Synthesis of the liposidomycin diazepanone nucleoside

Spencer Knapp; Gregori J. Morriello; George A. Doss

doi:10.1021/ol0102904

Synthesis of the liposidomycin diazepanone nucleoside

Spencer Knapp, Gregori J. Morriello, George A. Doss

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

39 Scopus citations

Abstract

(formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochemistry of the liposidomycins 1 and 2 as 5′S,6′S,2‴S,3‴S.

Original language	English (US)
Pages (from-to)	603-606
Number of pages	4
Journal	Organic letters
Volume	4
Issue number	4
DOIs	https://doi.org/10.1021/ol0102904
State	Published - Feb 21 2002

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol0102904

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title = "Synthesis of the liposidomycin diazepanone nucleoside",

abstract = "(formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochemistry of the liposidomycins 1 and 2 as 5′S,6′S,2‴S,3‴S.",

author = "Spencer Knapp and Morriello, {Gregori J.} and Doss, {George A.}",

year = "2002",

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doi = "10.1021/ol0102904",

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AU - Doss, George A.

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N2 - (formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochemistry of the liposidomycins 1 and 2 as 5′S,6′S,2‴S,3‴S.

AB - (formula presented) The synthesis of the liposidomycin degradation product 4 from D-glucose establishes its stereochemistry as 5′S,6′S and, by incorporation of the earlier diazepanone relative stereochemical assignment, establishes the absolute stereochemistry of the liposidomycins 1 and 2 as 5′S,6′S,2‴S,3‴S.

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Synthesis of the liposidomycin diazepanone nucleoside

Abstract

All Science Journal Classification (ASJC) codes

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