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

Hangzhou Haiqiang Chemical Co.,Ltd.

Contact:+86-571-86960370

Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China
Pale Palm Imex

Contact:+36(21)2523420

Address:Head office: 1102 Budapest, SZENT LASZLO TER 24/B. 1/1., HUNGARY / CHINA
Nanjing Qirui Material Co., Ltd.

Contact:+86-25-52320053

Address:F4-5, #17 Building, Chuang Yi Yuan, No.6 Guanghua East Street, Nanjing, 210007 P.R.China
Xiamen Hisunny Chemical Co.,Ltd

website:http://www.hisunnychem.com

Contact:+86-592-3327115

Address:Unit 603,No.879,Xiahe Road,Meixin Building,Xiamen,China
KINHENG CHEMICAL(SHANGHAI)CO., LTD.

Contact:+8621-60490170

Address:Room401, No.28,Lane 189, Yangshupu Rd. Shanghai, China.

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