Metal-Catalyzed N-H and O-H Insertion from alpha-Diazocarbonyl Compounds

By (author) Yuling Hu

Extent: 208, 208 pages

Publisher: Logos Verlag Berlin

Subjects: Earth & Life Sciences

Series: Beiträge zur organischen Synthese

Series volume number: 79

Language: English

Paperback (Published)

(March 2019)

ISBN: 9783832548643

5.71 x 8.27 inches

Price: $71.00

Out of stock

Synopsis
Contributing Authors

Transition-metal catalyzed X-H insertions from alpha-diazocarbonyl compounds represent one of the most efficient approaches to form C–X bonds. The presented thesis is based on the synthesis and application of alpha-diazocarbonyl compounds in metal-catalyzed N-H insertion and the chemoenzymatic synthesis of heterocycles via a [Cu]/[Rh] catalyzed intramolecular O-H insertion. In the first part, a straightforward approach via the Wittig reaction, gamma-Umpolung addition and diazo transfer reaction allowed the synthesis of unsaturated alpha-diazocarbonyl compounds with ease. In the second part, the newly synthesized (R textsubscript{p)-pseudo-ortho [2.2]paracyclophane-based bisoxazoline ligands presented superior reactivity. The obtained delta-amino alpha,beta-unsaturated carboxylic esters were used to synthesize hexahydroindoles, which are key intermediates in the synthesis route of Rostratin B-D. Additional investigation of alpha-diazocarbonyl compounds led to the enzymatic synthesis of O-Heterocycles. With the employment of enantiopure starting material obtained from ketoreductase LbADH, the enantioselectivity of each diastereomer from the O-H insertion product have been effectivity improved.

By (author) Yuling Hu

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