Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement
By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields.
Autor*in: |
Takemura, Hiroyuki [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: Continuing Medical Education Program - 2013, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:61 ; year:2020 ; number:13 ; day:26 ; month:03 ; pages:0 |
Links: |
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DOI / URN: |
10.1016/j.tetlet.2020.151673 |
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ELV049635875 |
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10.1016/j.tetlet.2020.151673 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001427.pica (DE-627)ELV049635875 (ELSEVIER)S0040-4039(20)30092-7 DE-627 ger DE-627 rakwb eng 610 VZ 540 VZ 35.00 bkl Takemura, Hiroyuki verfasserin aut Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement 2020 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. Chapman rearrangement Elsevier Cyclophanes Elsevier Macrocycles Elsevier [1 n ]Paracyclophanes Elsevier Morikawa, Akino oth Tanaka, Mari oth Tatsumi, Akane oth Kubota, Yukiko oth Kaji, Natsuko oth Hasegawa, Ayako oth Kumamoto, Fumiko oth Obara, Tomoko oth Iwanaga, Tetsuo oth Sako, Katsuya oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:61 year:2020 number:13 day:26 month:03 pages:0 https://doi.org/10.1016/j.tetlet.2020.151673 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 61 2020 13 26 0326 0 |
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10.1016/j.tetlet.2020.151673 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001427.pica (DE-627)ELV049635875 (ELSEVIER)S0040-4039(20)30092-7 DE-627 ger DE-627 rakwb eng 610 VZ 540 VZ 35.00 bkl Takemura, Hiroyuki verfasserin aut Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement 2020 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. Chapman rearrangement Elsevier Cyclophanes Elsevier Macrocycles Elsevier [1 n ]Paracyclophanes Elsevier Morikawa, Akino oth Tanaka, Mari oth Tatsumi, Akane oth Kubota, Yukiko oth Kaji, Natsuko oth Hasegawa, Ayako oth Kumamoto, Fumiko oth Obara, Tomoko oth Iwanaga, Tetsuo oth Sako, Katsuya oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:61 year:2020 number:13 day:26 month:03 pages:0 https://doi.org/10.1016/j.tetlet.2020.151673 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 61 2020 13 26 0326 0 |
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10.1016/j.tetlet.2020.151673 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001427.pica (DE-627)ELV049635875 (ELSEVIER)S0040-4039(20)30092-7 DE-627 ger DE-627 rakwb eng 610 VZ 540 VZ 35.00 bkl Takemura, Hiroyuki verfasserin aut Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement 2020 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. Chapman rearrangement Elsevier Cyclophanes Elsevier Macrocycles Elsevier [1 n ]Paracyclophanes Elsevier Morikawa, Akino oth Tanaka, Mari oth Tatsumi, Akane oth Kubota, Yukiko oth Kaji, Natsuko oth Hasegawa, Ayako oth Kumamoto, Fumiko oth Obara, Tomoko oth Iwanaga, Tetsuo oth Sako, Katsuya oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:61 year:2020 number:13 day:26 month:03 pages:0 https://doi.org/10.1016/j.tetlet.2020.151673 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 61 2020 13 26 0326 0 |
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10.1016/j.tetlet.2020.151673 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001427.pica (DE-627)ELV049635875 (ELSEVIER)S0040-4039(20)30092-7 DE-627 ger DE-627 rakwb eng 610 VZ 540 VZ 35.00 bkl Takemura, Hiroyuki verfasserin aut Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement 2020 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. Chapman rearrangement Elsevier Cyclophanes Elsevier Macrocycles Elsevier [1 n ]Paracyclophanes Elsevier Morikawa, Akino oth Tanaka, Mari oth Tatsumi, Akane oth Kubota, Yukiko oth Kaji, Natsuko oth Hasegawa, Ayako oth Kumamoto, Fumiko oth Obara, Tomoko oth Iwanaga, Tetsuo oth Sako, Katsuya oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:61 year:2020 number:13 day:26 month:03 pages:0 https://doi.org/10.1016/j.tetlet.2020.151673 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 61 2020 13 26 0326 0 |
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Syntheses of diaza(hetera)2[1.1.1.1]paracyclophanes by Chapman rearrangement |
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By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. |
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By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. |
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By applying the Chapman rearrangement, highly strained diaza[1.1.1.1]PCPs containing heteroatoms were successfully synthesized in moderate yields. |
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