REGIOSELECTIVE REDUCTIVE ELIMINATION OF ARYLOXYMETHYLETHYNYLCARBINOLS - SYNTHESIS OF ARYLOXYMETHYLALLENES

DOI: 10.1016/S0040-4039(00)83878-2

Source and publish data:

Tetrahedron Letters p. 3777 - 3780 (1986)

Update date:2022-08-04

Topics:

Authors:

Rajamannar, T.

Balasubramanian, K. K.

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

Article abstract of DOI:10.1016/S0040-4039(00)83878-2

Exclusive formation of allenes and alkenols during the reduction of aryloxymethylethynylcarbinols and ethynylcarbinols respectively, with lithium aluminiumhydride, is being reported.

Full text of DOI:10.1016/S0040-4039(00)83878-2

Products guided by the article

Product name:2-(exo-1-phenoxypropynyl)bicyclo<2.2.1>hept-5-ene-endo-2-ol

Cas No:108574-74-9

R&D Labs maybe for 108574-74-9

Zhuhai Rundu Pharmaceutical co.,Ltd

Contact:+86-756-7630755

Address:No.6,North Airport Road,Sanzao Town,Jinwan District
Zibo Jujin Chemical Industry Co., Ltd.（Dongming Jujin Chemical Industry Co., Ltd. ）

Contact:+86-533-2975022

Address:No.99 Shanquan Road, Zhangdian District
Wuhan Better Organic Technology Inc.

Contact:13307163183

Address:Wuhan Economic&Technology Development Zone, Hubei
GLD peptide scientific lnc.

Contact:21-7631221 15884421033

Address:326 Science and technology,Shanghai,China
shandong zhongke taidou chemical co.,ltd

Contact:86-531-88682301

Address:Jinan shandong Province CHina

Relevant to this article

Bronsted acid catalyzed propargylation of 1,3-dicarbonyl derivatives. Synthesis of tetrasubstituted furans

Doi:10.1021/ol0631298
(2007)
Synthesis and reactivity of homo- and hetero-dimetallic complexes bridged by diphenyl-2-pyridylphosphine and hydrides: Regioselectivity of alkyne insertion into unsaturated M¹(μ-PPh₂Py)(μ-H) ₂M² moieties

Doi:10.1039/b815890h
(2009)
Enantioselective synthesis of oasomycin A, part II: Synthesis of the C29-C46 subunit

Doi:10.1002/anie.200603654
(2007)
Doi:10.1021/ja00906a041
(1963)
Dibutyltin oxide catalyzed selective sulfonylation of α-chelatable primary alcohols

Doi:10.1021/ol990658l
(1999)
A concise synthesis of Tamiflu: third generation route via the Diels-Alder reaction and the Curtius rearrangement

Doi:10.1016/j.tetlet.2006.12.093
(2007)

Article Doi