1046148-30-4Relevant academic research and scientific papers
Difunctional additions to 1-cyclopropylallenes: an efficient and stereospecific method for the synthesis of 2,6-difunctional-1,3-hexadienes
Meng, Bo,Yu, Lei,Huang, Xian
supporting information; scheme or table, p. 1947 - 1950 (2009/09/06)
The difunctional additions of electrophiles and nucleophiles to 1-cyclopropylallenes were investigated. Two different functional groups were introduced at the same time to give 2,6-difunctional-1,3-hexadienes stereoselectively in good yields.
Electrophilic addition to 1-cyclopropylallenes: A highly efficient and stereoselective method for the preparation of 6-substituted-1,3-hexadienes
Yu, Lei,Meng, Bo,Huang, Xian
scheme or table, p. 1331 - 1334 (2009/04/06)
Electrophilic additions to 1-cyclopropylallenes were investigated, providing an efficient and stereoselective method for the synthesis of 6-substituted-1,3-hexadienes. Georg Thieme Verlag Stuttgart.
Halohydroxylation of 1-cyclopropylallenes: An efficient and stereoselective method for the preparation of multisubstituted olefins
Yu, Lei,Meng, Bo,Huang, Xian
, p. 6895 - 6898 (2008/12/22)
(Chemical Equation Presented) The halohydroxylation of 1-cyclopropylallenes would generate two multisubstituted C=C double bonds and at the same time stereoselectively gives 5-halohexa-3,5-dien-1-ols in moderate to good yields. The latter could be transfo
