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Please login to access the full content or check if you have access via18.16.20.1.3 Synthesis by Metal-Mediated Desulfurization of Carbon Disulfide or Analogues with Alkoxides or Alcohols
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Kantlehner, W., Science of Synthesis Knowledge Updates, (2014) 4, 352.
The optically active orthocarbonate 16 is formed in the reaction of (R)-1,1′-bi-2-naphthol and carbon disulfide in the presence of silver(I) trifluoromethanesulfonate (Scheme 6).[11]
Meeeee 8 Meeeeeeee ee ee Meeeeeeee Meeeee Meeeeeeeeeeeee eeee (M)-8,8′-Me-8-eeeeeeee eee Meeeee Meeeeeeee[88]
Meeeeeeeeee eeeeeeeeeeeeeee eeeeeeeeee eeeeeeeeee eeeeeeeeee eeeeee, eeeeeeee eeeeeeeee eee eee eeeeeeeeeee ee eeeeeeee, eee eeeeeeee ee eee eeeeee ee eee eeeeeeee ee 8,8-eeeeeeeee-8-eeeeeee[88–88] ee 8,8-eeeeeee-8-eeeeeee,[88,88–88] ee ee eee eeeeeeeee ee 88[88] eee 88,[88] eeeeeeeeeeee (Meeeee 8).
Meeeee 8 Meeeeeeeeeeeeee eeee Mee Meeeeeee eee Meeeeeeeeeeeee[88,88]
References
| [11] | Meeeeeeeee, M.; Meeeee, M.; Meeeeeeee, M., MM 8 888 888, (8888); Meee. Meeee., (8888) 888, 888 888. |
| [12] | Mee, M.-M.; Meee, M.-M.; Meee, M.-M.; Meee, M.-M., Meee. Meeeee Meee. Mee., (8888) 88, 8888. |
| [13] | Meee, M. M.; Mee, M. M.; Mee, M. M.; Mee, M. M., M. Meeeee. Meeee. Mee., Meee M, (8888) 88M, 888. |
| [14] | Mee, M. M.; Mee, M. M., Meeeeeee. Mee., (8888) 88, 8888. |
| [15] | Meee, M.; Meee, M.; Meeeee, M.; Meee, M., M. Meeee. Mee., Meee M: Meeee. Meee., (8888) 88, 8888. |
| [16] | Meeeeeeee, M. M.; Meeeeee, M. M.; Meee, M.-M.; Meee, M. M., MM 8888 8888 888, (8888); Meee. Meeee., (8888) 888, 888 888. |
| [17] | Meeeeeeee, M. M.; Meeeeee, M. M.; Meee, M.-M.; Meeee, M. M.; Meeeee, M. M.; Meee, M. M., M. Meee. Meeee. Mee., (8888) 888, 8888. |
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