Publication:
Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid: a chiral resolving agent for the resolution and absolute configuration assignment of 7,7'-disubstituted 1,1'-bi-2-naphthols

Issued Date

2016-01-01

Resource Type

Article

ISSN

1362511X
09574166

DOI

10.1016/j.tetasy.2016.09.003

Other identifier(s)

2-s2.0-84994267567

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Asymmetry. Vol.27, No.22-23 (2016), 1113-1120

Suggested Citation

Kulvadee Dolsophon, Nopporn Ruangsupapichat, Jakapun Soponpong, Suttipun Sungsuwan, Samran Prabpai, Palangpon Kongsaeree, Tienthong Thongpanchang Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid: a chiral resolving agent for the resolution and absolute configuration assignment of 7,7'-disubstituted 1,1'-bi-2-naphthols. Tetrahedron Asymmetry. Vol.27, No.22-23 (2016), 1113-1120. doi:10.1016/j.tetasy.2016.09.003 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/43340

Research Projects

Organizational Units

Authors

Journal Issue

Thesis

Title

Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid: a chiral resolving agent for the resolution and absolute configuration assignment of 7,7'-disubstituted 1,1'-bi-2-naphthols

Author(s)

Kulvadee Dolsophon
 Nopporn Ruangsupapichat
 Jakapun Soponpong
 Suttipun Sungsuwan
 Samran Prabpai
 Palangpon Kongsaeree
 Tienthong Thongpanchang

Other Contributor(s)

Mahidol University
 Thailand National Center for Genetic Engineering and Biotechnology

Abstract

© 2016 Elsevier Ltd Tetrahydro-1,4-epoxynaphthalene-1-carboxylic acid (THENA), was applied as a chiral derivatizing agent to resolve 7,7'-disubstituted 1,1'-bi-2-naphthol derivatives. This process is very efficient and could potentially be used as a preliminary tool to assign the absolute configuration of substituted 1,1'-bi-2-naphthols by means of a simple TLC.

Keyword(s)

Chemical Engineering
 Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/43340

Collections

Scopus 2016-2017