?-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

Quzhou Aokai Chemical Co., Ltd.

Contact:86-570-3032832

Address:NO.16 , Laodong Road,Quzhou City, Zhejiang Province,China
Jinan Trio PharmaTech Co., Ltd

Contact:86-531-88811783；+(0)13153010282

Address:2766 Yingxiu Road, Jinan High-Tech Zone, China
Hangzhou Zhenghan Biological Technology Co., Ltd.

Contact:86-571-88781753

Address:liangzhu yuhang hangzhou city
Shanghai Coupling Pharmaceutical R&D Co., Ltd.(expird)

Contact:+86 021 50106671

Address:403 Room No.4 Buiding, No. 526 Ruiqing Road, Shanghai Zhangjiang Hi-Tech Park
WENZHOU M&C FOREIGN TRADE CO.,LTD.

Contact:+86-577-88862917

Address:No.8 Liming West Road,Wenzhou,zhejiang,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