Reaction of lithiated senecioamide and related compounds with benzynes: Efficient syntheses of naphthols and naphthoquinones

DOI: 10.1248/cpb.34.2810

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2810 - 2820 (1986)

Update date:2022-08-04

Topics:

Authors:

Watanabe

Hisamatsu

Hotokezaka

Furukawa

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

Article abstract of DOI:10.1248/cpb.34.2810

Full text of DOI:10.1248/cpb.34.2810

NII-Electronic Library Service

Products guided by the article

Product name:N,N-diethyl-2-isopropenyl-2-(3'-methoxyphenyl)acetamide

Cas No:106914-38-9

R&D Labs maybe for 106914-38-9

Tianjin Anda North Industrial & Business Co.Ltd.

Contact:86-22-24999306

Address:No.11 Erwei Road,Dongli Development Area,Tianjin,China
Changsha Yonta Industry Co., Ltd.

Contact:+ 86-731-8535 2228

Address:Rm.1717, North Bldg., No.368, East 2nd Ring Road(2nd Section)
Jiangyin Tenghua Import&Export Co.,Ltd.

Contact:+86-510-86263875

Address:Room 402-B,9 Yanling Road, Jiangyin,Jiangsu, China
Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
Wuhan Silworld Chemical Co.,Ltd

website:http://www.silworldchemical.com

Contact:+86-27-85613400

Address:No.198 jiangjun Road, Wuhan,China 430033

Relevant to this article

OXIDATIVE ADDITION REACTIONS OF Cp*OS(CO)PMe2Ph)Me (Cp*= η⁵ -C5Me5). ISOLATION OF INTERMEDIATES DURING ALKYL-METAL ELECTROPHILIC CLEAVAGE REACTIONS

Doi:10.1016/0022-328X(86)80185-1
(1986)
Multistep oxidase-lyase reactions: Synthesis of optically active 2-hydroxyketones by using biobased aliphatic alcohols

Doi:10.1002/cctc.201300093
(2013)
Doi:10.1021/ja01138a519
(1952)
Doi:10.1007/BF00477468
()
Coordination modes of cis-P,P′-diphenyl-1,4-diphospha-cyclohexane to metal ions of Groups 9 and 10

Doi:10.1016/S0020-1693(02)01211-2
(2003)
Highly efficient palladium-catalyzed cross-coupling of diarylborinic acids with arenediazoniums for practical diaryl synthesis

Doi:10.1016/j.tetlet.2019.151491
(2020)

Article Doi