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C-C bond formation in an oxidative dimerization induced by gold

C-C bond formation via direct arylation shown with a substituted thiophene and a substituted bromobenzene.

C-C bond formation via iron-catalysed benzylic C-H activation.

C-C Bond forming reactions involving the use of L2PH reagents

C-C bond forming reactions using polymer-supported phosphorus ylide

C-C bond length of adamantane and perfluoroadamantane .

C-C bond lengths and angles of some prismanes, calculated at the B3LYP 6-311G the B3LYP 6-31G levels

C-C bond-forming coupling reactirais of aryl cyanides catalyzed by rhodium

C-C bond-forming reaction through an aldol-type addition on a core

C-C coupling and pyridine dearomatization initiated by the deprotonation of a dimethylsulfide ligand.

C-C coupling between a monodentate N-RIm ligand and the pyridine ring of a pyridylimidazole chelate.

C-C coupling from malonate derivatives

C-C coupling from ylides with alcohols

C-C coupling of a variety of N-aryltetrahydroisoquinolines with nitroalkanes and dimethyl malonate over mpg-C3N4

C-C coupling of a variety of N-aryltetrahydroisoquinolmes with CH3NO2 and KCN over Ti02

C-C coupling of alkynes catalyzed by lT2 complexes

C-C coupling on a Ni complex having two propagating oligo-p-pheny-lene groups to produce PPP.

C-C coupling on Ni to produce biphenyl Ph-Ph. This type of complex is isolable when the Ph group has electron-withdrawing substituents such as -C6F5, and its molecular structure has been revealed by X-ray crystallography. bpy 2,2 -bip5ridyl.

C-C double bond cleavage of benzalacetone

C-C double bond cleavage of cyclohepten-2-one

C-C ix nd cleavage reaction in the CYP82Gl-eatalyzed formation of terpene hydrocarbons from precursor alcohols

C-C Reductive elimination from la and 3 and H-D exchange

C-C sections occurred funnels because well 3, well 7, well 12 are pumping wells with withdrawals of 350 m d, 200 m d, 1000 m d. Well 11 and well 12 located adjacent to C-C section near Luan River and here is village sewage ditch

C-C single bond distances in C4 hydrocarbons with double and triple bonds.

C-C TOCSY of C-labelled glucose.The three top panels depict expansions of the boxed spectral regions in the lower panels. The double arrows indicate selected cross-sections that belong to the a and forms of glucose. Reprinted from Zhang et al. , Copyright 2012, with permission from Elsevier.



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