Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates
Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Cheng, Su-Fang [verfasserIn] Chen, Bin [verfasserIn] Yang, Xiu-Jie [verfasserIn] Luo, Lin [verfasserIn] Zhang, Li-Ping [verfasserIn] Wu, Li-Zhu [verfasserIn] Tung, Chen-Ho [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2014 |
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| Anmerkung: |
© The Royal Society of Chemistry and Owner Societies 2014 |
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| Übergeordnetes Werk: |
Enthalten in: Photochemical & photobiological sciences - Heidelberg : Springer, 2002, 13(2014), 2 vom: 01. Feb., Seite 261-265 |
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| Übergeordnetes Werk: |
volume:13 ; year:2014 ; number:2 ; day:01 ; month:02 ; pages:261-265 |
| Links: |
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| DOI / URN: |
10.1039/c3pp50326g |
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| Katalog-ID: |
SPR045170770 |
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| 520 | |a Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. | ||
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| 700 | 1 | |a Wu, Li-Zhu |e verfasserin |4 aut | |
| 700 | 1 | |a Tung, Chen-Ho |e verfasserin |4 aut | |
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10.1039/c3pp50326g doi (DE-627)SPR045170770 (SPR)c3pp50326g-e DE-627 ger DE-627 rakwb eng 620 ASE 35.16 bkl 42.14 bkl Cheng, Su-Fang verfasserin aut Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Royal Society of Chemistry and Owner Societies 2014 Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. Chen, Bin verfasserin aut Yang, Xiu-Jie verfasserin aut Luo, Lin verfasserin aut Zhang, Li-Ping verfasserin aut Wu, Li-Zhu verfasserin aut Tung, Chen-Ho verfasserin aut Enthalten in Photochemical & photobiological sciences Heidelberg : Springer, 2002 13(2014), 2 vom: 01. Feb., Seite 261-265 (DE-627)342893742 (DE-600)2072584-X 1474-9092 nnns volume:13 year:2014 number:2 day:01 month:02 pages:261-265 https://dx.doi.org/10.1039/c3pp50326g lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_121 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2093 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2472 GBV_ILN_2522 GBV_ILN_2812 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4700 GBV_ILN_4753 35.16 ASE 42.14 ASE AR 13 2014 2 01 02 261-265 |
| spelling |
10.1039/c3pp50326g doi (DE-627)SPR045170770 (SPR)c3pp50326g-e DE-627 ger DE-627 rakwb eng 620 ASE 35.16 bkl 42.14 bkl Cheng, Su-Fang verfasserin aut Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Royal Society of Chemistry and Owner Societies 2014 Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. Chen, Bin verfasserin aut Yang, Xiu-Jie verfasserin aut Luo, Lin verfasserin aut Zhang, Li-Ping verfasserin aut Wu, Li-Zhu verfasserin aut Tung, Chen-Ho verfasserin aut Enthalten in Photochemical & photobiological sciences Heidelberg : Springer, 2002 13(2014), 2 vom: 01. Feb., Seite 261-265 (DE-627)342893742 (DE-600)2072584-X 1474-9092 nnns volume:13 year:2014 number:2 day:01 month:02 pages:261-265 https://dx.doi.org/10.1039/c3pp50326g lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_121 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2093 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2472 GBV_ILN_2522 GBV_ILN_2812 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4700 GBV_ILN_4753 35.16 ASE 42.14 ASE AR 13 2014 2 01 02 261-265 |
| allfields_unstemmed |
10.1039/c3pp50326g doi (DE-627)SPR045170770 (SPR)c3pp50326g-e DE-627 ger DE-627 rakwb eng 620 ASE 35.16 bkl 42.14 bkl Cheng, Su-Fang verfasserin aut Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Royal Society of Chemistry and Owner Societies 2014 Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. Chen, Bin verfasserin aut Yang, Xiu-Jie verfasserin aut Luo, Lin verfasserin aut Zhang, Li-Ping verfasserin aut Wu, Li-Zhu verfasserin aut Tung, Chen-Ho verfasserin aut Enthalten in Photochemical & photobiological sciences Heidelberg : Springer, 2002 13(2014), 2 vom: 01. Feb., Seite 261-265 (DE-627)342893742 (DE-600)2072584-X 1474-9092 nnns volume:13 year:2014 number:2 day:01 month:02 pages:261-265 https://dx.doi.org/10.1039/c3pp50326g lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_121 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2093 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2472 GBV_ILN_2522 GBV_ILN_2812 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4700 GBV_ILN_4753 35.16 ASE 42.14 ASE AR 13 2014 2 01 02 261-265 |
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10.1039/c3pp50326g doi (DE-627)SPR045170770 (SPR)c3pp50326g-e DE-627 ger DE-627 rakwb eng 620 ASE 35.16 bkl 42.14 bkl Cheng, Su-Fang verfasserin aut Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Royal Society of Chemistry and Owner Societies 2014 Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. Chen, Bin verfasserin aut Yang, Xiu-Jie verfasserin aut Luo, Lin verfasserin aut Zhang, Li-Ping verfasserin aut Wu, Li-Zhu verfasserin aut Tung, Chen-Ho verfasserin aut Enthalten in Photochemical & photobiological sciences Heidelberg : Springer, 2002 13(2014), 2 vom: 01. Feb., Seite 261-265 (DE-627)342893742 (DE-600)2072584-X 1474-9092 nnns volume:13 year:2014 number:2 day:01 month:02 pages:261-265 https://dx.doi.org/10.1039/c3pp50326g lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_121 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2093 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2472 GBV_ILN_2522 GBV_ILN_2812 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4700 GBV_ILN_4753 35.16 ASE 42.14 ASE AR 13 2014 2 01 02 261-265 |
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10.1039/c3pp50326g doi (DE-627)SPR045170770 (SPR)c3pp50326g-e DE-627 ger DE-627 rakwb eng 620 ASE 35.16 bkl 42.14 bkl Cheng, Su-Fang verfasserin aut Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Royal Society of Chemistry and Owner Societies 2014 Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. Chen, Bin verfasserin aut Yang, Xiu-Jie verfasserin aut Luo, Lin verfasserin aut Zhang, Li-Ping verfasserin aut Wu, Li-Zhu verfasserin aut Tung, Chen-Ho verfasserin aut Enthalten in Photochemical & photobiological sciences Heidelberg : Springer, 2002 13(2014), 2 vom: 01. Feb., Seite 261-265 (DE-627)342893742 (DE-600)2072584-X 1474-9092 nnns volume:13 year:2014 number:2 day:01 month:02 pages:261-265 https://dx.doi.org/10.1039/c3pp50326g lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_121 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2093 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2119 GBV_ILN_2129 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2472 GBV_ILN_2522 GBV_ILN_2812 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4367 GBV_ILN_4700 GBV_ILN_4753 35.16 ASE 42.14 ASE AR 13 2014 2 01 02 261-265 |
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Cheng, Su-Fang @@aut@@ Chen, Bin @@aut@@ Yang, Xiu-Jie @@aut@@ Luo, Lin @@aut@@ Zhang, Li-Ping @@aut@@ Wu, Li-Zhu @@aut@@ Tung, Chen-Ho @@aut@@ |
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620 ASE 35.16 bkl 42.14 bkl Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates |
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synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates |
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Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates |
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Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. © The Royal Society of Chemistry and Owner Societies 2014 |
| abstractGer |
Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. © The Royal Society of Chemistry and Owner Societies 2014 |
| abstract_unstemmed |
Abstract Irradiation of (2 R,4 R)-(−)- and (2 S,4 S)-(+)-2,4-pentanediyl-bis-2-naphthoates (1R and 1S, respectively) in organic solutions exclusively results in cubane-like antiHH photodimers in 100% yield. Asymmetric induction with 100% diastereometric excess (de) has been achieved and the absolute configuration of the yielded diastereomers has been established. Moreover, irradiation of (2 R,4 S)-2,4-pentanediyl-bis-2-naphthoate (1M) gives cubane-like synHH photodimers in 100% yield. © The Royal Society of Chemistry and Owner Societies 2014 |
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Synthesis of diastereometrically pure cubane-like photodimers from 2,4-pentanediyl-bis-2-naphthoates |
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