Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes
A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild c...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Li, Na [verfasserIn] Tu, Liang [verfasserIn] Cheng, Guiguang [verfasserIn] Sa, Houling [verfasserIn] Li, Zhenghui [verfasserIn] Feng, Tao [verfasserIn] Zheng, Yongsheng [verfasserIn] Liu, Jikai [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Tetrahedron letters - Amsterdam [u.a.] : Elsevier Science, 1959, 61 |
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| Übergeordnetes Werk: |
volume:61 |
| DOI / URN: |
10.1016/j.tetlet.2019.151579 |
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| Katalog-ID: |
ELV003665372 |
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| 245 | 1 | 0 | |a Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes |
| 264 | 1 | |c 2020 | |
| 336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
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| 520 | |a A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). | ||
| 650 | 4 | |a β-Naphthols | |
| 650 | 4 | |a [3+3] Cycloaddition | |
| 650 | 4 | |a Pentacyclic chromanes | |
| 650 | 4 | |a Immunosuppressant | |
| 700 | 1 | |a Tu, Liang |e verfasserin |4 aut | |
| 700 | 1 | |a Cheng, Guiguang |e verfasserin |4 aut | |
| 700 | 1 | |a Sa, Houling |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Zhenghui |e verfasserin |4 aut | |
| 700 | 1 | |a Feng, Tao |e verfasserin |0 (orcid)0000-0002-1977-9857 |4 aut | |
| 700 | 1 | |a Zheng, Yongsheng |e verfasserin |0 (orcid)0000-0002-1019-5521 |4 aut | |
| 700 | 1 | |a Liu, Jikai |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Tetrahedron letters |d Amsterdam [u.a.] : Elsevier Science, 1959 |g 61 |h Online-Ressource |w (DE-627)320459489 |w (DE-600)2007074-3 |w (DE-576)094107939 |x 1873-3581 |7 nnns |
| 773 | 1 | 8 | |g volume:61 |
| 912 | |a GBV_USEFLAG_U | ||
| 912 | |a SYSFLAG_U | ||
| 912 | |a GBV_ELV | ||
| 912 | |a SSG-OLC-PHA | ||
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| 912 | |a GBV_ILN_32 | ||
| 912 | |a GBV_ILN_40 | ||
| 912 | |a GBV_ILN_60 | ||
| 912 | |a GBV_ILN_62 | ||
| 912 | |a GBV_ILN_63 | ||
| 912 | |a GBV_ILN_65 | ||
| 912 | |a GBV_ILN_69 | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_73 | ||
| 912 | |a GBV_ILN_74 | ||
| 912 | |a GBV_ILN_90 | ||
| 912 | |a GBV_ILN_95 | ||
| 912 | |a GBV_ILN_100 | ||
| 912 | |a GBV_ILN_101 | ||
| 912 | |a GBV_ILN_105 | ||
| 912 | |a GBV_ILN_110 | ||
| 912 | |a GBV_ILN_150 | ||
| 912 | |a GBV_ILN_151 | ||
| 912 | |a GBV_ILN_224 | ||
| 912 | |a GBV_ILN_370 | ||
| 912 | |a GBV_ILN_602 | ||
| 912 | |a GBV_ILN_702 | ||
| 912 | |a GBV_ILN_2003 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_2005 | ||
| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
| 912 | |a GBV_ILN_2015 | ||
| 912 | |a GBV_ILN_2020 | ||
| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_2025 | ||
| 912 | |a GBV_ILN_2027 | ||
| 912 | |a GBV_ILN_2034 | ||
| 912 | |a GBV_ILN_2038 | ||
| 912 | |a GBV_ILN_2044 | ||
| 912 | |a GBV_ILN_2048 | ||
| 912 | |a GBV_ILN_2049 | ||
| 912 | |a GBV_ILN_2050 | ||
| 912 | |a GBV_ILN_2056 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2147 | ||
| 912 | |a GBV_ILN_2148 | ||
| 912 | |a GBV_ILN_2152 | ||
| 912 | |a GBV_ILN_2153 | ||
| 912 | |a GBV_ILN_2190 | ||
| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2507 | ||
| 912 | |a GBV_ILN_2522 | ||
| 912 | |a GBV_ILN_4035 | ||
| 912 | |a GBV_ILN_4037 | ||
| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
| 912 | |a GBV_ILN_4242 | ||
| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4324 | ||
| 912 | |a GBV_ILN_4325 | ||
| 912 | |a GBV_ILN_4326 | ||
| 912 | |a GBV_ILN_4333 | ||
| 912 | |a GBV_ILN_4334 | ||
| 912 | |a GBV_ILN_4335 | ||
| 912 | |a GBV_ILN_4338 | ||
| 912 | |a GBV_ILN_4393 | ||
| 936 | b | k | |a 35.00 |j Chemie: Allgemeines |
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10.1016/j.tetlet.2019.151579 doi (DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Li, Na verfasserin aut Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). β-Naphthols [3+3] Cycloaddition Pentacyclic chromanes Immunosuppressant Tu, Liang verfasserin aut Cheng, Guiguang verfasserin aut Sa, Houling verfasserin aut Li, Zhenghui verfasserin aut Feng, Tao verfasserin (orcid)0000-0002-1977-9857 aut Zheng, Yongsheng verfasserin (orcid)0000-0002-1019-5521 aut Liu, Jikai verfasserin aut Enthalten in Tetrahedron letters Amsterdam [u.a.] : Elsevier Science, 1959 61 Online-Ressource (DE-627)320459489 (DE-600)2007074-3 (DE-576)094107939 1873-3581 nnns volume:61 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 61 |
| spelling |
10.1016/j.tetlet.2019.151579 doi (DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Li, Na verfasserin aut Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). β-Naphthols [3+3] Cycloaddition Pentacyclic chromanes Immunosuppressant Tu, Liang verfasserin aut Cheng, Guiguang verfasserin aut Sa, Houling verfasserin aut Li, Zhenghui verfasserin aut Feng, Tao verfasserin (orcid)0000-0002-1977-9857 aut Zheng, Yongsheng verfasserin (orcid)0000-0002-1019-5521 aut Liu, Jikai verfasserin aut Enthalten in Tetrahedron letters Amsterdam [u.a.] : Elsevier Science, 1959 61 Online-Ressource (DE-627)320459489 (DE-600)2007074-3 (DE-576)094107939 1873-3581 nnns volume:61 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 61 |
| allfields_unstemmed |
10.1016/j.tetlet.2019.151579 doi (DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Li, Na verfasserin aut Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). β-Naphthols [3+3] Cycloaddition Pentacyclic chromanes Immunosuppressant Tu, Liang verfasserin aut Cheng, Guiguang verfasserin aut Sa, Houling verfasserin aut Li, Zhenghui verfasserin aut Feng, Tao verfasserin (orcid)0000-0002-1977-9857 aut Zheng, Yongsheng verfasserin (orcid)0000-0002-1019-5521 aut Liu, Jikai verfasserin aut Enthalten in Tetrahedron letters Amsterdam [u.a.] : Elsevier Science, 1959 61 Online-Ressource (DE-627)320459489 (DE-600)2007074-3 (DE-576)094107939 1873-3581 nnns volume:61 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 61 |
| allfieldsGer |
10.1016/j.tetlet.2019.151579 doi (DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Li, Na verfasserin aut Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). β-Naphthols [3+3] Cycloaddition Pentacyclic chromanes Immunosuppressant Tu, Liang verfasserin aut Cheng, Guiguang verfasserin aut Sa, Houling verfasserin aut Li, Zhenghui verfasserin aut Feng, Tao verfasserin (orcid)0000-0002-1977-9857 aut Zheng, Yongsheng verfasserin (orcid)0000-0002-1019-5521 aut Liu, Jikai verfasserin aut Enthalten in Tetrahedron letters Amsterdam [u.a.] : Elsevier Science, 1959 61 Online-Ressource (DE-627)320459489 (DE-600)2007074-3 (DE-576)094107939 1873-3581 nnns volume:61 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 61 |
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10.1016/j.tetlet.2019.151579 doi (DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Li, Na verfasserin aut Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes 2020 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). β-Naphthols [3+3] Cycloaddition Pentacyclic chromanes Immunosuppressant Tu, Liang verfasserin aut Cheng, Guiguang verfasserin aut Sa, Houling verfasserin aut Li, Zhenghui verfasserin aut Feng, Tao verfasserin (orcid)0000-0002-1977-9857 aut Zheng, Yongsheng verfasserin (orcid)0000-0002-1019-5521 aut Liu, Jikai verfasserin aut Enthalten in Tetrahedron letters Amsterdam [u.a.] : Elsevier Science, 1959 61 Online-Ressource (DE-627)320459489 (DE-600)2007074-3 (DE-576)094107939 1873-3581 nnns volume:61 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 61 |
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Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes |
| ctrlnum |
(DE-627)ELV003665372 (ELSEVIER)S0040-4039(19)31378-4 |
| title_full |
Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes |
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Li, Na |
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Tetrahedron letters |
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Tetrahedron letters |
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eng |
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500 - Science |
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marc |
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2020 |
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Li, Na Tu, Liang Cheng, Guiguang Sa, Houling Li, Zhenghui Feng, Tao Zheng, Yongsheng Liu, Jikai |
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61 |
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Elektronische Aufsätze |
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Li, Na |
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10.1016/j.tetlet.2019.151579 |
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540 |
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verfasserin |
| title_sort |
diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: efficient assemble of immunosuppressive pentacyclic chromanes |
| title_auth |
Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes |
| abstract |
A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). |
| abstractGer |
A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). |
| abstract_unstemmed |
A base promoted diastereoselective formal [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols towards the synthesis of functionalized pentacyclic indeno[1,2-b]chromen-(4bH)-ones has been developed. This methodology is appreciated in terms of diastereoselectivity and mild conditions. In addition, the immunosuppressive assay indicates that one of the products has selective inhibition on T-cell proliferation (IC50 value of 8.73 μM). |
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| title_short |
Diastereoselective [3 + 3] cycloaddition reaction of 2-arylideneindan-1,3-diones with β-naphthols: Efficient assemble of immunosuppressive pentacyclic chromanes |
| remote_bool |
true |
| author2 |
Tu, Liang Cheng, Guiguang Sa, Houling Li, Zhenghui Feng, Tao Zheng, Yongsheng Liu, Jikai |
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10.1016/j.tetlet.2019.151579 |
| up_date |
2024-07-06T20:23:28.413Z |
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