Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks

Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axe...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Wei, Jinding [verfasserIn] Zhu, Minghong [verfasserIn] Zhang, Bo [verfasserIn] Li, Keru [verfasserIn] Zhang, Xiaoke [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis

Übergeordnetes Werk:	Enthalten in: Tetrahedron - Amsterdam [u.a.] : Elsevier Science, 1957, 149
Übergeordnetes Werk:	volume:149

DOI / URN:	10.1016/j.tet.2023.133716

Katalog-ID:	ELV065838009

Internformat


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245	1	0	\|a Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
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520			\|a Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application.
650		4	\|a Atroposelective synthesis
650		4	\|a Atropisomeric indole framework
650		4	\|a Asymmetric synthesis
700	1		\|a Zhu, Minghong \|e verfasserin \|4 aut
700	1		\|a Zhang, Bo \|e verfasserin \|4 aut
700	1		\|a Li, Keru \|e verfasserin \|4 aut
700	1		\|a Zhang, Xiaoke \|e verfasserin \|4 aut
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912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
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
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912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_187
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
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_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
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_4338
912			\|a GBV_ILN_4393
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Indexfelder

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matchkey_str	article:14645416:2023----::eetdacsntooeetvsnhssfxalciahtrbayf
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publishDate	2023
allfields	10.1016/j.tet.2023.133716 doi (DE-627)ELV065838009 (ELSEVIER)S0040-4020(23)00518-5 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Wei, Jinding verfasserin aut Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application. Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis Zhu, Minghong verfasserin aut Zhang, Bo verfasserin aut Li, Keru verfasserin aut Zhang, Xiaoke verfasserin aut Enthalten in Tetrahedron Amsterdam [u.a.] : Elsevier Science, 1957 149 Online-Ressource (DE-627)320459462 (DE-600)2007072-X (DE-576)098253298 1464-5416 nnns volume:149 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 149
spelling	10.1016/j.tet.2023.133716 doi (DE-627)ELV065838009 (ELSEVIER)S0040-4020(23)00518-5 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Wei, Jinding verfasserin aut Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application. Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis Zhu, Minghong verfasserin aut Zhang, Bo verfasserin aut Li, Keru verfasserin aut Zhang, Xiaoke verfasserin aut Enthalten in Tetrahedron Amsterdam [u.a.] : Elsevier Science, 1957 149 Online-Ressource (DE-627)320459462 (DE-600)2007072-X (DE-576)098253298 1464-5416 nnns volume:149 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 149
allfields_unstemmed	10.1016/j.tet.2023.133716 doi (DE-627)ELV065838009 (ELSEVIER)S0040-4020(23)00518-5 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Wei, Jinding verfasserin aut Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application. Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis Zhu, Minghong verfasserin aut Zhang, Bo verfasserin aut Li, Keru verfasserin aut Zhang, Xiaoke verfasserin aut Enthalten in Tetrahedron Amsterdam [u.a.] : Elsevier Science, 1957 149 Online-Ressource (DE-627)320459462 (DE-600)2007072-X (DE-576)098253298 1464-5416 nnns volume:149 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 149
allfieldsGer	10.1016/j.tet.2023.133716 doi (DE-627)ELV065838009 (ELSEVIER)S0040-4020(23)00518-5 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Wei, Jinding verfasserin aut Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application. Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis Zhu, Minghong verfasserin aut Zhang, Bo verfasserin aut Li, Keru verfasserin aut Zhang, Xiaoke verfasserin aut Enthalten in Tetrahedron Amsterdam [u.a.] : Elsevier Science, 1957 149 Online-Ressource (DE-627)320459462 (DE-600)2007072-X (DE-576)098253298 1464-5416 nnns volume:149 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 149
allfieldsSound	10.1016/j.tet.2023.133716 doi (DE-627)ELV065838009 (ELSEVIER)S0040-4020(23)00518-5 DE-627 ger DE-627 rda eng 540 VZ 35.00 bkl Wei, Jinding verfasserin aut Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application. Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis Zhu, Minghong verfasserin aut Zhang, Bo verfasserin aut Li, Keru verfasserin aut Zhang, Xiaoke verfasserin aut Enthalten in Tetrahedron Amsterdam [u.a.] : Elsevier Science, 1957 149 Online-Ressource (DE-627)320459462 (DE-600)2007072-X (DE-576)098253298 1464-5416 nnns volume:149 GBV_USEFLAG_U GBV_ELV SYSFLAG_U 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_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_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 Chemie: Allgemeines VZ AR 149
language	English
source	Enthalten in Tetrahedron 149 volume:149
sourceStr	Enthalten in Tetrahedron 149 volume:149
format_phy_str_mv	Article
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topic_facet	Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis
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author	Wei, Jinding
spellingShingle	Wei, Jinding ddc 540 bkl 35.00 misc Atroposelective synthesis misc Atropisomeric indole framework misc Asymmetric synthesis Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
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topic_title	540 VZ 35.00 bkl Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks Atroposelective synthesis Atropisomeric indole framework Asymmetric synthesis
topic	ddc 540 bkl 35.00 misc Atroposelective synthesis misc Atropisomeric indole framework misc Asymmetric synthesis
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title	Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
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title_full	Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
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title_sort	recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
title_auth	Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
abstract	Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application.
abstractGer	Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application.
abstract_unstemmed	Axially chiral heterobiaryl featuring indole framework are promising structure in pharmaceutically active molecule, many natural product, and asymmetric catalysis field. Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application.
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title_short	Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks
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author2	Zhu, Minghong Zhang, Bo Li, Keru Zhang, Xiaoke
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doi_str	10.1016/j.tet.2023.133716
up_date	2024-07-07T00:25:32.305Z
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Thus, a variety of protocols have been realized for the construction these challenging scaffolds with C–C, C–N, and N–N chiral axes. So far, a series of reviews on the synthesis of axially chiral compounds have been reported. However, atroposelective construction of indole subunit was rarely disclosed. Herein, we summarized the recent advance in atroposelective synthesis of axially chiral heterobiaryl featuring indole skeleton dividing these strategies into four categories. This review mainly discussed the related mechanism, scope, and application.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Atroposelective synthesis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Atropisomeric indole framework</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Asymmetric synthesis</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhu, Minghong</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, Bo</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Li, Keru</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhang, 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Recent advances in atroposelective synthesis of axially chiral heterobiaryl featuring indole frameworks

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