Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hiroyoshi Noguchi"'
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry. 48:898-904
Optically active chiral organonickel complexes served as efficient chiral initiators for living aromatizing polymerization of 1,2-diisocyanobenzene derivatives, which afford optically active helical poly(quinoxaline-2,3-diyl)s up to 84% s.e. (screw-s
Publikováno v:
Organic Letters. 10:377-380
On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boron-substituted oligoarenes. The modules, i.e., monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo
Publikováno v:
Bulletin of the Chemical Society of Japan. 78:323-326
Five-membered cyclic silylboranes, 2-(diisopropylamino)-1,1-diorgano-1-sila-2-boracyclopentanes, were synthesized via intramolecular reductive B–Si bond formation with 3-[chloro(diisopropylamino)bo...
Publikováno v:
ChemInform. 39
On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boron-substituted oligoarenes. The modules, i.e., monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo
Publikováno v:
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. 129(4):758-759
The iterative synthesis of oligoarenes via an organoborane-based cross-coupling reaction (i.e., the Suzuki−Miyaura coupling) has been achieved by using a series of “masked” haloarylboronic acids as building blocks whose ordinarily reactive boro
Publikováno v:
CHEMISTRY LETTERS. 36(8):1036-1037
Oligo(quinoline-2,3-diyl)s having a terminal bromo group were synthesized by the Suzuki–Miyaura coupling of 5,8-disubstituted 2-bromoquinolin-3-ylboronic acid derivatives, and their helical structu...
Publikováno v:
Synfacts. 2007:0385-0385
Publikováno v:
Organic Letters; Feb2008, Vol. 10 Issue 3, p377-380, 4p