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

Gulang Hailun Fine Chemicals Co., Ltd.

Contact:13605738876 0573-84772866

Address:No. 4 Bridge, Xinjing port, Yaozhuang Town, Jiashan County, Zhejiang, China
SJZ Chenghui Chemical Co., Ltd.

Contact:86-311-87713916

Address:no.368 youyi north avenue
Nantong Kaixin Pharma Chemical Co.,Ltd.

Contact:86-513-85250786

Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China
Beijing Ribio Biotech Co.,Ltd

Contact:86-10-62664360

Address:Building 10,No.18 AnNingZhuang East Road, GuangHua Pioneer Park,HaiDian District, BeiJing China
Evershine Chemical CO Ltd

Contact:+86-571-87010026

Address:202, Zhenhua Road,

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