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  2. 9-Borabicyclo (3.3.1)nonane - Wikipedia

    en.wikipedia.org/wiki/9-Borabicyclo(3.3.1)nonane

    9-Borabicyclo[3.3.1]nonane or 9-BBN is an organoborane compound. This colourless solid is used in organic chemistry as a hydroboration reagent. The compound exists as a hydride-bridged dimer, which easily cleaves in the presence of reducible substrates. [1] 9-BBN is also known by its nickname 'banana borane'. [2]

  3. Alpine borane - Wikipedia

    en.wikipedia.org/wiki/Alpine_borane

    This reagent is generated by treating 9-BBN with α-pinene. [2]This sterically crowded chiral trialkylborane can stereoselectively reduce aldehydes in what is known as the Midland Alpine borane reduction, or simply the Midland reduction.

  4. Borylation - Wikipedia

    en.wikipedia.org/wiki/Borylation

    In the same year, M. M. Midland discovered B-3-alpha-pinanyl-9-BBN as the reducing agent, which could be easily available by reacting (+)-alpha-pinene with 9-BBN. The new reducing agent was later commercialized by Aldrich Co. under the name Alpine Borane and the asymmetric reduction of carbonyl groups with either enantiomer of Alpine-Borane is ...

  5. BBN - Wikipedia

    en.wikipedia.org/wiki/BBN

    9-Borabicyclo(3.3.1)nonane (9-BBN), a reagent used in organic chemistry; The 3-letter code for Blackburn railway station in the UK; Blackburn railway station, Melbourne; Bengbu South railway station, China Railway pinyin code BBN; Raytheon BBN Technologies, formerly Bolt, Beranek and Newman, a technology company in Cambridge, Massachusetts

  6. File:9-BBN dimer structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:9-BBN_dimer_structure.svg

    9-硼二环[3.3.1]壬烷 Metadata This file contains additional information, probably added from the digital camera or scanner used to create or digitize it.

  7. Catecholborane - Wikipedia

    en.wikipedia.org/wiki/Catecholborane

    C 6 H 4 O 2 BH + HC 2 R → C 6 H 4 O 2 B-CHCHR. The product is a precursor to the Suzuki reaction and is the only borane which stops at the alkene instead of reacting further to the alkane. [3] [4] Catecholborane may be used as a stereoselective reducing agent when converting β-hydroxy ketones to syn 1,3-diols.

  8. B3 domain - Wikipedia

    en.wikipedia.org/wiki/B3_domain

    The B3 DNA binding domain (DBD) is a highly conserved domain found exclusively in transcription factors (≥40 species) (Pfam PF02362) combined with other domains (InterPro: IPR003340). It consists of 100-120 residues, includes seven beta strands and two alpha helices that form a DNA-binding pseudobarrel protein fold ( SCOP 117343 ); it ...

  9. Disiamylborane - Wikipedia

    en.wikipedia.org/wiki/Disiamylborane

    Disiamylborane (bis(1,2-dimethylpropyl)borane) is an organoborane with the formula [((CH 3) 2 CHCH(CH 3)) 2 BH] 2 (abbreviation: Sia 2 BH). It is a colorless waxy solid that is used in organic synthesis for hydroboration–oxidation reactions. Like most dialkyl boron hydrides, it has a dimeric structure with bridging hydrides.