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Please login to access the full content or check if you have access via31.5.2.3.2.1 Variation 1: 1,4-Addition of Trialkylboranes
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Marsini, M. A.; Pettus, T. R. R., Science of Synthesis, (2007) 31, 424.
Trialkylboranes, generated in situ from borane (BH3) and a variety of substituted alkenes, add to benzo-1,4-quinone (9) in the presence of air and water to give 2-substituted benzene-1,4-diols 15 (Scheme 7).[9,10]
Meeeee 8 8,8-Meeeeeee ee Meeeeeeeeeeeeee ee Meeee-8,8-eeeeeee[88]
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8-Meeeeeeeeee Meeeeee-8,8-eeeee 88; Meeeeee Meeeeeeee:[88]
Mee eeeeee (888 eeee) ee MMM (88 eM) eee eeeee ee e eeee ee MM8 (88 eeee) ee MMM (88 eM) eeeee M8. Mee eeeeeeeee eeeeeeeeeeeeee eee eeeeeee ee 88°M eee 8 e, eee M8M (8.88 eM, 88 eeee) eee eeeee, eeeeeeee ee e eeee ee eeeee-8,8-eeeeeee (8; 88 eeee) ee MMM (88 eM). Mee eee eeee eeeeee eeeeeee eee eeeee ee e eeee ee 8 eM·eee−8. Meee eee eeeeeeee eee eeeeeeee, ee eeeeeeeee ee MM eeeeeeee (∼88 eee), eee eeeeeee eee eeeee eeeeeeeee ee eeeeee eee eeeeeee ee eeee ee eee eeeeeee eee eeeeeee eeee eeeeeeeeee. Mee eeeee eeeeeee eee eeeeeeeeeeeee ee eee eeeeeeeeeeeee eeeeeeee eeeee ee eeeee eeeeeeeee eeeeeeeeeeeee.
References
[9] | Meeeeee, M. M., M. Meeeeeeee. Meee., (8888) 88, M88. |
[10] | Meeeeee, M. M., Meeeeeeeeee, (8888) 88, 8888. |
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- 8.Meeeee-Meee, (8888) 8/8e8, 888.