Synthesis of the Mannosidase II Inhibitor Mannostatin A

Spencer Knapp; T. G.Murali Dhar

doi:10.1021/jo00013a006

Synthesis of the Mannosidase II Inhibitor Mannostatin A

Spencer Knapp, T. G.Murali Dhar

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

46 Scopus citations

Abstract

The synthesis of mannostatin A (1), a new inhibitor of glycoprotein processing, has been accomplished in stereocontrolled fashion starting from D-ribonolactone, 7 (~32% overall yield).

Original language	English (US)
Pages (from-to)	4096-4097
Number of pages	2
Journal	Journal of Organic Chemistry
Volume	56
Issue number	13
DOIs	https://doi.org/10.1021/jo00013a006
State	Published - Jun 1 1991

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1021/jo00013a006

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title = "Synthesis of the Mannosidase II Inhibitor Mannostatin A",

abstract = "The synthesis of mannostatin A (1), a new inhibitor of glycoprotein processing, has been accomplished in stereocontrolled fashion starting from D-ribonolactone, 7 (~32% overall yield).",

author = "Spencer Knapp and Dhar, {T. G.Murali}",

year = "1991",

month = jun,

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doi = "10.1021/jo00013a006",

language = "English (US)",

volume = "56",

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journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

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AU - Knapp, Spencer

AU - Dhar, T. G.Murali

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N2 - The synthesis of mannostatin A (1), a new inhibitor of glycoprotein processing, has been accomplished in stereocontrolled fashion starting from D-ribonolactone, 7 (~32% overall yield).

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JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 13

ER -

Synthesis of the Mannosidase II Inhibitor Mannostatin A

Abstract

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