An Intramolecular 1,3-Dipolar Cycloaddition/Electrophilic Cyclization Sequence To Give Cyclic Ethers

DOI: 10.1021/jo00078a003

Source and publish data:

Journal of Organic Chemistry p. 7320 - 7321 (1993)

Update date:2022-08-04

Topics:

Authors:

Beebe, Xenia

Chippari, Cynthia L.

Kurth, Mark J.

Schore, Neil E.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jo00078a003

An intramolecular 1,3-dipolar cycloaddition/electrophilic cyclization sequence has been developed for the synthesis of cyclic ethers.This approach utilizes a diastereoselective nitrile oxide 1,3-dipolar cycloaddition to give furoisoxazoles, which undergo

Full text of DOI:10.1021/jo00078a003

Products guided by the article

Product name:1-phenyl-2,6-heptadien-1-ol

Cas No:148531-98-0

R&D Labs maybe for 148531-98-0

NINGXIA DARONG CHEMICALS & METALLURGY CO.,LTD.

Contact:86-952-2179751

Address:Darong Road, Dawukou, Shizuishan, Ningxia 753001, China
Jiangxi Hito Chemical Co., Ltd.

Contact:+86-792-3170318

Address:No. 6, Tianhong Ave., Xinghuo Industry Park, Yongxiu, Jiujiang, Jiangxi, China
Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
GBXF SILICONES CO.,LTD

website:http://www.gbxfsilicones.com/

Contact:86-25-68900673

Address:He Country Provincial Fine Chemical Industrial Park of Chaohu city,Anhui province,China
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou

Relevant to this article

Synthesis and aldose reductase inhibitory activity of N-(quinolinyl thiocarbonyl) glycine derivatives

Doi:10.1016/0223-5234(92)90032-V
(1992)
Doi:10.1016/S0040-4039(00)72336-7
(1975)
A Highly Convergent Strategy Towards Rapamycin. Stereoselective Construction of the C⁸-C¹⁸ Fragment

Doi:10.1039/c39930000617
(1993)
[(4-Hydroxyl-benzo[4,5]thieno[3,2-c]pyridine-3-carbonyl)-amino]-acetic acid derivatives; HIF prolyl 4-hydroxylase inhibitors as oral erythropoietin secretagogues

Doi:10.1016/j.bmcl.2013.08.067
(2013)
Standardized intermediates for oligosaccharide synthesis. A convenient preparation of partially protected derivatives of allyl O-β-D-galactopyranosyl-(1->4)-β-D-glucopyranoside suitable for chain extension at position O-4'

Doi:10.1016/0008-6215(93)84191-8
(1993)
Synthesis and Structure-Activity Relationships of a Series of Penicillin-Derived HIV Proteinase Inhibitors: Heterocyclic Ring Systems Containing P'₁ and P'₂ Substituents

Doi:10.1021/jm00048a007
(1994)

Article Doi