic; Furans

2007
Asymmetric syntheses of (-)-enterolactone and (7'R)-7'-hydroxyenterolactone via organocatalyzed aldol reaction.
    The Journal of organic chemistry, 2009, Oct-16, Volume: 74, Issue:20

    Topics: 4-Butyrolactone; Aldehydes; Catalysis; Lignans; Molecular Structure; Organic Chemicals

2009
Asymmetric histidine-catalyzed cross-aldol reactions of enolizable aldehydes: access to defined configured quaternary stereogenic centers.
    Journal of the American Chemical Society, 2009, Nov-25, Volume: 131, Issue:46

    Topics: 4-Butyrolactone; Aldehydes; Catalysis; Histidine; Pentoses; Stereoisomerism

2009
Asymmetric direct vinylogous aldol reaction of unactivated gamma-butenolide to aldehydes.
    The Journal of organic chemistry, 2010, Aug-06, Volume: 75, Issue:15

    Topics: 4-Butyrolactone; Aldehydes; Chromatography, High Pressure Liquid; Magnetic Resonance Spectroscopy; Spectrometry, Mass, Electrospray Ionization; Spectrophotometry, Ultraviolet; Stereoisomerism

2010
The direct asymmetric vinylogous aldol reaction of furanones with α-ketoesters: access to chiral γ-butenolides and glycerol derivatives.
    Angewandte Chemie (International ed. in English), 2011, Feb-18, Volume: 50, Issue:8

    Topics: 4-Butyrolactone; Aldehydes; Catalysis; Esters; Glycerol; Quinidine; Stereoisomerism; Tryptophan

2011
Naturally occurring limonene to cinnamyl-type gamma-butyrolactone substituted aldol condensation derivatives as antioxidant compounds.
    Natural product communications, 2012, Volume: 7, Issue:9

    Topics: 4-Butyrolactone; Aldehydes; Antioxidants; Cyclohexenes; Limonene; Structure-Activity Relationship; Terpenes

2012
Chemoenzymatic synthesis of vitamin B5-intermediate (R)-pantolactone via combined asymmetric organo- and biocatalysis.
    The Journal of organic chemistry, 2015, Apr-03, Volume: 80, Issue:7

    Topics: 4-Butyrolactone; Alcohol Dehydrogenase; Aldehydes; Biocatalysis; Biotransformation; Catalysis; Histidine; Molecular Structure; Pantothenic Acid; Stereoisomerism

2015
Asymmetric Total Synthesis of (-)-Kravanhin B.
    Chemistry, an Asian journal, 2015, Volume: 10, Issue:12

    Topics: 4-Butyrolactone; Aldehydes; Catalysis; Cyclization; Cyclohexane Monoterpenes; Diterpenes; Monoterpenes; Stereoisomerism

2015
Synthesis of the Marine Myxobacterial Antibiotic Enhygrolide A.
    Journal of natural products, 2017, 07-28, Volume: 80, Issue:7

    Topics: 4-Butyrolactone; Aldehydes; Alkylation; Anti-Bacterial Agents; Benzylidene Compounds; Catalysis; Marine Biology; Molecular Structure; Myxococcales; Stereoisomerism

2017
Construction of Enantioenriched γ,γ-Disubstituted Butenolides Enabled by Chiral Amine and Lewis Acid Cascade Cocatalysis.
    Organic letters, 2021, 10-01, Volume: 23, Issue:19

    Topics: 4-Butyrolactone; Aldehydes; Amines; Catalysis; Cyclization; Molecular Structure; Pyrrolidines; Stereoisomerism

2021