Shukla, Nalin’s team published research in Trends in Carbohydrate Research in 2011 | CAS: 99409-32-2

Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranoside(cas: 99409-32-2) belongs to indole.The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades.Safety of Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranosideThey are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.

In 2011,Trends in Carbohydrate Research included an article by Shukla, Nalin; Srivastava, Sanjay; Khare, Naveen K.; Mukhopadhay, Balaram; Khare, Anakshi. Safety of Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranoside. The article was titled 《Concise synthesis of a di- and a trisaccharide related to the pentasaccharide repeating unit of the O-antigen from E. coli O141》. The information in the text is summarized as follows:

Synthesis of a di- and a trisaccharide related to the pentasaccharide repeating unit of the O-antigen from E. coli O141 have been accomplished using com. available D-mannose, L-rhamnose and D-glucose. These di and trisaccharides have been synthesized as their p-methoxyphenyl and allyl glycosides, resp., which can be cleaved selectively for further conjugation with suitable aglycon. In the part of experimental materials, we found many familiar compounds, such as Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranoside(cas: 99409-32-2Safety of Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranoside)

Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranoside(cas: 99409-32-2) belongs to indole.The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades.Safety of Ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-thioglucopyranosideThey are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.

Referemce:
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