Hydrogen Transfer from 1-Naphthol Triplet to Ground-State Benzophenone: Kinetic Evidence against Proposed Exciplex Intermediacy

DOI: 10.1021/ja00239a067

Source and publish data:

Journal of the American Chemical Society p. 1600 - 1601 (1987)

Update date:2022-08-30

Topics:

Authors:

Gorman, A. A.

Hamblett, I.

Lambert, C.

Potter, R. C.

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

Article abstract of DOI:10.1021/ja00239a067

Full text of DOI:10.1021/ja00239a067

Products guided by the article

Product name:1-Naphthalenyloxy

Cas No:33490-96-9

R&D Labs maybe for 33490-96-9

Synasia Inc

Contact:17316303296

Address:240 Amboy Ave
Zhejiang Kaili Industrial Co., Ltd

Contact:+86-571-85241926

Address:lantian business center,No.18 Moganshan Road
NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China
Taizhou volsen chemical Co., Ltd

website:http://www.volsenchem.com

Contact:+86-576-88869393

Address:Jiaojiang District, Taizhou, Zhejiang, China.
Zhengzhou HQ Material Co.,Ltd

Contact:+86-371-67759225

Address:No.32, Jinsuo Road, High-tech Zone

Relevant to this article

A mild and efficient one-step synthesis of quinolines

Doi:10.1016/j.tetlet.2005.01.075
(2005)
Short, highly efficient syntheses of protected 3-azido- and 4-azidoproline and their precursors

Doi:10.1021/ol0161054
(2001)
DBU-catalyzed [3 + 2] cycloaddition and Michael addition reactions of 3-benzylidene succinimides with 3-ylidene oxindoles and chalcones

Doi:10.1039/c9ob00385a
(2019)
A New Directed Synthesis of Enol Borates from gem-Borazirconocene Alkanes, and their Regioselective Conversion to α-Bromo Ketones

Doi:10.1016/00404-0399(50)11182-
(1995)
Methoxylation of Singly Bonded 1,4-1′,4′-BnC₆₀-C₆₀Bn Dimer: Preferential Formation of 1,4-C₆₀ Adduct with Sterically Less Demanding Addends and Stability Difference between 1,2- and 1,4-OMe(Bn)C₆₀

Doi:10.1021/acs.joc.6b01171
(2016)
Identification and Synthesis of Impurities During a Novel Process Development of Rivaroxaban

Doi:10.1002/jhet.3355
(2018)

Article Doi