Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/40106
Title: Synthesis of substituted pyrrolo- and indolo-quinoxalines via the gold(i)-catalyzed tandem hydroamination-hydroarylation of pyrrole- and indole-substituted anilines with aromatic terminal alkynes.
Authors: Koh, Chii Boon.
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2010
Abstract: A concise, asymmetric synthesis of substituted 3-pyrrolines from the corresponding amino-homoallylic alcohols derived from amino acids is described. The key step is an intramolecular hydroamination reaction catalyzed by copper(II) triflate. The 3-pyrroline products were obtained in moderate to good yields and with excellent diastereoselectivity and enantioselectivity.
URI: http://hdl.handle.net/10356/40106
Fulltext Permission: restricted
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Student Reports (FYP/IA/PA/PI)

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