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Highly Enantioselective Synthesis of Pyrroloindolones and P..:

Xiao-Yong Duan (1457578) ; Zhaohui Tian (5068625) ; Binghao Liu (10692175)...
https://figshare.com/articles/journal_contribution/Highly_Enantioselective_Synthesis_of_Pyrroloindolones_and_Pyrroloquinolinones_via_an_i_N_i_Heterocyclic_Carbene-Catalyzed_Cascade_Reaction/14474323. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c01203.s001

RT Journal
T1 <Title>Highly Enantioselective Synthesis of Pyrroloindolones and Pyrroloquinolinones via an N ‑Heterocyclic Carbene-Catalyzed Cascade Reaction</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14474323&Exemplar=1&LAN=DE
				
A1 Xiao-Yong Duan (1457578)
A1 Zhaohui Tian (5068625)
A1 Binghao Liu (10692175)
A1 Tao He (23919)
A1 Liang-Liang Zhao (4244971)
A1 Mengdie Dong (10692178)
A1 Pengna Zhang (10692181)
A1 Jing Qi (235750)
YR 2021
K1 Biochemistry
K1 Microbiology
K1 Molecular Biology
K1 Neuroscience
K1 Infectious Diseases
K1 Virology
K1 Chemical Sciences not elsewhere classified
K1 indole -7-carboxaldehyde aldimines
K1 Pyrroloindolone
K1 enal
K1 Carbene-Catalyzed
K1 substrate scope
K1 Pyrroloquinolinone
K1 NHC-catalyzed
K1 assembly
K1 Heterocyclic
K1 Cascade
K1 indole -2-carboxaldehyde aldimines
K1 yield
K1 Enantioselective Synthesis
K1 enantioselectivitie
K1 pyrroloquinolinones derivatives
JF https://figshare.com/articles/journal_contribution/Highly_Enantioselective_Synthesis_of_Pyrroloindolones_and_Pyrroloquinolinones_via_an_i_N_i_Heterocyclic_Carbene-Catalyzed_Cascade_Reaction/14474323
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c01203.s001
DO https://doi.org/10.1021/acs.orglett.1c01203.s001
SF ELIB - SuUB Bremen

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