• Title/Summary/Keyword: ${\delta}$-Valerolactone

Search Result 6, Processing Time 0.016 seconds

Conversion of Citron (Citrus junos) Peel Oil by Enterobacter agglomerans

  • PARK , YEON-JIN;KIM, IN-CHEOL;BAEK, HYUNG-HEE;BANG, OK-KYUN;CHANG, HAE-CHOON
    • Journal of Microbiology and Biotechnology
    • /
    • v.14 no.6
    • /
    • pp.1275-1279
    • /
    • 2004
  • Citron peel oil was extracted from citron (Citrus funas) fruit by steam distillation, and was used as starting material for microbial conversion to synthesize attractive flavor compounds by using Enterobacter agglomerans 6L. E. agglomerans was isolated from citron peel and was able to metabolize the citron peel oil and grew well ($A_{600}:\;3.0$) on the citron peel oil as the sole carbon source. Multiple terpene metabolites were produced by E. agglomerans 6L on M9 salt media with citron oil vapor. The identified bioconversion products from the citron peel oil included trans-2-decenal, octanol, $\delta$­valerolactone, $\gamma$-valerolactone, cryptone, hydroxycitronellol, cuminol, and $\gamma$-dodecalactone.

An Efficient Synthesis of α-Amino-δ-valerolactones by the Ugi Five-Center Three-Component Reaction

  • Kim, Young-Bae;Park, Soo-Jung;Geum, Gyo-Chang;Jang, Min-Seok;Kang, Soon-Bang;Lee, Duck-Hyung;Kim, You-Seung
    • Bulletin of the Korean Chemical Society
    • /
    • v.23 no.9
    • /
    • pp.1277-1320
    • /
    • 2002
  • A novel approach to ${\alpha}-amino-{\delta}-valerolactone$ derivatives 8 by the intramolecular Ugi five-center three-component reaction (U-5C-3CR) using the multifunctional starting material, L-pentahomoserine 5 is described.

Synthesis and Degradability of Aliphatic Copolyester and Aliphatic Copolyesteramide(2) (지방족 copolyester 및 copolyesteramide의 합성과 분해성(2))

  • Kim, Woo-Sik;Hyun, Seok-Hee;Jeon, Il-Ryon;Kang, Hye-Jung;Lee, Chi-Giu;Kim, Sung-Hwan
    • Applied Chemistry for Engineering
    • /
    • v.7 no.3
    • /
    • pp.481-489
    • /
    • 1996
  • D,L-lactide (2-LA) was copolymerized with ${\beta}$-methyl-${\delta}$-valerolactone (MVL) using tetraphenyltin as a catalyst and the properties of the copolymers were investigated. The composition of the repeating unit of lactic acid in the copolymers was higher than that in the monomer feeds. The composition of the lactic acid unit in the copolymers decreased with increasing copolymerization time. The yield and the molecular weight of the copolymer increased with increasing 2-LA in the feed composition. These results suggest that the reactivity of 2-LA is larger than that of MVL. The number average molecular weight was in the range of 54,000 to 63,000 and the polydispersity index was in the range of 1.7 to 2.1. The copolymers did not show melting point, but glass transition temperature. The degradable tendency of the copolymers with lipase was almost equal to that of L-lactide-MVL copolymer.

  • PDF

Synthesis of Methoxy Poly(ethylene glycol)/Polyesters Diblock Copolymers and Evaluation of Micellar Characterization as Drug Carrier (메톡시 폴리(에틸렌 글리콜)/폴리에스테르 블록공중합체의 합성 및 미셀 특성 비교)

  • Hyun, Hoon;Yang, Jae-Chan;Kim, Moon-Suk;Lee, Hai-Bang;Khang, Gil-Son
    • Polymer(Korea)
    • /
    • v.30 no.6
    • /
    • pp.464-470
    • /
    • 2006
  • Diblock copolymers consisting of methoxy Poly (ethylene glycol) (MPEG) and poly (${\epsilon}-ca$ prolactone) (PCL), poly(${\delta}-valerolactone$) (PVL), poly(L-lactide) (PLLA), or poly(L-lactide-co-glycolide) (PLGA) were prepared to compare the characterization of diblock copolymers as a drug carrier. MPEG-PCL, MPEG-PVL, MPEG-PLLA, and MPEG-PLGA diblock copolymers were synthesized by the ring-opening polymerization of ${\epsilon}$-caprolactone or ${\delta}$-valerolactone in the presence of $HCl{\cdot}Et_2O$ as a monomer activator at room temperature and by the ring-opening polymerization of L-lactide or a mixture of L-lactide and glycolide in the presence of stannous octoate at $130^{\circ}C$, respectively. The synthesized diblock copolymers were characterized with $^1H-NMR$, GPC, DSC, and XRD. The micellar characterization of MPEG-polyester diblock copolymers in an aqueous phase was carried out by using NMR, dynamic light scattering, AFM, and fluorescence techniques. Most micelles exhibited a spherical shape in AFM. Thus, ore confirmed that the micelles formed with MPEG-polyester diblock copolymers have possibility as a potential hydrophobic drug delivery vehicle because a hydrophobic drug could be preferentially distributed in the micelle core.

Development of New Dihydropyran Linker for Solid-Phase Reaction

  • Ryu, Joon-Hyung;Jeong, Jin-Hyun
    • Archives of Pharmacal Research
    • /
    • v.22 no.6
    • /
    • pp.585-591
    • /
    • 1999
  • The linker which plays a role in connecting a polymer with a scaffold has become an important part n solid-phase reaction. To develop a new linker for alcohols and carbohydrates, dihydropyran moiety was selected in this study. New linker, 1-($4^{l},5^{l}$-dihydro-5H-pyranyl)-7-hydroxyheptan-3-one (5) was synthesized via four steps from $\delta$-valerolactone. This can be called as DDHP-linked Wang resin due to double dihy-dropyran rings. To the one pyran ring of new linker 5 was added Wang resin and other alcohols and carbohydrates as scaffolds were then added successfully to the another pyran ring. Carbohydrate and hydroxyl resins were connected via new linker in a 70% loading yield. The detachment of glucose moiety in the presence of PPTS (2 equiv.) in 1:1 n-buteanol/1,2-dichloroethane at $60^{\circ}C$ for 12 h was carried out quantitatively. When certain combinatorial chemical works are carried out using this dihydropyran linker, Wang resin itself can be recovered. Its fact is particularly very important in industry, because recovered resins can be recycled.

  • PDF