- Title
- Dual-Catalyst Acceleration of Tandem Disulfide Cleavage and Baylis–Hillman Synthesis of 2 H-1-Benzothiopyran Derivatives
- Creator
- Nyoni, Dubekile, Lobb, Kevin A, Kaye, Perry T
- Subject
- To be catalogued
- Date
- 2013
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/448898
- Identifier
- vital:74769
- Identifier
- xlink:href="https://doi.org/10.1080/00397911.2012.673449"
- Description
- While both 1,8-diazabicyclo[5.4.0]undec-7-ene and triphenylphosphine catalyze tandem Baylis–Hillman reaction/disulfide cleavage of 2,2′-dithiodibenzaldehyde independently, when used together as a dual-catalyst system, the overall yields of the cyclized 2H-1-benzothiopyrans are consistently greater and the reaction time decreases dramatically.
- Format
- computer, online resource, application/pdf, 1 online resource (5 pages), pdf
- Publisher
- Taylor and Francis
- Language
- English
- Relation
- Synthetic Communications, Nyoni, D., Lobb, K.A. and Kaye, P.T., 2013. Dual-Catalyst Acceleration of Tandem Disulfide Cleavage and Baylis–Hillman Synthesis of 2 H-1-Benzothiopyran Derivatives. Synthetic Communications, 43(13), pp.1837-1841, Synthetic Communications volume 43 number 13 p. 1837 2013 1532-2432
- Rights
- Publisher
- Rights
- Use of this resource is governed by the terms and conditions of the Taylor and Francis Online Terms and Conditions Statement (https://www.tandfonline.com/terms-and-conditions)
- Rights
- Closed Access
- Hits: 7
- Visitors: 5
- Downloads: 0
Thumbnail | File | Description | Size | Format | |||
---|---|---|---|---|---|---|---|
View Details | SOURCE1 | Dual-Catalyst Acceleration of Tandem Disulfide Cleavage and Baylis–Hillman Synthesis of 2 H-1-Benzothiopyran Derivatives.pdf | 650 KB | Adobe Acrobat PDF | View Details |