## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Efficient Synthesis of Resin-Bound α-TMSdiazoketones and Their Use in Solid-Phase Organic Synthesis
✍ Scribed by Yasuyoshi Iso; Hirohisa Shindo; Hiroshi Hamana
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 183 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
AbstractÐa-TMSdiazoketones on a solid support could be simply and ef®ciently prepared by reaction of the corresponding resin-bound acid chlorides with excess TMSdiazomethane, without any bases. These a-TMSdiazoketones were used via carbenes or carbenoids for a variety of solid-phase reactions. These useful solid-phase reactions allow ef®cient construction of diverse compound libraries by use of combinatorial chemistry, due to the high reactivity and wide applications of the carbenes or carbenoids.
📜 SIMILAR VOLUMES
Mild and efficient preparation of acid-labile resins with displaceable halide linkers (3 and 4, X = Br and 1) is described. These resins can be used in combinatorial organic synthesis of numerous drug-scaffold libraries, Their synthetic utility is exemplified by high yielding N-alkylations with stru
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract Well‐characterized resins of high purity are critical for effective solid phase peptide synthesis (SPPS). The quality of commercial (4‐methyl)benzhydrylamine‐resin (MBHA‐resin), used for the synthesis of peptide amides, is not consistent and residual ketone functionalities are frequentl