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1 Ergebnisse
1
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
Regioselective Silylations of Propargyl and Allyl Pivalates through Ca-Promoted Reductive C(sp 3 )–O Bond Cleavage
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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