Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Glycol cleavage"'
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 78:11-27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ea90f5d7d0d8d9fa3eefa6a7c7719f6
https://doi.org/10.5059/yukigoseikyokaishi.78.11
https://doi.org/10.5059/yukigoseikyokaishi.78.11
Autor:
Yoshikazu Kimura, Kouta Adachi, Kento Yamazaki, Katsuya Saito, Masayuki Kirihara, Rie Osugi, Ryoji Matsushima
Publikováno v:
The Journal of organic chemistry. 84(12)
Sodium hypochlorite pentahydrate (NaOCl·5H2O) can be used toward the efficient glycol cleavage of trans-cyclic glycols, which are generally resistant to this transformation. Interestingly, the reaction of cis-cyclic glycols with NaOCl·5H2O is slowe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5030e11517ed44b6ef24bf60b3a56359
https://pubmed.ncbi.nlm.nih.gov/31117583
https://pubmed.ncbi.nlm.nih.gov/31117583
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
European Journal of Organic Chemistry. 2015:7892-7918
We studied the steric course of aldol additions of CpTiCl2 (novel) or Bu2B enolates of the unsubstituted δ-lactone and of the four monomethylated δ-lactones to isobutyraldehyde, crotonaldehyde, and para-bromobenzaldehyde. The titanium enolates reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a72f90d6770c52fd29e4273749673602
https://doi.org/10.1002/ejoc.201501128
https://doi.org/10.1002/ejoc.201501128
Publikováno v:
Synthesis. 46:3283-3308
This review focuses on the application of glycol cleavage reactions in the synthesis and derivatization of complex natural products. Reagent classics as well as recent developments are discussed. 1 Introduction 2 Mechanistic Aspects 3 Reagents and Ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::517404e22cfe30c13e322c1c7ee89a4d
https://doi.org/10.1055/s-0033-1338650
https://doi.org/10.1055/s-0033-1338650
Autor:
Ian Cumpstey
Publikováno v:
ISRN Organic Chemistry
This review covers methods for modifying the structures of polysaccharides. The introduction of hydrophobic, acidic, basic, or other functionality into polysaccharide structures can alter the properties of materials based on these substances. The dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee1ddfad920962ce9779fc0c10a7b165
https://doi.org/10.1155/2013/417672
https://doi.org/10.1155/2013/417672
Publikováno v:
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2017, 5 (4), pp.3214-3222. ⟨10.1021/acssuschemeng.6b02979⟩
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2017, 5 (4), pp.3214-3222. ⟨10.1021/acssuschemeng.6b02979⟩
International audience; A novel catalyst, EcoMnOx, was prepared from waste biomass of Mn-hyperaccumulating plants. The valorization of this Mn-rich biomass is an alternative to its costly usual disposing and provides a new source of Mn. Extracted met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cdbe34066a43df05558bacee9f68fab
https://hal.archives-ouvertes.fr/hal-03779354
https://hal.archives-ouvertes.fr/hal-03779354
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
European Journal of Organic Chemistry. 2013:1346-1355
Herein, we report on the first enantioselective synthesis of the sparteine-type alkaloids virgidivarine (1) and virgiboidine (2). The stereoselective construction of the challenging dipiperidine core within 1 and 2 was realized by applying an intramo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d317bae33a6fa556ca395ea5f5da650f
https://doi.org/10.1002/ejoc.201201516
https://doi.org/10.1002/ejoc.201201516
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 31:763-782
An inexpensive and much improved protocol has been developed for the synthesis of protected morpholino monomers from unprotected ribonucleosides in high overall yield, using oxidative glycol cleavage and reductive amination strategy. Unlike the previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cbae5305e87e7d2d0e3920bf6db1f85
https://doi.org/10.1080/15257770.2012.724491
https://doi.org/10.1080/15257770.2012.724491