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Glycoscience pp 305–342Cite as

C–C Bond Formation

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Abstract

In this chapter, synthetic methodologies for the preparation of C‐branched carbohydrates, and nucleosides will be summarized and discussed.

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Abbreviations

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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Acknowledgement

Financial support from NNSFC (Project 20621703) is gratefully acknowledged.

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Correspondence to Yuguo Du .

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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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