Synthesis of 1,2-disubstituted naphthalenes and tetrahydronaphthalenes from dihydronaphthalenes obtained by conjugate addition of organolithium reagents to 2,6-bis(tert-butyl)-4-methoxyphenyl naphthalenecarboxylates

DOI: 10.1248/cpb.47.1318

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1318 - 1321 (1999)

Update date:2022-07-29

Topics:

Authors:

Shindo, Mitsuru

Koga, Kenji

Tomioka, Kiyoshi

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

Article abstract of DOI:10.1248/cpb.47.1318

A method of the conversion of 2,6-bis(tert-butyl)-4-methoxyphenyl dihydronaphthalenecarboxylates into substituted naphthalenes and tetrahydronaphthalenes was developed. Aromatization of substituted dihydronaphthalenecarboxylates with 2,3-dichloro-5,6-dicy

Full text of DOI:10.1248/cpb.47.1318

NII-Electronic Library Service

Products guided by the article

Product name:trans-2,6-bis(tert-butyl)-4-methoxyphenyl 2-butyl-1,2-dihydro-1-naphthalenecarboxylate

Cas No:129633-47-2

R&D Labs maybe for 129633-47-2

Puyang Willing Chemicals Co.,Ltd.

Contact:86-393-4840366

Address:Puyang Henan China
ANHUI CHEM-BRIGHT BIOENGINEERING CO.,LTD

Contact:86-561-4080321

Address:No.8 Lieshan Industrial Zone of Huaibei
Jiaxing Barton Chemicals

website:http://www.chinabarton.com

Contact:+86-573-82719618

Address:No. 162 Fumin Road, Honghe Town,
Shanghai Witshoot Internet Technology Co Ltd

Contact:+86-21-66390020

Address:Room 419, No.285 Luochuan Road (E)
Zibo Linzi Darong Fine Chemical Co., Ltd(expird)

Contact:86-532-67773200; 15689126900

Address:Qidu town,Linzi district,Zibo city,Shandong province,China

Relevant to this article

Directed regiochemical control in the ring expansion reactions of a substituted trans-decalone

Doi:10.1016/S0040-4039(00)88999-6
(1990)
Design and synthesis of thiolesters for the histochemical demonstration of esterase and lipase via the formation of osmiophilic diazo thioethers.

Doi:10.1021/jm00321a005
(1966)
Stereospecific Synthesis of Racemic cis- and trans-6-Trifluoromethylshikimic Acids

Doi:10.1039/P19900001281
(1990)
Doi:10.1002/hlca.19510340531
(1951)
Studying competitive lithiations at alpha-, ortho-, and benzylic positions in various N-protected aniline derivatives

Doi:10.1016/j.tet.2011.02.056
(2011)
Reactions of Thermally Generated tert-Butyl and Di(tert-alkyl)ketyl Radicals in Toluene: Cage Effects and Hydrogen Transfer

Doi:10.1021/jo00001a034
(1991)

Article Doi