pinacolato | Bis(pinacolato)diboron

Keyword	CPC	PCC	Volume	Score	Length of keyword
pinacolato	0.76	0.8	6167	93	10

Keyword	CPC	PCC	Volume	Score
pinacolato	1.1	0.7	4495	54
pinacolato diboron	1.34	0.3	7183	68
pinacolato boron	1.57	0.2	2024	100
pinacolatoboryl	0.52	0.4	7665	56
pinacolatoborate	0.13	0.2	8613	99
pinacolato drink	1.87	0.9	3127	66
pinacolato borane	1.04	0.2	9432	47
pina colada cocktail	1.06	0.7	1534	66
bis pinacolato diboron	1.02	0.6	1175	59
bis pinacolato diboron cas no	1.61	1	8798	10
bis pinacolato diboron molecular weight	1.43	1	5656	29
bis pinacolato diboron cas	0.7	0.2	618	15
bis pinacolato diboron cas no and msds	0.58	0.6	2287	93
bis pinacolato diboron cas no and properties	0.22	1	2606	94
bis pinacolato diboron cas no and safety data	0.61	0.7	9747	19
bis pinacolato diboron cas no and solubility	1.14	0.4	3605	70

Search Results related to pinacolato on Search Engine

Bis(pinacolato)diboron - Wikipedia
wikipedia.org

https://en.m.wikipedia.org/wiki/Bis(pinacolato)diboron

WEBBis(pinacolato)diboron is a covalent compound containing two boron atoms and two pinacolato ligands. It has the formula [(CH 3) 4 C 2 O 2 B] 2; the pinacol groups are sometimes abbreviated as "pin", so the structure is sometimes represented as B 2 pin 2. It is a colourless solid that is soluble in organic solvents.

DA: 18 PA: 25 MOZ Rank: 75

Bis(pinacolato)diborane | C12H24B2O4 | CID 2733548 - PubChem
nih.gov

https://pubchem.ncbi.nlm.nih.gov/compound/Bis_pinacolato_diborane

WEBBis (pinacolato)diboron is a 1,3,2-dioxaborolane that is 4,4,5,5-tetramethyl-1,3,2-dioxaborolane in which the boron hydrogen at position 2 is replaced by a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group. It is a reagent used in organic synthesis to synthesise pinacol boronic esters.

DA: 18 PA: 50 MOZ Rank: 70

Bis(pinacolato)diboron 99 73183-34-3 - MilliporeSigma
sigmaaldrich.com

https://www.sigmaaldrich.com/IN/en/product/aldrich/473294

WEBBis(pinacolato)diboron or (B 2 pin 2) is the most commonly used diborane reagent in organic synthesis due to its high stability in air and moisture. It can be synthesized by treating tetrakis(dimethylamino)diboron with pinacol in acidic conditions.

DA: 7 PA: 97 MOZ Rank: 23

Bis(pinacolato)diboron, 98+%, Thermo Scientific Chemicals - Fisher Sci
fishersci.com

https://www.fishersci.com/shop/products/bis-pinacolato-diboron-98-thermo-scientific-1/AAL1608803

WEBBis (pinacolato)diboron is a reagent used for the cis-vicinal diborylation of acetylenes and olefins with platinum catalysis. It acts as a substrate used in a new palladium-catalyzed cyclization of 1,6-enynes leading to homoallylic alkylboronates.

DA: 21 PA: 64 MOZ Rank: 17

Bis(pinacolato)diboron | 73183-34-3 - ChemicalBook
chemicalbook.com

https://www.chemicalbook.com/ChemicalProductProperty_EN_CB4306719.htm

WEBApr 8, 2024 · Definition. Bis (pinacolato)diboron is a covalent compound containing two boron atoms and two pinacolato ligands. It has the formula [ (CH3)4C2O2B]2; the pinacol groups are sometimes abbreviated as "pin", so the structure is sometimes represented as B2pin2. Uses. It is a colourless solid that is soluble in organic solvents.

DA: 82 PA: 79 MOZ Rank: 26

Bis(pinacolato)diboron, B2pin2 - Organic Chemistry Portal
organic-chemistry.org

https://www.organic-chemistry.org/chemicals/reductions/bis(pinacolato)diboron-B2pin2.shtm

WEBAn unprecedented nickel-catalyzed reductive borylation of enaminones provides β-ketone boronic esters via a challenging transformation of an alkenyl C (sp 2 )-N bond. While B 2 pin 2 plays a dual role in this process, water serves as the hydrogen source.

DA: 73 PA: 30 MOZ Rank: 52

Diastereo- and Enantioselective Reactions of Bis(pinacolato…
acs.org

https://pubs.acs.org/doi/10.1021/ja5071202

WEBAug 4, 2014 · Catalytic enantioselective multicomponent processes involving bis (pinacolato)diboron [B 2 (pin) 2 ], 1,3-enynes, and aldehydes are disclosed; the resulting compounds contain a primary C–B (pin) bond, as well as alkyne- and hydroxyl-substituted tertiary carbon stereogenic centers.

DA: 5 PA: 46 MOZ Rank: 82

Palladium-Catalyzed Cross-Coupling Reaction of Bis(pinacolato…
acs.org

https://pubs.acs.org/doi/10.1021/ja0202255

WEBJun 17, 2002 · A Broadly Applicable NHC–Cu-Catalyzed Approach for Efficient, Site-, and Enantioselective Coupling of Readily Accessible (Pinacolato)alkenylboron Compounds to Allylic Phosphates and Applications to Natural Product Synthesis.

DA: 43 PA: 92 MOZ Rank: 17

Synthesis of pinacol arylboronates via cross-coupling
sciencedirect.com

https://www.sciencedirect.com/science/article/pii/S004040200100998X

WEBDec 3, 2001 · The cross-coupling reaction between tetra (alkoxo)diborons and aryl halides or triflates in the presence of a base and PdCl 2 (dppf) provides a convenient and direct method for the synthesis of arylboronates from aryl electrophiles. 1 The coupling reaction is feasible with various functional groups, e.g. CO 2 Me, COMe, NO 2, …

DA: 20 PA: 54 MOZ Rank: 78

Bis(Pinacolato)Diboron - Ishiyama - Wiley Online Library
wiley.com

https://onlinelibrary.wiley.com/doi/abs/10.1002/0471264180.os077.18

WEBApr 28, 2003 · Abstract. Bis (pinacolato)diboron. reactant: 218 g (4.84 mol) of dimethylamine. intermediate: tris (dimethylamino)borane. intermediate: bromobis (dimethylamino)borane. intermediate: tetrakis (dimethylamino)diboron. product: Bis (pinacolato)diboron.

DA: 28 PA: 6 MOZ Rank: 91