Glycosyl tetrazoles as glycosyl donors for the synthesis of 2-deoxy glycosides /

2-Deoxy oligosaccharides form a major component of

Bibliographic Details
Main Author: Falahatpisheh, Nikoo
Format: Thesis eBook
Language:English
Published: [Place of publication not identified] : [publisher not identified] ; 1995.
Subjects:
Online Access:Link to OAKTrust copy

MARC

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007 cr unu a
008 960813s1995 xx a b 000 0 eng d
035 |9 AHB7886AM 
035 |a (OCoLC)35231020 
040 |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 |a Includes bibliographical references. 
520 |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 |a biologically active aureolic acid and angucycline  
520 |a butylphosphoramidite produces N2 and N1 isomer of the  
520 |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 |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