Reversing Enantioselectivity Using Noncovalent Interactions in Asymmetric Dearomatization of β-Naphthols: The Power of 3,3′ Substituents in Chiral Phosphoric Acid Catalysts

被引：34

作者：

Changotra, Avtar ^{[1
]}

Das, Sandip ^{[1
]}

Sunoj, Raghavan B. ^{[1
]}

机构：

[1] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India

来源：

ORGANIC LETTERS | 2017年 / 19卷 / 09期

关键词：

BRONSTED-ACID; RING OPENINGS; MECHANISM; STEREOSELECTIVITY; DESYMMETRIZATION; CYCLIZATION; SELECTIVITY; ACTIVATION; ORIGINS; ESTERS;

D O I：

10.1021/acs.orglett.7b00890

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The sense of enantioselectivity in asymmetric dearomative amination of beta-naphthols is reported to pivotally depend on the 3,3' substituents on the chiral BINOL- phosphoric acid (CPA) catalysts. The origin of reversal in the sense of stereoinduction from R to S, when the aryl substituent is changed from 3,5-(CF3)(2)-C6H3 (CPA-1) to 9-anthryl (CPA-2), has been identified as arising due to the change in the pattern of noncovalent interactions (from predominantly C-H center dot center dot center dot F to C-H center dot center dot center dot pi interactions) in the stereocontrolling transition states.

引用

页码：2354 / 2357

页数：4

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