Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine

Jung Youl Park; Choul Hong Park; Isao Kadota; Yoshinori Yamamoto

doi:10.1016/S0040-4039(97)10866-8

Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine

Jung Youl Park, Choul Hong Park, Isao Kadota, Yoshinori Yamamoto

Research output: Contribution to journal › Article › peer-review

20 Citations (Scopus)

Abstract

The Lewis acid mediated cyclization of γ-oxygen substituted allylic stannane 1, having a chiral imine group at the terminus of the carbon chain, afforded trans-β-amino cyclic ether 2 with very high to good diastereoselectivities in high chemical yields.

Original language	English
Pages (from-to)	1791-1794
Number of pages	4
Journal	Tetrahedron Letters
Volume	39
Issue number	13
DOIs	https://doi.org/10.1016/S0040-4039(97)10866-8
Publication status	Published - Mar 26 1998
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(97)10866-8

Cite this

@article{d3977306962d412daa703e55ef1be814,

title = "Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine",

abstract = "The Lewis acid mediated cyclization of γ-oxygen substituted allylic stannane 1, having a chiral imine group at the terminus of the carbon chain, afforded trans-β-amino cyclic ether 2 with very high to good diastereoselectivities in high chemical yields.",

author = "Park, {Jung Youl} and Park, {Choul Hong} and Isao Kadota and Yoshinori Yamamoto",

year = "1998",

month = mar,

day = "26",

doi = "10.1016/S0040-4039(97)10866-8",

language = "English",

volume = "39",

pages = "1791--1794",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "13",

}

TY - JOUR

T1 - Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine

AU - Park, Jung Youl

AU - Park, Choul Hong

AU - Kadota, Isao

AU - Yamamoto, Yoshinori

PY - 1998/3/26

Y1 - 1998/3/26

N2 - The Lewis acid mediated cyclization of γ-oxygen substituted allylic stannane 1, having a chiral imine group at the terminus of the carbon chain, afforded trans-β-amino cyclic ether 2 with very high to good diastereoselectivities in high chemical yields.

AB - The Lewis acid mediated cyclization of γ-oxygen substituted allylic stannane 1, having a chiral imine group at the terminus of the carbon chain, afforded trans-β-amino cyclic ether 2 with very high to good diastereoselectivities in high chemical yields.

UR - http://www.scopus.com/inward/record.url?scp=0032568220&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032568220&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)10866-8

DO - 10.1016/S0040-4039(97)10866-8

M3 - Article

AN - SCOPUS:0032568220

SN - 0040-4039

VL - 39

SP - 1791

EP - 1794

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 13

ER -

Asymmetric synthesis of β-amino cyclic ethers via the intramolecular reaction of γ-alkoxyallylstannane with chiral imine

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this