Scholarly article on 9-Azatricyclo[3.3.1.02,4]nonan-7-one,9-methyl-(9CI) 564474-92-6 from Journal of the American Chemical Society p. 215 - 216

DOI: 10.1021/ja01029a054

Source and publish data:

Journal of the American Chemical Society p. 215 - 216 (1969)

Update date:2022-08-03

Topics:

Authors:

Chapman,O.L.

Fugiel,R.A.

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

Article abstract of DOI:10.1021/ja01029a054

Full text of DOI:10.1021/ja01029a054

Products guided by the article

Product name:9-Azatricyclo[3.3.1.02,4]nonan-7-one,9-methyl-(9CI)

Cas No:564474-92-6

R&D Labs maybe for 564474-92-6

BAODING SINO-CHEM INDUSTRY CO.,LTD

Contact:0312-5956088

Address:NO.8 FUXING ROAD,CHINA
Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
HANGZHOU PANYU CHEMICAL CO.,LIMITED

Contact:+86-571-86578491

Address:Rm 605, NO.1870 Binsheng Road,Binjiang Dist, Hangzhou, China
Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China

Relevant to this article

Zn-mediated asymmetric allylation of N-tert-butanesulfinyl ketimines: An efficient and practical access to chiral quaternary 3-aminooxindoles

Doi:10.1039/c2cc38600c
(2013)
Novel in vivo active anti-malarials based on a hydroxy-ethyl-amine scaffold

Doi:10.1016/j.bmcl.2012.11.118
(2013)
Optically active α-phenylethylamine as efficient organocatalyst in the solvent-free reactions between 2,3-butanedione and conjugated nitroolefins

Doi:10.1002/chir.22088
(2012)
Structure-activity relationship study on benzoic acid part of diphenylamine-based retinoids

Doi:10.1016/j.bmcl.2012.11.008
(2013)
An enantioselective strategy for the synthesis of (S)-tylophorine via one-pot intramolecular schmidt/bischler-napieralski/imine-reduction cascade sequence

Doi:10.1021/jo302725q
(2013)
Copper-catalyzed ring opening of furans as a concise route to polysubstituted furans under mild conditions

Doi:10.1055/s-0032-1317683
(2012)

Article Doi

DOI: 10.1021/ja01029a054