Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About
0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | a | b | c | d | e | f | g | h | i | j | k | l | m | n | o | p | q | r | s | t | u | v | w | x | y | z

   |<      <<      >>     > |    


Macrocyclisation equilibrium constants for polydimethylsiloxane. Experimental data are shown as dashed curves as follows

Macrocyclisation for the xestocyclamine A synthesis.

Macrocyclisations of 2-iodobenzamides bearing allyloxy groups in their side chains

Macrocyclization achieved on a solid support. A

Macrocyclization achieved on a solid support. A Pd2, PPh , Bu4NC1, DMF EtjN water 9

Macrocyclization achieved on a solid support. A PdCOAc , PPh, Bu NCl, DMF EtjN water 9

Macrocyclization by 1,3-dipolar cycloaddition

Macrocyclization by RCM in Fiirstner s total synthesis of the resin glycoside woodrosin I

Macrocyclization by RCM in the total synthesis of the antifungal antibiotic PF1163B

Macrocyclization exploiting amination of pyridine iV-oxides

Macrocyclization in polymerization of THF initiated with strong protonic acids. The suspension points denote a number of repeating units .

Macrocyclization in the synthesis of a catenane and rotaxane reported by Stoddart and coworkers.

Macrocyclization is obtained by controlled addition of pyridine solutions of the resulting oligothiophenes to a slurry of anhydrous CuCl and CuC in pyridine at RT step c in Fig.

Macrocyclization of a symmetrical porphyrazine.

Macrocyclization of peptides by click chemistry between propargylic acid residues and an azide- functionalized amino acid

Macrocyclization of the relay-armed RRCM substrate 128 occurring via direct RCM en route to the bryostatin analog 131.

Macrocyclization of ynals

Macrocyclization on a solid phase.

Macrocyclization on the SynPhase surface.

Macrocyclization reactions applied in epothilone total syntheses. From top to bottom

Macrocyclization reactions to form strained paracyclophanes.

Macrocyclization through intramolecular reductive coupling.

Macrocyclization through nitrenium ion arene couphng.

Macrocyclization to form 14-membered macrolactones.

Macrocyclization to form a 10-membered, macrocyclic ketone.



   |<      <<      >>     > |    

SEARCH



© 2024 chempedia.info