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Journal articles on the topic '5-menthyloxy-2[5H]-furanone'

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1

de Jong, Johannes C., Fré van Bolhuis, and Ben L. Feringa. "Asymmetric Diels-Alder reactions with 5-menthyloxy-2-(5H)-furanone." Tetrahedron: Asymmetry 2, no. 12 (1991): 1247–62. http://dx.doi.org/10.1016/s0957-4166(00)80024-5.

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2

Rispens, Minze T., Erik Keller, Ben de Lange, Robert W. J. Zijlstra, and Ben L. Feringa. "Asymmetric 1,3-dipolar cycloadditions to 5-(R)-menthyloxy-2(5H)-furanone." Tetrahedron: Asymmetry 5, no. 4 (1994): 607–24. http://dx.doi.org/10.1016/0957-4166(94)80023-5.

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3

Bertrand, Samuel, Norbert Hoffmann, and Jean-Pierre Pete. "Photochemical [2+2] cycloaddition of cyclicenones to(5R)-5-menthyloxy-2[5H]-furanone." Tetrahedron 54, no. 19 (1998): 4873–88. http://dx.doi.org/10.1016/s0040-4020(98)00171-9.

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4

DE JONG, J. C., F. VAN BOLHUIS, and B. L. FERINGA. "ChemInform Abstract: Asymmetric Diels-Alder Reactions with 5-Menthyloxy-2(5H)-furanone." ChemInform 23, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.199217035.

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5

RISPENS, M. T., E. KELLER, B. DE LANGE, R. W. J. ZIJLSTRA, and B. L. FERINGA. "ChemInform Abstract: Asymmetric 1,3-Dipolar Cycloadditions to 5-(R)-Menthyloxy-2(5H)- furanone." ChemInform 25, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199435062.

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6

Aida, Shin, Yasuhiro Nishiyama, Kiyomi Kakiuchi, Norbert Hoffmann, Adeline Fon, and Michael Oelgemoller. "Microflow Photochemistry - Acetone sensitized Addition of Isopropanol to (5R)-5-Menthyloxy-2-(5H)-furanone." Rapid Communication in Photoscience 2, no. 3 (2013): 68–71. http://dx.doi.org/10.5857/rcp.2013.2.3.68.

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7

Lubben, Marcel, та Ben L. Feringa. "Asymmetric synthesis of β-lactams via amine additions to 5(R)-menthyloxy-2[5H]-furanone." Tetrahedron: Asymmetry 2, № 8 (1991): 775–78. http://dx.doi.org/10.1016/s0957-4166(00)80457-7.

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8

Feringa, Ben L., and Johannes C. De Jong. "Asymmetric Diels-Alder reactions with a chiral maleic anhydride analog, 5-(1-menthyloxy)-2(5H)-furanone." Journal of Organic Chemistry 53, no. 5 (1988): 1125–27. http://dx.doi.org/10.1021/jo00240a048.

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9

LUBBEN, M., та B. L. FERINGA. "ChemInform Abstract: Asymmetric Synthesis of β-Lactams via Amine Additions to 5(R)- Menthyloxy-2(5H)-Furanone." ChemInform 22, № 48 (2010): no. http://dx.doi.org/10.1002/chin.199148264.

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10

Fu-An Kang, Zhen-Qiang Yu, Hong-Yi Yin, and Cheng-Lie Yin. "Asymmetric conjugate additions of carbon and oxygen nucleophiles to (R)-(−)-5-[(1R,2S,5R)-menthyloxy]-2(5H)-furanone." Tetrahedron: Asymmetry 8, no. 21 (1997): 3591–96. http://dx.doi.org/10.1016/s0957-4166(97)00479-5.

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11

Hoffmann, Norbert, Hans-Dieter Scharf, and Jan Runsink. "Chiral induction in photochemical reactions-XII. Synthesis of chiral cyclobutane derivatives from (+)-5-menthyloxy-2-[5H]-furanone and ethylene." Tetrahedron Letters 30, no. 20 (1989): 2637–38. http://dx.doi.org/10.1016/s0040-4039(00)99085-3.

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12

Bertrand, Samuel, Cédric Glapski, Norbert Hoffmann, and Jean-Pierre Pete. "Highly efficient photochemical addition of tertiary amines to electron deficient alkenes. Diastereoselective addition to (5R)-5-menthyloxy-2[5H]-furanone." Tetrahedron Letters 40, no. 16 (1999): 3169–72. http://dx.doi.org/10.1016/s0040-4039(99)00451-7.

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13

KANG, F. A., Z. Q. YU, H. Y. YIN, and C. L. YIN. "ChemInform Abstract: Asymmetric Conjugate Additions of Carbon and Oxygen Nucleophiles to (R)-(-)-5-[(1R,2S,5R)-menthyloxy]-2(5H)-furanone." ChemInform 29, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199811045.

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14

QingHua Chen, Zhe Geng, and Bin Huang. "Synthesis of enantiomerically pure 5-(l-menthyloxy)-3,4-dibromo-2(5H)-furanone and its tandem asymmetric Michael addition-elimination reaction." Tetrahedron: Asymmetry 6, no. 2 (1995): 401–4. http://dx.doi.org/10.1016/0957-4166(95)00024-j.

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15

Bertrand, Samuel, Norbert Hoffmann, and Jean-Pierre Pete. "Stereoselective radical addition of tertiary amines to (5R)-5-menthyloxy-2[5H]-furanone: Application to the enantioselective synthesis of (−)-isoretronecanol and (+)-laburnine." Tetrahedron Letters 40, no. 16 (1999): 3173–74. http://dx.doi.org/10.1016/s0040-4039(99)00452-9.

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16

Bertrand, Samuel, Cedric Glapski, Norbert Hoffmann, and Jean-Pierre Pete. "ChemInform Abstract: Highly Efficient Photochemical Addition of Tertiary Amines to Electron-Deficient Alkenes. Diastereoselective Addition to (5R)-5-Menthyloxy-2[5H]-furanone." ChemInform 30, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199929113.

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17

Cong, H. H., R. R. Sibgatullina, A. M. Khabibrakhmanova, A. R. Kurbangalieva, and L. E. Ziganshina. "The possibility of using cell test-systems for screening for anti-inflammatory activity of novel 5(S)-menthyloxy derivatives of 2(5H)-furanone." Kazan medical journal 98, no. 2 (2017): 211–17. http://dx.doi.org/10.17750/kmj2017-211.

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Abstract:
Aim. Study of the possibility of using cell experimental models (erythrocytes hemolysis and platelet aggregation) for screening for anti-inflammatory activity of novel synthesized 5(S)-menthyloxy derivatives of 2(5Н)-furanone (compounds R1-R6). 
 Methods. Evaluation of membrane-stabilizing activity of the test compounds was performed by means of models of erythrocyte hemolysis induced by hypotonic environment (osmotic hemolysis) and free radicals. Antiplatelet effect of the compounds was studied by inducing platelet aggregation by 1 mM arachidonic acid. Study of anti-inflammatory activity
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18

CHEN, Q. H., Z. GENG, and B. HUANG. "ChemInform Abstract: Synthesis of Enantiomerically Pure 5-(l-Menthyloxy)-3,4-dibromo-2(5H)- furanone (III) and Its Tandem Asymmetric Michael Addition-Elimination Reaction." ChemInform 26, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199532139.

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19

Bertrand, Samuel, Norbert Hoffmann, and Jean-Pierre Pete. "ChemInform Abstract: Stereoselective Radical Addition of Tertiary Amines to (5R)-5-Menthyloxy-2[5H]-furanone: Application to the Enantioselective Synthesis of (-)-Isoretronecanol and (+)-Laburnine." ChemInform 30, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199929212.

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20

Fan, Xue-E., Yu-Qin Fu, Jian-Ge Wang, Qiao-Yun Du та Qing-Hua Chen. "A New Synthetic Route to Diastereomerically Pure Cyclopropane-Phosphorus Derivatives Utilizing the Chiron 5-L-Menthyloxy-3-bromo-2(5H)-furanone and Racemic Dialkyl α-Hydroxyalkanephosphonate". Chinese Journal of Chemistry 20, № 11 (2010): 1340–46. http://dx.doi.org/10.1002/cjoc.20020201131.

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21

Sundermann, Bernd, and Hans-Dieter Scharf. "Short and efficient synthesis of enantiomerically pure building blocks for the preparation of carbocyclic nucleosides and prostaglandins via diastereoselective dihydroxylation of 5-menthyloxy-2[5H]-furanone." Tetrahedron: Asymmetry 7, no. 7 (1996): 1995–98. http://dx.doi.org/10.1016/0957-4166(96)00240-6.

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22

SUNDERMANN, B., and H. D. SCHARF. "ChemInform Abstract: Short and Efficient Synthesis of Enantiomerically Pure Building Blocks for the Preparation of Carbocyclic Nucleosides and Prostaglandins via Diastereoselective Dihydroxylation of 5-Menthyloxy-2(5H)-furanone." ChemInform 27, no. 47 (2010): no. http://dx.doi.org/10.1002/chin.199647019.

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23

Kang, Fu-An, Cheng-Lie Yin, and Shi-Wang She. "Synthesis and Characterization of Chiral Nitronic Esters viaO-Alkylation of (4S*,5R)-(+)-4-(1‘-Nitro-1‘-carbethoxymethyl)- 5-[(1R)-menthyloxy]-3,4-dihydro-2(5H)-furanone with Alkyl Halides." Journal of Organic Chemistry 61, no. 16 (1996): 5523–27. http://dx.doi.org/10.1021/jo951902z.

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24

KANG, F. A., C. L. YIN, and S. W. SHE. "ChemInform Abstract: Synthesis and Characterization of Chiral Nitronic Esters via O- Alkylation of (4S*,5R)-(+)-4-(1′-Nitro-1′-carbethoxymethyl)-5-((1R)- menthyloxy)-3,4-dihydro-2(5H)-furanone with Alkyl Halides." ChemInform 28, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199702098.

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25

FERINGA, B. L., and J. C. DE JONG. "ChemInform Abstract: Asymmetric Diels-Alder Reactions with a Chiral Maleic Anhydride Analogue, 5-(1-Menthyloxy)-2(5H)-furanone." ChemInform 19, no. 34 (1988). http://dx.doi.org/10.1002/chin.198834155.

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26

HOFFMANN, N., H. D. SCHARF, and J. RUNSINK. "ChemInform Abstract: Chiral Induction in Photochemical Reactions. Part 12. Synthesis of Chiral Cyclobutane Derivatives from (+)-5-Menthyloxy-2(5H)-furanone (I) and Ethylene (II)." ChemInform 20, no. 52 (1989). http://dx.doi.org/10.1002/chin.198952132.

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