A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins

Eugene A. Mash; Sandeep K. Nimkar; Suzanne M. DeMoss

doi:10.1080/07328309508005417

A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins

Eugene A. Mash
, Sandeep K. Nimkar
, Suzanne M. DeMoss

Chemistry and Biochemistry

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

3 Scopus citations

Abstract

A general synthetic approach to enantiomerically pure 4-substituted has been developed which provides access to the 4-alkylamino-2, 4-dideoxy-L-r/zreo-pentopyranose components of the calicheamicins and esperamicins.

Original language	English (US)
Pages (from-to)	1369-1378
Number of pages	10
Journal	Journal of Carbohydrate Chemistry
Volume	14
Issue number	9
DOIs	https://doi.org/10.1080/07328309508005417
State	Published - Dec 1 1995

ASJC Scopus subject areas

Biochemistry
Organic Chemistry

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10.1080/07328309508005417

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title = "A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins",

abstract = "A general synthetic approach to enantiomerically pure 4-substituted has been developed which provides access to the 4-alkylamino-2, 4-dideoxy-L-r/zreo-pentopyranose components of the calicheamicins and esperamicins.",

author = "Mash, \{Eugene A.\} and Nimkar, \{Sandeep K.\} and DeMoss, \{Suzanne M.\}",

note = "Funding Information: Support of this research by the Elsa U. Pardee Foundation is gratefully acknowledged.",

year = "1995",

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language = "English (US)",

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journal = "Journal of Carbohydrate Chemistry",

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T1 - A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins

AU - Mash, Eugene A.

AU - Nimkar, Sandeep K.

AU - DeMoss, Suzanne M.

N1 - Funding Information: Support of this research by the Elsa U. Pardee Foundation is gratefully acknowledged.

PY - 1995/12/1

Y1 - 1995/12/1

N2 - A general synthetic approach to enantiomerically pure 4-substituted has been developed which provides access to the 4-alkylamino-2, 4-dideoxy-L-r/zreo-pentopyranose components of the calicheamicins and esperamicins.

AB - A general synthetic approach to enantiomerically pure 4-substituted has been developed which provides access to the 4-alkylamino-2, 4-dideoxy-L-r/zreo-pentopyranose components of the calicheamicins and esperamicins.

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DO - 10.1080/07328309508005417

M3 - Article

AN - SCOPUS:45149133385

SN - 0732-8303

VL - 14

SP - 1369

EP - 1378

JO - Journal of Carbohydrate Chemistry

JF - Journal of Carbohydrate Chemistry

IS - 9

ER -

A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins

Abstract

ASJC Scopus subject areas

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