?-Facial Stereoselectivity: Rates and Stereoselectivities of Cycloadditions of Hexachlorocyclopentadiene to 7-Substituted Norbornadienes, and Photoelectron Spectral and Molecular Orbital Computational Investigations of Norbornadienes

DOI: 10.1021/ja00541a017

Source and publish data:

Journal of the American Chemical Society p. 6482 - 6490 (1980)

Update date:2022-08-05

Topics:

Authors:

Mazzocchi, Paul H.

Stahly, Barbara

Dodd, John

Rondan, Nelson G.

Domelsmith, L.N.

et al. et al.

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

Article abstract of DOI:10.1021/ja00541a017

The partial rate factors for the Diels-Alder cycloadditions of hexachlorocyclopentadiene to 7-substituted norbornadienes in the four possible modes were measured.Syn-endo and anti-endo rates are essentially identical and decrease slightly as the effective

Full text of DOI:10.1021/ja00541a017

Products guided by the article

Product name:C₁₉H₁₄Cl₆

Cas No:74985-34-5

R&D Labs maybe for 74985-34-5

Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Huangshi Meifeng Chemical Co.,ltd.

Contact:+86-714-6516706

Address:1941-4-3#,Hubin Avenue,Huangshi,Hubei,China
Shangyu Sanhechemicals Co.,LTD.

Contact:86-0571-56696839

Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China
Zhejiang Rongkai Chemical Technology Co.,Ltd.

Contact:+86-578-8185786

Address:Shangjiang Industrial Zone,Suichang
Beijing Century Richap Chemistry Co.,Ltd

Contact:+86- 010-64455497

Address:Guannan County, Lianyungang City, Jiangsu Province, China

Relevant to this article

Synthesis of tritium labelled 3(R)-HETE and 3(R),18(R/S)-DiHETE through a common synthetic route

Doi:10.1002/jlcr.791
(2004)
SUBSTITUTION NUCLEOPHILE AROMATIQUE RADICALAIRE (1) SYNTHESE DIRECTE DE 4-AZA-INDOLES DANS DES CONDITIONS NON ACIDES ET DOUCES

Doi:10.1016/S0040-4039(00)93652-9
(1980)
Proton Nuclear Magnetic Resonance Study of the Addition of Methoxide Ion to 2,4,6-Triphenylpyrylium, 2,4,6-Triphenylthiopyrylium, 1,2,4,6-Tetraphenylpyridinium, and 1-(p-Nitrophenyl)-2,4,6-triphenylpyridinium Cations

Doi:10.1021/jo01313a027
(1980)
Preparation and electrophilic substitution of 1-trimethylsilylpentadienyllithium

Doi:10.1002/hlca.19800630302
(1980)
Syntheses and evaluation of ketals, hemithioketals, and dithioketals of conjugated styryl ketones principally for antineoplastic activity

Doi:10.1002/jps.2600690527
(1980)
Synthesis of potential antineoplastic agents. 35. Phosphorus-containing structural analogs of myleran.

Doi:10.1021/jm00320a018
(1966)

Article Doi