https://scholars.lib.ntu.edu.tw/handle/123456789/575812
Title: | 1,3-Dithiolanes (Update 2018) | Authors: | MAN-KIT LEUNG Chou C.-M Luh T.-Y. |
Issue Date: | 2018 | Journal Volume: | 2 | Start page/Pages: | 389-463 | Source: | Science of Synthesis | Abstract: | For previously published information, see Section 30.3.3.1. Although 1,3-dithiolanes are stable under both basic and acidic conditions, and can resist attack from certain nucleophiles, organometallic reagents, hydrides, and mild oxidizing agents, they can be effectively converted back into carbonyl groups under various mild conditions. Therefore, the use of a 1,3-dithiolane as a protective group for carbonyl functionalities has been extensive. During the last decades, many different kinds of effective catalysts have been developed to convert carbonyl compounds into 1,3-dithiolanes. ? 2018 Georg Thieme Verlag. All rights reserved. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85066897805&doi=10.1055%2fsos-SD-130-00179&partnerID=40&md5=919b3769b9943808349f3726478b9d6d https://scholars.lib.ntu.edu.tw/handle/123456789/575812 |
ISSN: | 25105469 | DOI: | 10.1055/sos-SD-130-00179 |
Appears in Collections: | 化學系 |
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