SYNTHESIS OF THIOPHENE OLIGOMERS VIA ORGANOTIN COMPOUNDS
β Scribed by Al-taweel, Samir A.; Al-saraierh, Hassan F.
- Book ID
- 121191555
- Publisher
- Taylor and Francis Group
- Year
- 1999
- Tongue
- English
- Weight
- 449 KB
- Volume
- 155
- Category
- Article
- ISSN
- 1042-6507
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π SIMILAR VOLUMES
Oligomers containing from 2 to 6 thiophene units attached by their 2 and 5 positions were synthesized unambiguously by iodine oxidation of a suitable ate complex obtained by stepwise reactions of 9-BBN with methanol, a 2\_lithiothiophene, boron trifluoride etherate, and a second 2-lithiothiophene. T
9-borabicyclo [3.3.1]nonane, A Commercially Available Reagent, Is The Most Versatile Hydroborating Reagent To Synthesize Organoboranes (b-r-9-bbn). The Reagent Exhibits Remarkable Regio-, Chemo-, And Stereoselectivity During Hydroboration Reactions. The Organoboranes Can Be Converted To C-h, C-o, C-