1245507-48-5Relevant articles and documents
Preparation of (+)-biotin: Process development and scale-up
Xiong, Fei,Li, Jin,Li, Gen,Song, Bo,Zhou, Yu-Xiao,Chen, Fen-Er,Li, Dan
, p. 544 - 551 (2016)
A practical asymmetric total synthesis of (+)-biotin based upon the chiral bifunctional sulfamide 8-promoted enantioselective anhydride desymmetrization has been achieved via the key chiral intermediacy of (3aS, 6aR)-1,3-bis(4-methoxybenzyl)tetrahydro-4H-thieno[3,4-d]imidazole-2,4(1H)-dione (4). In addition, the installation of the 4-carboxybutyl side chain at C-4 position of 4 was efficiently introduced by an improved C4+C1 strategy.
BIOMOLECULAR LABELLING USING MULTIFUNCTIONAL BIOTIN ANALOGUES
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Page/Page column 39-40, (2010/10/03)
Novel biotin analogues, such as 2-Azidobiotin, comprising the ureido ring of natural biotin with the thiophene ring, optionally modified, and a modified sidechain having a functional end group, preferably selected from the group consisting of a carboxylic