Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tien Ha, Trieu"'
Publikováno v:
ACS Omega, Vol 3, Iss 7, Pp 8243-8252 (2018)
Externí odkaz:
https://doaj.org/article/0e9a60b249c74e568d08eafca502ce9a
Publikováno v:
ACS Omega, Vol 3, Iss 1, Pp 544-553 (2018)
Externí odkaz:
https://doaj.org/article/486c5615aa8d48d2a549d8ea830acbb6
Publikováno v:
ACS Omega
ACS Omega, Vol 3, Iss 7, Pp 8243-8252 (2018)
ACS Omega, Vol 3, Iss 7, Pp 8243-8252 (2018)
A green chemical method for mild oxidation of 1,2,3,4-tetrahydroisoquinolines (THIQs) and 3,4-dihydroisoquinolines (DHIQs) has been developed using air (O2) as a clean oxidant. DHIQs and THIQs could be efficiently oxidized to isoquinolines in dimethy
Publikováno v:
RSC Advances. 8:6834-6839
A mild, efficient and environmentally benign method for synthesis of aromatic β-carbolines via Cu(II)-catalyzed oxidation of 1,2,3,4-tetrahydro-β-carbolines (THβCs) was developed, in which air (O2) was used as the clean oxidant. This method has ad
Publikováno v:
ACS Omega, Vol 3, Iss 1, Pp 544-553 (2018)
A green chemical method for the conversion of 3,4-dihydro-β-carbolines to β-carbolines has been developed using air as the oxidant. With 15 mol % CuBr2 as the catalyst, 3,4-dihydro-β-carbolines could be efficiently oxidized to β-carbolines in dim
Autor:
Tian-Zhuo, Meng, Jie, Zheng, Tien Ha, Trieu, Bo, Zheng, Jia-Jia, Wu, Yi, Zhang, Xiao-Xin, Shi
Publikováno v:
ACS Omega
A green chemical method for the conversion of 3,4-dihydro-β-carbolines to β-carbolines has been developed using air as the oxidant. With 15 mol % CuBr2 as the catalyst, 3,4-dihydro-β-carbolines could be efficiently oxidized to β-carbolines in dim
Publikováno v:
Synthetic Communications. 43:3141-3152
An efficient, mild, benign, and practical method for one-pot conversion of N-tosyl-1,4,5,6-tetrahydropyrimidines into pyrimidines is discussed in detail. In this method, N-tosyl-1,4,5,6-tetrahydropyrimidines are first prepared via N-tosylation of tet
Publikováno v:
Tetrahedron: Asymmetry. 22:1865-1873
An efficient and general strategy for the highly stereoselective synthesis of HR22C16-like mitotic kinesin Eg5 inhibitors 1 from both l - and d -tryptophan methyl ester hydrohalides is described. (1R,3S)-trans-1,3-Disubstituted 1,2,3,4-tetrahydro-β-
Publikováno v:
ChemInform. 44
The first total synthesis of eudistomin Y7 (Ia) and total syntheses of eudistomins Y1-Y6 (Ib-g) are described.