Abstract
In this chapter, synthetic methodologies for the preparation of C‐branched carbohydrates, and nucleosides will be summarized and discussed.
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- AIBN:
-
azobisisobutyronitrile
- CAN:
-
ceric(IV) ammonium nitrate
- CAMC:
-
3′‑β‑carbamoylmethylcytidine
- COT:
-
cyclooctatetraene
- DLP:
-
dilauoryl peroxide
- DMF:
-
dimethylformamide
- HDA:
-
hetero-Diels–Alder
- HMDS:
-
1,1,1,3,3,3-hexamethyldisilazane
- MBH:
-
Morita–Baylis–Hillman
- MDA:
-
methyl diazoacetate
- MMTr:
-
monomethoxytrityl
- TBS:
-
tert-butyldimethylsilyl
- TBAF:
-
tetra-n-butylammonium fluoride
- TBAI:
-
tetra-n-butylammonium iodide
- TBDPS:
-
tertbutyldiphenylsilyl
- TEA:
-
triethylamine
- TEDMS:
-
2-(trimethylsilyl)ethynyl]dimethylsilyl
- THF:
-
tetrahydrofuran
- THP:
-
tetrahydropyran
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Financial support from NNSFC (Project 20621703) is gratefully acknowledged.
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Du, Y., Chen, Q., Liu, J. (2008). C–C Bond Formation. In: Fraser-Reid, B.O., Tatsuta, K., Thiem, J. (eds) Glycoscience. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-30429-6_7
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DOI: https://doi.org/10.1007/978-3-540-30429-6_7
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