Expeditious synthesis of seven-membered iminocyclitols
摘要:
A concise synthesis of an azepanetriol and an octahydropyrrolo[1,2-a]azepinepentol. by nitrone addition to a pent-4-enofuranoside derived from D-ribose, Followed by reductive opening of the isoxazolidine ring formed. is reported. (C). 2001 Elsevier Science Ltd. All rights reserved.
Expeditious synthesis of seven-membered iminocyclitols
摘要:
A concise synthesis of an azepanetriol and an octahydropyrrolo[1,2-a]azepinepentol. by nitrone addition to a pent-4-enofuranoside derived from D-ribose, Followed by reductive opening of the isoxazolidine ring formed. is reported. (C). 2001 Elsevier Science Ltd. All rights reserved.
Expeditious synthesis of seven-membered iminocyclitols
作者:John K Gallos、Soultana C Demeroudi、Constantina C Stathopoulou、Constantinos C Dellios
DOI:10.1016/s0040-4039(01)01587-8
日期:2001.10
A concise synthesis of an azepanetriol and an octahydropyrrolo[1,2-a]azepinepentol. by nitrone addition to a pent-4-enofuranoside derived from D-ribose, Followed by reductive opening of the isoxazolidine ring formed. is reported. (C). 2001 Elsevier Science Ltd. All rights reserved.