Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence

Young Keun Yang, Jung Hoon Choi, Jinsung Tae

Research output: Contribution to journalArticle

40 Citations (Scopus)

Abstract

An efficient method for the synthesis of 2,3- and 2,3,4-substituted furans starting from acyclic enynes was developed using an enyne-RCM/Diels-Alder reaction sequence. The reaction conditions for the transformation of 1,2-dioxines having an adjacent 1,2-oxazine ring into furans and the cleavage of N-O bonds are discussed.

Original languageEnglish
Pages (from-to)6995-6998
Number of pages4
JournalJournal of Organic Chemistry
Volume70
Issue number17
DOIs
Publication statusPublished - 2005 Aug 19

Fingerprint

Furans
Oxazines

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

@article{acdc2c454ead447b875505a6f35b6136,
title = "Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence",
abstract = "An efficient method for the synthesis of 2,3- and 2,3,4-substituted furans starting from acyclic enynes was developed using an enyne-RCM/Diels-Alder reaction sequence. The reaction conditions for the transformation of 1,2-dioxines having an adjacent 1,2-oxazine ring into furans and the cleavage of N-O bonds are discussed.",
author = "Yang, {Young Keun} and Choi, {Jung Hoon} and Jinsung Tae",
year = "2005",
month = "8",
day = "19",
doi = "10.1021/jo050957q",
language = "English",
volume = "70",
pages = "6995--6998",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "17",

}

Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence. / Yang, Young Keun; Choi, Jung Hoon; Tae, Jinsung.

In: Journal of Organic Chemistry, Vol. 70, No. 17, 19.08.2005, p. 6995-6998.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence

AU - Yang, Young Keun

AU - Choi, Jung Hoon

AU - Tae, Jinsung

PY - 2005/8/19

Y1 - 2005/8/19

N2 - An efficient method for the synthesis of 2,3- and 2,3,4-substituted furans starting from acyclic enynes was developed using an enyne-RCM/Diels-Alder reaction sequence. The reaction conditions for the transformation of 1,2-dioxines having an adjacent 1,2-oxazine ring into furans and the cleavage of N-O bonds are discussed.

AB - An efficient method for the synthesis of 2,3- and 2,3,4-substituted furans starting from acyclic enynes was developed using an enyne-RCM/Diels-Alder reaction sequence. The reaction conditions for the transformation of 1,2-dioxines having an adjacent 1,2-oxazine ring into furans and the cleavage of N-O bonds are discussed.

UR - http://www.scopus.com/inward/record.url?scp=23644457151&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=23644457151&partnerID=8YFLogxK

U2 - 10.1021/jo050957q

DO - 10.1021/jo050957q

M3 - Article

VL - 70

SP - 6995

EP - 6998

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 17

ER -