Literature DB >> 22146671

Cl-BODIPYs: a BODIPY class enabling facile B-substitution.

Travis Lundrigan1, Sarah M Crawford, T Stanley Cameron, Alison Thompson.   

Abstract

Cl-BODIPYs, synthesized in high yields from dipyrrins under air- and moisture-free conditions, are extremely facile to substitution at boron compared to their corresponding F-BODIPYs, opening up a new route to BODIPYs functionalized at boron. This journal is © The Royal Society of Chemistry 2012

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22146671     DOI: 10.1039/c1cc16351e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Stability of a Series of BODIPYs in Acidic Conditions: An Experimental and Computational Study into the Role of the Substituents at Boron.

Authors:  Maodie Wang; M Graça H Vicente; Deanna Mason; Petia Bobadova-Parvanova
Journal:  ACS Omega       Date:  2018-05-21

2.  Syntheses and Investigations of Conformationally Restricted, Linker-Free α-Amino Acid-BODIPYs via Boron Functionalization.

Authors:  Maodie Wang; Guanyu Zhang; Petia Bobadova-Parvanova; Kevin M Smith; M Graça H Vicente
Journal:  J Org Chem       Date:  2021-11-22       Impact factor: 4.354

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.