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Regioselective Silylations of Propargyl and Allyl Pivalates..:

Tianyuan Zhang (2501488) ; Suhua Zheng (9509411) ; Taro Kobayashi (11377997).
https://figshare.com/articles/journal_contribution/Regioselective_Silylations_of_Propargyl_and_Allyl_Pivalates_through_Ca-Promoted_Reductive_C_sp_sup_3_sup_O_Bond_Cleavage/16560185. , 2021

Link: https://doi.org/10.1021/acs.orglett.1c02532.s001

RT Journal
T1 <Title>Regioselective Silylations of Propargyl and Allyl Pivalates through Ca-Promoted Reductive C(sp 3 )–O Bond Cleavage</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16560185&Exemplar=1&LAN=DE
				
A1 Tianyuan Zhang (2501488)
A1 Suhua Zheng (9509411)
A1 Taro Kobayashi (11377997)
A1 Hirofumi Maekawa (2723527)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Medicine
K1 Genetics
K1 Biotechnology
K1 Developmental Biology
K1 Hematology
K1 Environmental Sciences not elsewhere classified
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 reductive coupling reaction
K1 promoted reductive c
K1 36 – 77
K1 readily accessible 3
K1 regioselective silylations
K1 regioselective preparation
K1 practical protocol
K1 phenylallyl pivalates
K1 mild catalyst
K1 method represents
K1 handle pivalates
K1 first example
K1 direct application
K1 broad range
K1 bond cleavage
K1 allyl pivalates
JF https://figshare.com/articles/journal_contribution/Regioselective_Silylations_of_Propargyl_and_Allyl_Pivalates_through_Ca-Promoted_Reductive_C_sp_sup_3_sup_O_Bond_Cleavage/16560185
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.1c02532.s001
DO https://doi.org/10.1021/acs.orglett.1c02532.s001
SF ELIB - SuUB Bremen

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