Intramolecular cyclization of C2 symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars

Sung Ho Kang; Do Hyun Ryu

doi:10.1016/S0040-4039(96)02403-3

Intramolecular cyclization of C₂ symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars

Sung Ho Kang
, Do Hyun Ryu

Korea Advanced Institute of Science and Technology

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

21 Scopus citations

Abstract

C₂ Symmetric and meso-iodo hydroxy ammonium chlorides generated from 2 and 5 have been cyclized under basic conditions to produce various heterocycles chemoselectively, which comprise tetrahydrofurans 7 and 19, piperidines 13, 15 and 2, and pyrrolidines 17 and 18.

Original language	English
Pages (from-to)	607-610
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	4
DOIs	https://doi.org/10.1016/S0040-4039(96)02403-3
State	Published - 27 Jan 1997
Externally published	Yes

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@article{c691ecb191ed44078aed0bd56048fa56,

title = "Intramolecular cyclization of C2 symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars",

abstract = "C2 Symmetric and meso-iodo hydroxy ammonium chlorides generated from 2 and 5 have been cyclized under basic conditions to produce various heterocycles chemoselectively, which comprise tetrahydrofurans 7 and 19, piperidines 13, 15 and 2, and pyrrolidines 17 and 18.",

author = "Kang, \{Sung Ho\} and Ryu, \{Do Hyun\}",

year = "1997",

month = jan,

day = "27",

doi = "10.1016/S0040-4039(96)02403-3",

language = "English",

volume = "38",

pages = "607--610",

journal = "Tetrahedron Letters",

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number = "4",

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TY - JOUR

T1 - Intramolecular cyclization of C2 symmetric and meso-iodo amino alcohols

T2 - A synthetic approach to azasugars

AU - Kang, Sung Ho

AU - Ryu, Do Hyun

PY - 1997/1/27

Y1 - 1997/1/27

N2 - C2 Symmetric and meso-iodo hydroxy ammonium chlorides generated from 2 and 5 have been cyclized under basic conditions to produce various heterocycles chemoselectively, which comprise tetrahydrofurans 7 and 19, piperidines 13, 15 and 2, and pyrrolidines 17 and 18.

AB - C2 Symmetric and meso-iodo hydroxy ammonium chlorides generated from 2 and 5 have been cyclized under basic conditions to produce various heterocycles chemoselectively, which comprise tetrahydrofurans 7 and 19, piperidines 13, 15 and 2, and pyrrolidines 17 and 18.

UR - https://www.scopus.com/pages/publications/0031023039

U2 - 10.1016/S0040-4039(96)02403-3

DO - 10.1016/S0040-4039(96)02403-3

M3 - Article

AN - SCOPUS:0031023039

SN - 0040-4039

VL - 38

SP - 607

EP - 610

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 4

ER -

Intramolecular cyclization of C₂ symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars

Abstract

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