Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives

被引:2
作者
Gutierrez-Loriente, Agustin [1 ,2 ]
Martin-Alvarez, Jose M. [1 ,3 ]
Prieto, Elena [1 ,2 ]
Andres, Celia [1 ,2 ]
Nieto, Javier [1 ,2 ]
机构
[1] Univ Valladolid, Fac Ciencias, Inst CINQUIMA, Paseo Belen 7, E-47011 Valladolid, Spain
[2] Univ Valladolid, Fac Ciencias, Dept Quim Organ, Paseo Belen 7, E-47011 Valladolid, Spain
[3] Univ Valladolid, Fac Ciencias, Dept Quim Inorgan, Paseo Belen 7, E-47011 Valladolid, Spain
关键词
Asymmetric synthesis; metathesis; oxygen heterocycles; nitrogen heterocycles; chiral auxiliaries; ENANTIOSELECTIVE OLEFIN METATHESIS; REARRANGEMENT METATHESIS; COMPLEXES; EFFICIENT; CONSTRUCTION; ALCOHOLS; BEARING; ETHERS;
D O I
10.1002/adsc.201801454
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Diastereoselective ring-closing metathesis reactions on chiral trienic perhydro-1,3-benzoxazines derived from (-)-8-aminomenthol featuring two diastereotopic olefin chains is described. The diastereochemical outcome of the cyclization appeared to be dependent on the length and position of the olefin chains in perhydro-1,3-benzoxazine, the degree of substitution of the double bonds and the ruthenium catalyst used. After separation of the diastereomers, and removal of the chiral auxiliary, enantiopure oxygen- and nitrogen-containing heterocycles were obtained.
引用
收藏
页码:1042 / 1063
页数:22
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