21035-81-4Relevant articles and documents
Desymmetric hydrogenation of a meso-cyclic acid anhydride toward biotin synthesis
Yoshimura, Masahiro,Tsuda, Kazuomi,Nakatsuka, Hiroshi,Yamamura, Tomoya,Kitamura, Masato
scheme or table, p. 10006 - 10010 (2012/02/15)
Catalytic reactivity in the hydrogenation of a cyclic anhydride to a biotin synthetic intermediate has been investigated on the basis of Lyons' original method using Wilkinson Ru complex, revealing the high performance of DPPF and XANTPHOS diphosphines possessing wide bite angles. The results have shown a new trail for design of the corresponding asymmetric catalysts, and the potential utility of (S,S)-Et-FerroTANE and (S,S)-(R,R)-Ph-TRAP has been demonstrated.
Highly effective resolution of 1,3-dibenzyl-6-hydroxy-3,3a,6,6a-tetrahydroy-1H-furo[3,4-d]imidazole-2 ,4-dione, an intermediate for biotin, with optically active amines and reutilization of the unwanted epimer
Senuma,Fujii,Seto,Okamura,Date,Kinumaki
, p. 882 - 887 (2007/10/02)
-