Tricyclo1,6>decane-Tricyclo1,5>decane Interconversions. Propellane Rearrangements and a Nonphotochemical Propellane Synthesis

DOI: 10.1021/ja00541a077

Source and publish data:

Journal of the American Chemical Society p. 6636 - 6638 (1980)

Update date:2022-08-04

Topics:

Authors:

Eaton, Philip E.

Jobe, Patrick G.

Nyi, Kayson

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

Article abstract of DOI:10.1021/ja00541a077

Full text of DOI:10.1021/ja00541a077

Products guided by the article

Product name:1H-1,3a-Ethanopentalen-1-ol, hexahydro-

Cas No:75594-32-0

R&D Labs maybe for 75594-32-0

Hubei Xiangxi Chemical Industry Co.,Ltd

Contact:+86-710-3454830

Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China
JIEJIE GROUP CO.,LTD.

Contact:+86 021-51698675

Address:1701, Jielong Plaza, No.618 Pingliang Rd, ShangHai,China
Changzhou Screw International Trading Co., Ltd.

Contact:13906149256,18001495888

Address:Jiangsu，Jintanqu
Zhejiang Hoshine Silicon Industry Co., Ltd.

Contact:86-573-89179966

Address:Zhapu Town, Pinghu City, Zhejiang, China
Chengdu Biopurify Phytochemicals Ltd.

website:http://www.phytopurify.com

Contact:+86-28-82633397

Address:2F,No.11 Building,No.388 Rongtaidadao CNSTP,Wenjiang Zone,Chengdu,Sichuan, China

Relevant to this article

Doi:10.1021/ja01330a074
(1933)
Secondary Amines from the Iron(II) Ion-Catalyzed Reaction of Amine Oxides: A General Method for the Dealkylation of Tertiary Amines

Doi:10.1055/s-1985-31342
(1985)
Comparison of the Suzuki cross-coupling reactions of 4,7-dichloroquinoline and 7-chloro-4-iodoquinoline with arylboronic acids using phosphine-free palladium catalysis in water

Doi:10.1139/v03-187
(2004)
Doi:10.1007/BF00471197
()
Synthesis, crystal structure, vibrational spectra, and thermochemical transformations of tris(hydroxymethyl)aminomethane

Doi:10.1134/S0036023614010069
(2014)
Biotransformation of 20(S)-protopanaxatriol by Aspergillus niger and the cytotoxicity of the resulting metabolites

Doi:10.1016/j.phytol.2014.11.006
(2015)

Article Doi