![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Recent work from this laboratory has demonstrated that readily prepared lithium naphthalenide (2) at -70° is capable of the rapid reductive lithiation of cyclopropanone dithioketals (1) to sulfur-stabilized cyclopropyllithiums (4),1 ketene phenylthio-acetals (8) to sulfur-stabilized vinyllithiums (9) which are acyl anion equivalents,2 and a 1,1,3-tris(phenylthio)alkene (11) to the lithio derivative (12) of an α,β-unsaturated thioacetal.3,4
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.