Scholarly article on 2-Hydroxy-chinolizidin 148407-30-1 from Journal of the American Chemical Society p. 1832,1835

DOI: 10.1021/ja01636a029

Source and publish data:

Journal of the American Chemical Society p. 1832,1835 (1954)

Update date:2022-08-03

Topics:

Authors:

Boekelheide

Gall Gall

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

Article abstract of DOI:10.1021/ja01636a029

Full text of DOI:10.1021/ja01636a029

Products guided by the article

Product name:2-Hydroxy-chinolizidin

Cas No:148407-30-1

R&D Labs maybe for 148407-30-1

Xian Changyue Biological Technology Co., Ltd.

website:https://www.xachangyue.com/

Contact:+86-029-88211911

Address:Keji Road NO.70
SHENZHEN PENGCHENG REDSTAR INDUSTRY CO.,LTD

Contact:+86-755-82412922

Address:Room 8066, East Block, Square City, Jiabin Road, Luohu District
taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
Golden Union Agrochemical Import and Export Co., Ltd.

Contact:86-755-23910527

Address:Room 1106, Tower 3A, Excellence Century Center, Futian District, Shenzhen, China
YORK CHEMICALS LTD

Contact:+1 (647) 918 5848

Address:2343 BRIMLEY RD., Suite 250

Relevant to this article

Synthesis of 4-silapiperidine building blocks with N-H groups using the Staudinger reaction

Doi:10.1021/om400873w
(2013)
Calix[6]arene sulfonic acids catalysed Michael reactions of indoles with α,β-unsaturated ketones in water assisted by microwave radiation

Doi:10.3184/174751913X13734725288804
(2013)
Substitution of fluorine in C6F5X (X = COOMe, CF3, CN, NO2) and pentafluoropyridine by the triethylgermyl group

Doi:10.1016/0022-328X(93)80066-K
(1993)
Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol

Doi:10.1002/anie.201802533
(2018)
Synthesis of a disulfide functionalized diacetylenic derivative of carbazole as building-block of polymerizable self-assembled monolayers

Doi:10.2478/s11696-013-0437-2
(2014)
Doi:10.1021/ja01127a026
(1952)

Article Doi

DOI: 10.1021/ja01636a029