Scholarly article on 1-acetyl-3-butyl-4-phenyl-piperidin-4-ol 101866-62-0 from Journal of the American Chemical Society p. 3966,3969

DOI: 10.1021/ja01500a043

Source and publish data:

Journal of the American Chemical Society p. 3966,3969 (1960)

Update date:2022-08-03

Topics:

Authors:

McElvain

Remy Remy

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

Article abstract of DOI:10.1021/ja01500a043

Full text of DOI:10.1021/ja01500a043

Products guided by the article

Product name:1-acetyl-3-butyl-4-phenyl-piperidin-4-ol

Cas No:101866-62-0

R&D Labs maybe for 101866-62-0

Hangzhou LINGEBA Technology Co., Ltd.

Contact:+0086-571-87389059

Address:Office 1-913,NewYouth Plaza, GongShu Area, HangZhou,ZheJiang,P.R.China
SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
Shandong General Materials Co.,Ltd（Shandong Aoertong Chemical Co., Ltd）

Contact:86-531-88072280

Address:No. 1825 Hualong Road, Licheng District, Jinan, Shandong, China
Suzhou Kangrun Pharmaceutical, Inc

Contact:86-512-63912376，63913329

Address:Building 2, No. 2358 ,Chang'an Rd, Wujiang Economic Development Zone Pioneering park, china
Chengdu Push Bio-technology Co., Ltd

Contact:--

Address:No.8 Wuke West Second Road, Wuhou

Relevant to this article

Doi:10.1021/jo01280a064
(1967)
Preparation of ω-hydroxy acids by reduction of α,ω-methylene diesters with NaBH₄

Doi:10.1080/00397919708004080
(1997)
Doi:10.1039/jr9620004286
(1962)
Regioselective Synthesis of α-Functional Stilbenes via Precise Control of Rapid cis- trans Isomerization in Flow

Doi:10.1021/acs.orglett.1c00538
(2021)
Sc-catalyzed aldol-yype additions of N-Benzoylcyclopropanecarboxamides via iodide-mediated ring-opening: Stereoselective synthes of □-Lactams

Doi:10.1021/ol800401g
(2008)
One-Pot Substitution of Aliphatic Alcohols Mediated by Sulfuryl Fluoride

Doi:10.1002/chem.202000721
(2020)

Article Doi

DOI: 10.1021/ja01500a043