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

ClickChem Technology Co., Limited

Contact:+86-0310-6519966/0531-52893837

Address:No.750 Shunhua Road, High-Tech Zone, Jinan city, Shandong China
Oren Hydrocarbons (Qingdao) Co., Ltd.

Contact:+86-532-68607667-801

Address:Room 3 # 302, No.9 Qingyun Road, Qingdao, China
Second Pharma Co., Ltd

Contact:+86-575-82733999 0575-82732999

Address:hangzhou gulf fine chemical zone,shangyu city,zhejiang province
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing

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