Authors

Chih-Wei Chien

Type

Text

Type

Dissertation

Advisor

Kerber, Robert | Ojima, Iwao | Goroff, Nancy | Gupta, Ramesh.

Date

2013-12-01

Keywords

Chemistry | allocolchicinoid, asymmetric synthesis, biphenol-based phosphorus ligand, colchicinoid, rhodium-catalyzed cycloaddition

Department

Department of Chemistry.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/77104

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Chiral ligand design is crucial for the asymmetric transformations. In our laboratory, libraries of fine-tunable phosphorus ligands based on axially chiral biphenol have been well developed. These ligands exhibit excellent enantioselectivity in various transition-metal catalyzed asymmetric reactions. We present here the application of the monodentate phosphoramidite (MPN) ligand library to the Pd-catalyzed intramolecular asymmetric allylic amination (AAA) for the formation of chiral 1-vinyltetrahydroiso-quinoline skeleton, a versatile key intermediate in the synthesis of natural products such as isopyruthaline and (− )-O-methylthaicanine. We also studied the Pd-catalyzed inter-molecular AAA reaction using our bidentate diphosphonite (BOP) ligands. The BOP ligands exhibit excellent efficacy in this reaction, which provides a key intermediate for the total synthesis of Strychnos indole alkaloids. The non-benzenoid aromatics, tropones and tropolones, are found in various natural products such as colchicine and hinokitol, which possess significant biological activities. The traditional methods to construct the tropone skeletons include oxidation of cycloheptatriene and [4+3] cycloadditions. In addition, the total synthesis of colchicine and its analogues requires laborious organic transformations in the formation of 6-7-7 fused rings systems. Transition metal-catalyzed carbocyclization and cycloaddition reactions have proven to be among the most efficient methods for constructing complex polycyclic systems. Rh-catalyzed carbocyclizations (i.e. SiCaC, SiCaT, CO-SiCaT) and higher order cycloaddition reactions can give novel fused-cyclic products. We present here the application of Rh-catalyzed [2+2+2+1] cycloaddition to the one-step formation of the 6-7-7-5 fused-tetracyclic scaffold of colchicinoids. Furthermore, a microwave-mediated Rh-catalyzed [2+2+2] cycloaddition to synthesize the allocolchicinoids was developed as well. | 327 pages

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