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 | |
| State | Published - Dec 1 1995 |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
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A synthesis of the 4-alkylamino-2, 4-dideoxy-l-thero-pentopyranose components of the calicheamicins and esperamicins. / Mash, Eugene A; Nimkar, Sandeep K.; DeMoss, Suzanne M.
In: Journal of Carbohydrate Chemistry, Vol. 14, No. 9, 01.12.1995, p. 1369-1378.Research output: Contribution to journal › Article
}
TY - JOUR
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.
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.
UR - http://www.scopus.com/inward/record.url?scp=45149133385&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=45149133385&partnerID=8YFLogxK
U2 - 10.1080/07328309508005417
DO - 10.1080/07328309508005417
M3 - Article
AN - SCOPUS:45149133385
VL - 14
SP - 1369
EP - 1378
JO - Journal of Carbohydrate Chemistry
JF - Journal of Carbohydrate Chemistry
SN - 0732-8303
IS - 9
ER -