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

AURORA CHEMICAL CO., LTD

Contact:86-532-68629711 13780605697

Address:NO 220 YANAN 3 ROAD,(POST ADMINISTRATION BUILDING),QINGDAO,CHINA
Wuxi Pharma-Trading Import & Export Co.,Ltd.

Contact:+86-510-82304590 82716390

Address:Room 523,Youzu Alliance Building,No.88 Renmin Zhonglu,Wuxi,Jiangsu,China
SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai
Nanjing lanbai chemical Co.,Ltd.

Contact:+86-25-85499326

Address:Room 908, 9F Taiyue Building,No.285 Heyan Road
Hebei Maison Chemical Co.,Ltd

website:http://www.maisonchem.com.cn

Contact:0086-311-83833777

Address:Leitou industrial district, xinji, shijiazhuang city, hebei province,

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