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The Carbodiimide Method

1979
Publisher Summary This chapter discusses the mechanism of the carbodiimide method. The carbodiimide method was introduced to peptide synthesis with the use of dicyclohexylcarbodiimide (DCC) to affect dehydration and peptide bond formation. The procedure consisting of adding DCC to a solution of the N -protected amino acid and amino acid or peptide ...
DANIEL H. RICH, JASBIR SINGH
openaire   +1 more source

Magnesium Catalysis for the Hydroboration of Carbodiimides

Chemistry – A European Journal, 2016
AbstractA β‐diketiminato magnesium alkyl complex, [CH{C(Me)NDipp}2}MgnBu] (Dipp=2,6‐iPr2C6H3), was shown to be an effective pre‐catalyst for the first reported catalytic hydroboration of alkyl‐ and aryl‐substituted carbodiimides with pinacol borane (HBpin).
Catherine, Weetman   +2 more
openaire   +2 more sources

Cross-Linking of Gelatin with Carbodiimides

Tissue Engineering, 1996
Carbodiimides were employed for cross-linking of gelatin through amide bond formation to avoid any foreign bond incorporation into the cross-linked gelatin molecules. Cross-linking of gelatin was performed not in aqueous solution but in the form of a film under a heterogenous condition. Ethanol-water mixtures were used as the reaction medium to prevent
K, Tomihata, Y, Ikada
openaire   +2 more sources

Computational Studies of Carbodiimide Rings

The Journal of Organic Chemistry, 2014
Computational studies of alicyclic carbodiimides (RN═C═NR) (rings five through twelve) at the MP2/6-31G(d,p)//MP2/6-31G(d,p) level of theory were conducted to locate the transition states between carbodiimides isomers. Transition states for rings six through twelve were found. The RNCNR dihedral angle is ∼0° for even-numbered rings, but deviates from 0°
Robert, Damrauer   +2 more
openaire   +2 more sources

Organoactinide‐Catalyzed Monohydroboration of Carbodiimides

Chemistry – A European Journal, 2018
AbstractThe organoactinide‐catalyzed monohydroboration of carbodiimides is reported herein. The catalytic reactions proceed under very mild conditions in a highly atom‐efficient and highly selective fashion to afford the corresponding monohydroborated N‐borylformamidine products in high yields.
Heng Liu   +3 more
openaire   +2 more sources

Contact allergy to dicyclohexyl carbodiimide and diisopropyl carbodiimide

Contact Dermatitis, 1995
N, Poesen   +3 more
openaire   +2 more sources

Carbodiimides

2005
S. Braverman, M. Cherkinsky, M. L. Birsa
openaire   +2 more sources

Bis(trimethylsilyl)carbodiimide

Angewandte Chemie International Edition in English, 1962
J. Pump, U. Wannagat
openaire   +1 more source

Dicyclohexyl carbodiimide sensitivity

Contact Dermatitis, 1979
I R, White, D M, MacDonald
openaire   +2 more sources

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