869354-98-3Relevant academic research and scientific papers
AN EFFICIENT SYNTHESIS OF (2S,3R)- AND (2S,3S)-SPHINGOSINE
Obayashi, Michio,Schlosser, Manfred
, p. 1715 - 1718 (1985)
A straightforward sequence of reactions allows the conversion of D(+)-Mannose and D(+)-ribono-1,4-lactone into "erythro"-(2S,3R)- and "threo"-(2S,3S)-sphingosine, respectively.
Synthesis of Structurally Diverse Substituted Aziridinyl Glycoconjugates via Base-Mediated One-Pot Post-Ugi Cyclization
Sangwan, Rekha,Dubey, Atul,Prajapati, Gurudayal,Ampapathi, Ravi Sankar,Mandal, Pintu Kumar
supporting information, p. 2859 - 2862 (2019/04/25)
The base-promoted intramolecular cyclization of Ugi-azide adduct has been demonstrated for the synthesis of highly substituted aziridinyl glycoconjugates in one pot. The reactions are scalable and efficient and have an operationally simple broad substrate
