In 2020.0 SYNTHESIS-STUTTGART published article about POLYSUBSTITUTED FURANS; CYCLOADDITION; CYCLIZATION; CONDENSATION; GENERATION; EFFICIENT; ACCESS in [Dobesch, Matthias; Greiner, Julian; Maas, Gerhard] Ulm Univ, Inst Organ Chem 1, Albert Einstein Allee 11, D-89081 Ulm, Germany in 2020.0, Cited 54.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. Recommanded Product: Benzyl Alcohol
Compounds incorporating a 4-aza-8-oxabicyclo[3.2.1]oct-6-en-2-one moiety, which were prepared by a tandem carbenoid carbonyl ylide cyclization/[3+2]-cycloaddition reaction from ethyl 2-diazo-3-oxo-4-phthalimidobutanoates, undergo a nucleophile-induced two-bond ring cleavage when treated with protic heteronucleophiles. In this manner, tetrasubstituted furantricarboxylates, tethered with alpha-amino acids, esters, thioesters, and amides by a 2-carbonylphenyl moiety, are obtained.
Welcome to talk about 100-51-6, If you have any questions, you can contact Dobesch, M; Greiner, J; Maas, G or send Email.. Recommanded Product: Benzyl Alcohol
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles