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Key Documents

Autres documents

637998

Sigma-Aldrich

Vinylboronic anhydride pyridine complex

95%

Synonyme(s) :

2,4,6-Trivinylcyclotriboroxane pyridine complex, Trivinyl-boroxin pyridine complex, Trivinylcyclotriboroxane pyridine complex

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About This Item

Formule empirique (notation de Hill):
C6H9B3O3 · C5H5N
Numéro CAS:
442850-89-7
Poids moléculaire :
240.67
Numéro MDL:
MFCD03839940
Code UNSPSC :
12352103
ID de substance PubChem :
24882902
Nomenclature NACRES :
NA.22

Niveau de qualité

100

Pureté

95%

Forme

solid

Température de stockage

−20°C

Chaîne SMILES 

c1ccncc1.C=Cb2ob(C=C)ob(C=C)o2

InChI

1S/C6H9B3O3.C5H5N/c1-4-7-10-8(5-2)12-9(6-3)11-7;1-2-4-6-5-3-1/h4-6H,1-3H2;1-5H

Clé InChI

YLHJACXHRQQNQR-UHFFFAOYSA-N

Application

Reagent used for
  • Suzuki-Miyaura cross-coupling
  • Stereoselective synthesis via Palladium-catalyzed carboamination
  • Alkyl-connected 2-amino-6-vinylpurine (AVP) crosslinking agent to cytosine base in RNA
  • Kaiser oxime resin-derived palladacycle as a recoverable polymeric precatalyst in Suzuki-Miyaura cross-coupling reactions in aqueous media
  • Kinetic resolution of phosphoryl and sulfonyl esters of binaphthol derivatives via Pd-catalyzed alcoholysis of their vinyl ethers
  • Stereoselective isomerization of N-allyl aziridines into Z-enamines by using rhodium hydride catalysis
  • Kinetic resolution of axially chiral biaryl derivatives via palladium/chiral diamine ligand-catalyzed alcoholysis
  • Transition metal-catalyzed alkenylation of aziridines, cycloaddition and thermal rearrangement reactions
  • Intramolecular Heck reaction strategy for synthesis of functionalized tetrahydroanthracenes

Reagent used for Preparation of
  • BACE-1 inhibitors and SAR of cyclic sulfone hydroxyethylamines
  • Distorted spiropentanes
  • Small molecule bradykinin B2 receptor antagonists in angioedema therapy
  • Enol Ethers
  • Styryl cyclobutanone

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H319

Conseils de prudence

P305 + P351 + P338

Classification des risques

Eye Irrit. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

176.0 °F - closed cup

Point d'éclair (°C)

80 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Kuan-Jen Su et al.
The Journal of organic chemistry, 75(21), 7494-7497 (2010-10-14)
Tetravinylbenzene 4 was prepared in nearly quantitative yield from commercially available tetrabromobenzene; the improved, one-step procedure now employs Suzuki-Miyaura cross-coupling conditions. Intermolecular cyclopropanation of 4 with dibromocarbene gave a series of gem-dibromide adducts. Intramolecular cyclopropanation of monoadduct 5, putatively by
Masahiro Murakami et al.
Organic letters, 7(10), 2059-2061 (2005-05-07)
Two structurally distinct carbocycles were selectively obtained by the reactions of 2-(o-styryl)cyclobutanones promoted by ytterbium salts. Treatment of the cyclobutanones with YbCl(3) in 1,4-dioxane at 100 degrees C afforded 2-(2-chloroethyl)naphthalenes. On the other hand, the reaction with Yb(OTf)(3) in chlorobenzene
Product subclass 3: enol ethers
Milata, V.; Radl, S.; Voltrova, S.
Sci. Synth., 32, 589-756 (2008)
Derek S Tsang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(3), 886-894 (2007-11-10)
In the presence of rhodium(I) hydride catalysts, tertiary N-allylamines are known to isomerise into E enamines. In contrast, we have recently found that N-allylaziridines isomerise to form Z enamines. On the basis of literature data, the most likely mechanism of
Kinetic resolution of phosphoryl and sulfonyl esters of 1,1'-bi-2-naphthol via Pd-catalyzed alcoholysis of their vinyl ethers
Sakuma, T.; et al.
Tetrahedron, 19, 1593-1599 (2008)
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