1356144-05-2Relevant academic research and scientific papers
Consecutive reactions between methyl 3-dehydroshikimiate, amines and 1,2-dichloroalkanes under microwave conditions: A practical, one-pot construction of N-substituted dihydrobenzoxazines
Zhang, Ensheng,Xu, Tianlong,Wang, Dejian,Huang, Tongkun,Yuan, Mu,Li, Jun,Zou, Yong
, p. 10022 - 10027 (2014/03/21)
A biomass-involved, one-pot, two-step protocol for the synthesis of N-substituted 3,4-dihydro-2H-1,4-benzoxazines has been developed. A wide range of new compounds have been efficiently synthesized in moderate to excellent yields via the three-component consecutive reactions between methyl 3-dehydroshikimiate (3-MDHS), amines and 1,2-dichloroalkanes in short reaction times under microwave conditions.
Biomass-involved, facile and one-pot synthesis of N-aryl-2(3H)- benzoxazolones from methyl 3-dehydroshikimiate
Zhang, Ensheng,Zhang, Xuejing,Cai, Yuchen,Wang, Dejian,Xu, Tianlong,Li, Jun,Yan, Ming,Zou, Yong
, p. 39020 - 39029 (2014/11/07)
A facile and one-pot method for the synthesis of N-aryl-2(3H)- benzoxazolones via microwave-assisted consecutive reactions between the biomass-derived methyl 3-dehydroshikimiate (3-MDHS), anilines and bis(trichloromethyl) carbonate (BTC) is reported. The protocol includes the efficient generation of the platform compounds N-arylated 2-aminophenols, followed by the smooth annulation reaction induced by BTC. This sequential process represents a metal-free, sustainable and functional group compatible method for the rapid construction of N-aryl-2(3H)-benzoxazolones. the Partner Organisations 2014.
Biomass-involved, facile and one-pot synthesis of N-aryl-2(3H)-benzoxazolones from methyl 3-dehydroshikimiate
Zhang, Ensheng,Zhang, Xuejing,Cai, Yuchen,Wang, Dejian,Xu, Tianlong,Li, Jun,Yan, Ming,Zou, Yong
, p. 39020 - 39029 (2014/12/11)
A facile and one-pot method for the synthesis of N-aryl-2(3H)-benzoxazolones via microwave-assisted consecutive reactions between the biomass-derived methyl 3-dehydroshikimiate (3-MDHS), anilines and bis(trichloromethyl) carbonate (BTC) is reported. The protocol includes the efficient generation of the platform compounds N-arylated 2-aminophenols, followed by the smooth annulation reaction induced by BTC. This sequential process represents a metal-free, sustainable and functional group compatible method for the rapid construction of N-aryl-2(3H)-benzoxazolones. This journal is
Bio-based synthesis of secondary arylamines from (-)-shikimic acid
Wu, Wei,Zou, Yong,Chen, Yu,Li, Jun,Lv, Zeliang,Wei, Wen,Huang, Tongkun,Liu, Xianke
supporting information; experimental part, p. 363 - 370 (2012/04/10)
A specific family of secondary arylamines, including diarylamines and arylalkylamines have been synthesized in good yields starting from the renewable and biomass-based feedstock (-)-shikimic acid (1). The tandem cross-coupling and aromatization reactions
