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Enantioselective Domino Reaction of 3‑Vinylindole and p ‑Qu..:

Ji-Gang Gao (4617466) ; Xu-Kai Guan (6909452) ; Dong-Yang Sun (7431620)...
https://figshare.com/articles/journal_contribution/Enantioselective_Domino_Reaction_of_3_Vinylindole_and_i_p_i_Quinone_Methides_Enabled_by_Chiral_Imidodiphosphoric_Acids_Asymmetric_Synthesis_of_Multisubstituted_3_Indolyl_Cyclopenta_i_b_i_indoles/14717650. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c01600.s001

RT Journal
T1 <Title>Enantioselective Domino Reaction of 3‑Vinylindole and p ‑Quinone Methides Enabled by Chiral Imidodiphosphoric Acids: Asymmetric Synthesis of Multisubstituted 3‑Indolyl Cyclopenta[ b ]indoles</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14717650&Exemplar=1&LAN=DE
				
A1 Ji-Gang Gao (4617466)
A1 Xu-Kai Guan (6909452)
A1 Dong-Yang Sun (7431620)
A1 Heng Zhang (320479)
A1 Wen-Hua Mi (10911379)
A1 Xiang-Shuo Qin (7431623)
A1 Guang-Liang Zhang (7431626)
A1 Suoqin Zhang (1710148)
YR 2021
K1 Biochemistry
K1 Medicine
K1 Microbiology
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Sociology
K1 Immunology
K1 Developmental Biology
K1 Plant Biology
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Information Systems not elsewhere classified
K1 enantioselectivitie
K1 cyclopenta
K1 stereoselective method
K1 cascade
K1 assembly
K1 indolyl
K1 Vinylindole
K1 Multisubstituted
K1 3- vinylindole
K1 diastereoselectivitie
K1 Chiral Imidodiphosphoric Acids
K1 Quinone
K1 Asymmetric Synthesis
K1 series
K1 molecule
K1 Enantioselective Domino Reaction
K1 Enabled
K1 yield
K1 chiral centers
K1 dr
K1 preparation
K1 quinone methide
K1 Methide
JF https://figshare.com/articles/journal_contribution/Enantioselective_Domino_Reaction_of_3_Vinylindole_and_i_p_i_Quinone_Methides_Enabled_by_Chiral_Imidodiphosphoric_Acids_Asymmetric_Synthesis_of_Multisubstituted_3_Indolyl_Cyclopenta_i_b_i_indoles/14717650
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c01600.s001
DO https://doi.org/10.1021/acs.orglett.1c01600.s001
SF ELIB - SuUB Bremen

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