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Highly Regioselective Aromatic C–H Allylation of N ‑(Arylme..:

Meng-Zeng Zhu (7254881) ; Dong Xie (16842) ; Shi-Kai Tian (1398094)
https://figshare.com/articles/journal_contribution/Highly_Regioselective_Aromatic_C_H_Allylation_of_i_N_i_Arylmethyl_sulfonimides_with_Allyl_Grignard_Reagents_Involving_Benzylic_C_N_Cleavage/15414141. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c02437.s001

RT Journal
T1 <Title>Highly Regioselective Aromatic C–H Allylation of N ‑(Arylmethyl)sulfonimides with Allyl Grignard Reagents Involving Benzylic C–N Cleavage</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_15414141&Exemplar=1&LAN=DE
				
A1 Meng-Zeng Zhu (7254881)
A1 Dong Xie (16842)
A1 Shi-Kai Tian (1398094)
YR 2021
K1 Biochemistry
K1 Medicine
K1 Biotechnology
K1 Virology
K1 Computational Biology
K1 Environmental Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 benzyl electrophiles
K1 2- allylheteroarenes
K1 benzyl electrophile
K1 arylmethyl phosphate
K1 allyl Grignard reagents
K1 palladium-catalyzed
K1 reaction partners
K1 arylmethyl chloride
K1 room temperature
K1 1- allylnaphthalenes
JF https://figshare.com/articles/journal_contribution/Highly_Regioselective_Aromatic_C_H_Allylation_of_i_N_i_Arylmethyl_sulfonimides_with_Allyl_Grignard_Reagents_Involving_Benzylic_C_N_Cleavage/15414141
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c02437.s001
DO https://doi.org/10.1021/acs.orglett.1c02437.s001
SF ELIB - SuUB Bremen

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