Isolation and synthesis of biologically active carbazole alkaloids

The catalytic production of organic molecules is one of the most important applications of organometallic chemistry. For this purpose the distinct reaction chemistry of organic ligands covalently bound to transition metals is exploited. Most organometallic chemistry has focused on the formation of carboncarbon or carbon-hydrogen bonds. The platinum group metals, in particular Pd and Rh, have been the most commonly used elements insfrequently commercializedscatalytic processes that include hydrogenation, hydroformylation and others. On the other hand, carbon-oxygen and carbon-nitrogen bonds are found in the majority of organic molecules and are of particular importance in physiologically active substances. However, catalytic organometallic reactions that lead to the formation of carbonheteroatom bonds are less common.1,2 The catalytic construction of carbon-nitrogen bonds in amines is particularly rare.3-10 Clearly, efficient catalytic routes to nitrogen based molecules are of great interest.11 Especially useful are catalytic hydroaminations of olefins and alkynes which avoid production of byproducts, like salts, generally observed in metal-catalyzed aminations of C-X derivatives (X ) e.g., halogen). However, known aminations of olefins often require stoichiometric use of transition metals and general methods for carrying out aminations catalytically are not yet available.12,13 Most of the present enantioselective syntheses of molecules bearing an amine functionality use classical stoichiometric reactions with chiral auxiliaries or utilize enantiomerically pure starting material.14-16 Hydroamination of alkenes and alkynes, which constitutes the formal addition of a N-H bond across a carbon-carbon multiple bond (Scheme 1), is a transformation of seemingly fundamental simplicity and would appear to offer the most attractive route to numerous classes of organo-nitrogen molecules such as alkylated amines, enamines or imines. Organic chemists have developed various synthetic approaches for the amination of olefins.17-19 Direct addition of nucleophiles H-NR2 to activated alkenes is of general importance for the synthesis of compounds with nitrogen atoms â to groups such as keto, ester, nitrile, sulfoxide, or nitro.13,20-23 These additions usually lead to the anti-Markovnikov products. On the other hand aliphatic olefins as well as most aromatic olefins are often aminated to give the Markovnikov product. One possibility to reverse the reactivity of aliphatic olefins is the use of electrophilic nitrogen radicals which have been used to obtain anti-Markovnikov products.24 In the past much work has been done on the activation of alkenes with stoichiometric amounts of metal.24 Reactions are mostly promoted by complexes of titanium,25 iron,26 zirconium,27 palladium28-31 and mercury.32,33 However, catalytic additions of amines H-NR2 to nonactivated double or triple bonds are still rare. Two basic approaches have been employed to catalytically effect aminations and involve either alkene/alkyne or amine activation routes (Scheme 2).34,140 Alkene activation is generally accomplished with late-transition-metal catalysts, which render coordinated olefins more susceptible to attack by † Dedicated to Dipl. Chem. Martin Eichberger (deceased 11/20/ 1997). 675 Chem. Rev. 1998, 98, 675−703

Metal-Initiated Amination of Alkenes and Alkynes.

Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids

The structural chemistry of metal thiolate complexes

Heterocyclische Carbene – Synthese und Koordinationschemie

Uranyl complexes of acetamidoxime and benzamidoxime. Preparation, characterization, and crystal structure

Carbazole alkaloids from seeds of Murraya koenigii

Die Rontgenstrukturanalysen von S3N2+SO3CF3−− 1/2 CH3CN (1) und S3N2NSO2F (2) zeigen in 1 ein planares S3N2+-Radikalkation, wobei zwei Kationen uber schwache S-S-Wechselwirkungen zu sesselformigen Dimeren assoziiert sind. Der an einem S-Atom der S S-Gruppe substituierte S3N2-Ring in 2 ist nicht planar; die S S-Bindung ist schwacher als in 1.



Crystal and Molecular Structures of the S3N2+ Radical Cation in S3N2+SO3CF3− · 1/2 CH3CN and of S3N2(NSO2F)



The molecular and crystal structures of S3N2+SO3CF3− · 1/2 CH3CN (1) and S3N2NSO2F (2) were determined from single crystal X-ray diffraction data. The S3N2+ radical cation in 1 is planar, two cations being connected through weak SS bonding interactions to form dimers with a chair configuration. The S3N2 ring of 2, in which the NSO2F group is covalently bonded to one of the S atoms of the S S group, is not planar; the S S bond is weaker than in 1.

Kristall‐ und Molekülstrukturen des S3N‐Radikalkations in S3NSO3CF · 1/2 CH3CN und von S3N2(NSO2F)

Synthetic routes to [Fe2X2(X5)2]2− anions (X=S, Se). Structure and properties of [Fe2Se2(Se5)2]2−, a complex with selenido and pentaselenido ligands

The complete manuscript of this communication appears in: Angew. Chem. Suppl. 1983, 1176. DOI:10.1002/anie.198311760

Gerald Henkel

Papers

Uranyl complexes of acetamidoxime and benzamidoxime. Preparation, characterization, and crystal structure

Carbazole alkaloids from seeds of Murraya koenigii

Kristall‐ und Molekülstrukturen des S3N‐Radikalkations in S3NSO3CF · 1/2 CH3CN und von S3N2(NSO2F)

Synthetic routes to [Fe2X2(X5)2]2− anions (X=S, Se). Structure and properties of [Fe2Se2(Se5)2]2−, a complex with selenido and pentaselenido ligands

[Ph4P]2[V2(SC2H4S)4]·4MeOH: The First Polynuclear Vanadium‐Sulfur Complex with Pure Sulfur Coordination