A Convenient, One-Step Synthesis of Optically Active Tertiary Aminonaphthol and Its Applications in the Highly Enantioselective Alkenylations of Aldehydes-Reference-Cited by-同舟云学术

A Convenient, One-Step Synthesis of Optically Active Tertiary Aminonaphthol and Its Applications in the Highly Enantioselective Alkenylations of Aldehydes

Published:2003-01-23 Issue:4 Volume:68 Page:1589-1590
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ji Jian-Xin¹,Qiu Li-Qin¹,Yip Chiu Wing¹,Chan Albert S. C.¹

Affiliation:

1. Open Laboratory of Chirotechnology of the Institute of Molecular Technology for Drug Discovery and Synthesis and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China bcachan@polyu.edu.hk

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo026551k

Reference12 articles.

1. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification

2. Enantioselective addition of organozinc reagents to aldehydes

3. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds

4. Total Synthesis of (−)-Bafilomycin A1

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