Stereoselective Total Synthesis of 1,4-Dideoxy-1,4-imino-L-ribitol by an Intramolecular Ring Opening of Epoxide with a Tethered Amide

Stereoselective total synthesis of 1,4-dideoxy-1,4-imino-L-ribitol has been accomplished from D -glucose. The key step involved in this synthesis is the regioselective ring-opening of the epoxide with a tethered amido group to give the N -tosyl-3,6-dideoxy-3,6-imino-1,2- O -isopropylidene-α-D-glucof...

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Үндсэн зохиолчид:	Chaya N Dhudmal, Dhanraj O Biradar, Maddipatla V. Satyanarayana, Basi V Subba Reddy
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	SAGE Publishing 2018-08-01
Цуврал:	Natural Product Communications
Онлайн хандалт:	https://doi.org/10.1177/1934578X1801300821
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!