![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1395.gif)
4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane (in CH2Cl2) | dichloromethane | N Parameter: -0.64 sN Parameter: 1.10 | ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1396.gif)
potassium allyltrifluoroborate (in MeCN) | MeCN | N Parameter: 5.29 sN Parameter: 0.87 | ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1397.gif)
lithium 2-allyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN) | MeCN | N Parameter: 8.71 sN Parameter: 0.80 | ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1398.gif)
lithium 2-allyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN) | MeCN | N Parameter: 11.20 sN Parameter: 0.64 | ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1399.gif)
lithium (E)-2-(3,5-bis(trifluoromethyl)phenyl)-2-(but-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN) | MeCN | N Parameter: 9.49 sN Parameter: 0.82 | ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240 |