| Tag |
First Indicator |
Second Indicator |
Subfields |
| LEADER |
00000ctm a22000005a 4500 |
| 001 |
in00001315513 |
| 005 |
20220103114156.0 |
| 007 |
cr unu a |
| 008 |
960813s1995 xx a b 000 0 eng d |
| 035 |
|
|
|9 AHB7886AM
|
| 035 |
|
|
|a (OCoLC)35231020
|
| 040 |
|
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|a TXA
|c TXA
|d UtOrBLW
|
| 049 |
|
|
|a TXAM
|a TXAR
|
| 099 |
|
|
|a 1995
|a Thesis
|a F348
|
| 100 |
1 |
|
|a Falahatpisheh, Nikoo.
|
| 245 |
1 |
0 |
|a Glycosyl tetrazoles as glycosyl donors for the synthesis of 2-deoxy glycosides /
|c by Nikoo Falahatpisheh.
|
| 246 |
3 |
|
|a Glycosyl tetrazoles as glycosyl donors for the synthesis of two-deoxy glycosides
|
| 264 |
|
1 |
|a [Place of publication not identified] :
|b [publisher not identified] ;
|c 1995.
|
| 300 |
|
|
|a xiii, 107 leaves :
|b illustrations ;
|c 28 cm.
|
| 336 |
|
|
|a text
|b txt
|2 rdacontent
|
| 337 |
|
|
|a computer
|b c
|2 rdamedia
|
| 338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
| 500 |
|
|
|a "Major subject: Chemistry".
|
| 500 |
|
|
|a In title, numerals are used.
|
| 500 |
|
|
|a Vita.
|
| 502 |
|
|
|b M.S.
|c Texas A&M University
|d 1995.
|
| 504 |
|
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|a Includes bibliographical references.
|
| 520 |
|
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|a 2-Deoxy oligosaccharides form a major component of
|
| 520 |
|
|
|a antibiotics. The instability of 2-deoxy oligosaccharides and
|
| 520 |
|
|
|a assembly of a trisaccharide model system of PI-080.
|
| 520 |
|
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|a biologically active aureolic acid and angucycline
|
| 520 |
|
|
|a butylphosphoramidite produces N2 and N1 isomer of the
|
| 520 |
|
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|a Condensation of 2-deoxy sugars with 1H-tetrazole and di-t-
|
| 520 |
|
|
|a conditions. Repetition of the coupling protocol enables the
|
| 520 |
|
|
|a difficulty in controlling their stereoselectivity of coupling
|
| 520 |
|
|
|a glycosyl donors were examined under different glycosylation
|
| 520 |
|
|
|a in the synthesis of oligosaccharides.
|
| 520 |
|
|
|a reactions is primarily due to the lack of a C-2 substituent.
|
| 520 |
|
|
|a Synthesis of this trisaccharide demonstrates the synthetic
|
| 520 |
|
|
|a tetrazole adduct. Glycosylations using either isomers as
|
| 520 |
|
|
|a This thesis introduces a new method of 2-deoxy glycosylation.
|
| 520 |
|
|
|a utility of glycosyl tetrazoles as potential glycosyl donors
|
| 530 |
|
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|a Also available online.
|
| 530 |
|
|
|a Issued also on microfiche from Lange Micrographics.
|
| 650 |
|
4 |
|a Major chemistry.
|
| 856 |
4 |
1 |
|u https://hdl.handle.net/1969.1/ETD-TAMU-1995-THESIS-F348
|z Link to OAKTrust copy
|t 0
|
| 999 |
|
|
|a MARS
|
| 999 |
f |
f |
|s a6c80d40-bba7-31e2-95c7-0f0ac98e0550
|i 56d74d6d-b35e-35bd-8a27-94d21a64d2c8
|t 0
|
| 952 |
f |
f |
|p noncirc
|a Texas A&M University
|b College Station
|c Cushing Memorial Library & Archives
|s cush tdrm
|d Cushing: Theses & Dissertations Microforms (Does not check out)
|t 0
|e 1995 Thesis F348
|h Other scheme
|i computer -- online resource
|
| 952 |
f |
f |
|a Texas A&M University
|b College Station
|c Electronic Resources
|s www_evans
|d Available Online
|t 0
|e 1995 Thesis F348
|h Other scheme
|
| 998 |
f |
f |
|a 1995 Thesis F348
|t 0
|l Cushing: Theses & Dissertations Microforms (Does not check out)
|
| 998 |
f |
f |
|a 1995 Thesis F348
|t 0
|l Available Online
|