Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes: a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor

Michael Wallace; Elizabeth Ficko-Blean; Keith Stubbs

doi:10.1021/acs.joc.0c02339

Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes: a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor

Michael Wallace, Elizabeth Ficko-Blean, Keith Stubbs

School of Molecular Sciences

Research output: Contribution to journal › Article › peer-review

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Original language	English
Pages (from-to)	16182-16195
Number of pages	14
Journal	The Journal of Organic Chemistry
Volume	85
Issue number	24
DOIs	https://doi.org/10.1021/acs.joc.0c02339
Publication status	Published - 18 Dec 2020

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10.1021/acs.joc.0c02339

Wallace at al., 2020 Red algal molecules Accepted author manuscript, 482 KB

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@article{c37c6bd8f4ae42268aafbd76c23be0fe,

title = "Red algal molecules - Synthesis of methyl neo-{\ss}-carrabioside and its S-linked variant via two synthetic routes: a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor",

author = "Michael Wallace and Elizabeth Ficko-Blean and Keith Stubbs",

year = "2020",

month = dec,

day = "18",

doi = "10.1021/acs.joc.0c02339",

language = "English",

volume = "85",

pages = "16182--16195",

journal = "The Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "24",

}

Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes : a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor. / Wallace, Michael; Ficko-Blean, Elizabeth; Stubbs, Keith.

In: The Journal of Organic Chemistry, Vol. 85, No. 24, 18.12.2020, p. 16182-16195.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes

T2 - a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor

AU - Wallace, Michael

AU - Ficko-Blean, Elizabeth

AU - Stubbs, Keith

PY - 2020/12/18

Y1 - 2020/12/18

UR - http://www.scopus.com/inward/record.url?scp=85096552363&partnerID=8YFLogxK

U2 - 10.1021/acs.joc.0c02339

DO - 10.1021/acs.joc.0c02339

M3 - Article

C2 - 33182999

VL - 85

SP - 16182

EP - 16195

JO - The Journal of Organic Chemistry

JF - The Journal of Organic Chemistry

SN - 0022-3263

IS - 24

ER -

Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes: a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor

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The Development of Tools to Study Carbohydrate-Processing Enzymes Implicated in Human Disease

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Red algal molecules - Synthesis of methyl neo-ß-carrabioside and its S-linked variant via two synthetic routes: a late stage ring closure and using a 3,6-anhydro-D-galactosyl donor

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The Development of Tools to Study Carbohydrate-Processing Enzymes Implicated in Human Disease

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