Special Volume in Memory of Hidetoshi Yamada Part 2
-10%
portes grátis
Special Volume in Memory of Hidetoshi Yamada Part 2
Baker, David C.
Elsevier Science & Technology
12/2022
182
Dura
Inglês
9780323985970
15 a 20 dias
450
Descrição não disponível.
1. Automated and/or Electrochemical Synthesis Toshiki Nokami 2. In Vivo Chemistry Katsunori Tanaka 3. Pseudo-Glycoconjugates with C-Glycoside linkage Go Hirai 4. Boron-Mediated Aglycon Delivery (BMAD) for the Stereoselective Synthesis of 1,2-cis Glycosides Daisuke Takahashi 5. Conformationally Restricted Donors for Stereselective Glycosylation Kaname SASAKI
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
1,2-cis Glycosides; Anomeric radicals; Artificial metalloenzymes; BMAD; Boron-mediated aglycon delivery; Cancer therapy; Cell targeting; C-glycoside analogs; Conformation; Conformational analysis; Continuum of mechanisms; Coupling reaction; Cyclic oligosaccharides; Cyclodextrin; Electrochemical polyglycosylation-isomerization-cyclization; Fluorine-containing C-glycosides; Glycan-modified human serum albumin; Glycolipids; Glycosyl cations; Glycosyl donors; Glycosylation; Kinetic pathway; Natural glycosides; Nucleophilic substitution; Organic synthesis; Protective groups; Regioselective; Remote participation; SN2-SN1 borderline; Stereoelectronic effects; Stereoselective; Stereoselectivity; Steric effects; Synthesis; Therapeutic in vivo synthetic chemistry; Total synthesis
1. Automated and/or Electrochemical Synthesis Toshiki Nokami 2. In Vivo Chemistry Katsunori Tanaka 3. Pseudo-Glycoconjugates with C-Glycoside linkage Go Hirai 4. Boron-Mediated Aglycon Delivery (BMAD) for the Stereoselective Synthesis of 1,2-cis Glycosides Daisuke Takahashi 5. Conformationally Restricted Donors for Stereselective Glycosylation Kaname SASAKI
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
1,2-cis Glycosides; Anomeric radicals; Artificial metalloenzymes; BMAD; Boron-mediated aglycon delivery; Cancer therapy; Cell targeting; C-glycoside analogs; Conformation; Conformational analysis; Continuum of mechanisms; Coupling reaction; Cyclic oligosaccharides; Cyclodextrin; Electrochemical polyglycosylation-isomerization-cyclization; Fluorine-containing C-glycosides; Glycan-modified human serum albumin; Glycolipids; Glycosyl cations; Glycosyl donors; Glycosylation; Kinetic pathway; Natural glycosides; Nucleophilic substitution; Organic synthesis; Protective groups; Regioselective; Remote participation; SN2-SN1 borderline; Stereoelectronic effects; Stereoselective; Stereoselectivity; Steric effects; Synthesis; Therapeutic in vivo synthetic chemistry; Total synthesis
