Isolation and synthesis of biologically active carbazole alkaloids

HJ Knölker, KR Reddy - Chemical reviews, 2002 - ACS Publications
Carbazole 1 was isolated first from coal tar in 1872 by Graebe and Glazer (Figure 1). 1 In
1965, Chakraborty et al. described the isolation and antibiotic properties of murrayanine …

Hetero Diels-Alder reactions in organic chemistry

LF Tietze, G Kettschau - Stereoselective Heterocyclic Synthesis I, 1997 - Springer
Abstract The hetero Diels-Alder reaction is one of the most important methods for the
synthesis of heterocycles. In this article an overview is given for the period since 1989 …

Tandem Rh (III)-catalyzed C–H amination/annulation reactions: synthesis of indoloquinoline derivatives in water

L Shi, B Wang - Organic letters, 2016 - ACS Publications
An efficient Rh (III)-catalyzed synthetic method for indoloquinoline derivatives from readily
available indoles and isoxazoles was developed. This annulation procedure undergoes …

Application of iminophosphorane-based methodologies for the synthesis of natural products

PM Fresneda, P Molina - Synlett, 2004 - thieme-connect.com
Four methodologies based on the aza-Wittig reaction have been used for the preparation of
the wide variety of nitrogen-containing natural products. The synthesis of quinoline, β …

A tandem approach to functionalized carbazoles from indoles via two successive regioselective oxidative Heck reactions followed by thermal electrocyclization

JK Laha, N Dayal - Organic letters, 2015 - ACS Publications
A direct one-pot approach to the synthesis of carbazoles (mono-, di-, and trisubstituted) and
α-carbolines from readily available indoles or 7-azaindoles and alkenes is described. Based …

Synthesis of Carbocyclic and Heterocyclic Fused Quinolines by Cascade Radical Annulations of Unsaturated N-Aryl Thiocarbamates, Thioamides, and Thioureas

W Du, DP Curran - Organic letters, 2003 - ACS Publications
Tandem radical cyclizations of suitably substituted N-aryl thiocarbamates, thioamides, and
thioureas are induced by exposure to tris (trimethylsilyl) silane (TTMSH) and UV light and …

Iminophosphoranes: Versatile tools in heterocyclic synthesis

H Wamhoff, G Richardt, S Stölben - Advances in Heterocyclic Chemistry, 1995 - Elsevier
Within the last decades, the aza-Wittig reaction has assumed increasing importance for the
specific construction of many heterocyclic systems. This first comprehensive review provides …

Regioselective palladium (II)-catalyzed synthesis of five-or seven-membered ring lactones and five-, six-or seven-membered ring lactams by cyclocarbonylation …

B El Ali, K Okuro, G Vasapollo… - Journal of the American …, 1996 - ACS Publications
2-Allylphenols react with carbon monoxide and hydrogen in the presence of catalytic
quantities of a cationic palladium (II) complex [(PCy3) 2Pd (H)(H2O)]+ BF4-or palladium …

Metal-Free and Regioselective Synthesis of Functionalized α-Carbolines via [3+ 3] Annulation of Morita–Baylis–Hillman Acetates of Nitroalkenes with Iminoindolines

ST Sivanandan, INN Namboothiri - The Journal of Organic …, 2021 - ACS Publications
A facile, metal-free method for the synthesis of substituted α-carbolines from secondary
Morita–Baylis–Hillman (MBH) acetates of nitroalkenes is presented. The cascade reaction of …

Selective and efficient syntheses of perhydro-1, 3, 5-triazine-2, 4, 6-triones and carbodiimides from isocyanates using ZP (MeNCH2CH2) 3N catalysts

J Tang, T Mohan, JG Verkade - The Journal of Organic Chemistry, 1994 - ACS Publications
0, 4; Ch= S, 5) selectively catalyzethe transformation of isocyanates to carbodiimides and do
so more efficiently than their acyclic analogues 0= P (NMe2) a and (MeO) 2P (S) Ph …