ChemInform Abstract: Convenient Glycoside Synthesis of Amino Sugars: Michael-Type Addition to 2-Nitro-D-galactal.

J. DAS; R. R. SCHMIDT

doi:10.1002/chin.199848237

ChemInform Abstract: Convenient Glycoside Synthesis of Amino Sugars: Michael-Type Addition to 2-Nitro-D-galactal.

ChemInform ◽

10.1002/chin.199848237 ◽

2010 ◽

Vol 29 (48) ◽

pp. no-no

Author(s):

J. DAS ◽

R. R. SCHMIDT

Keyword(s):

Amino Sugars ◽

Glycoside Synthesis ◽

Michael Type Addition

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Convenient Glycoside Synthesis of Amino Sugars: Michael-Type Addition to 2-Nitro-D-galactal

European Journal of Organic Chemistry ◽

10.1002/(sici)1099-0690(199808)1998:8<1609::aid-ejoc1609>3.0.co;2-1 ◽

1998 ◽

Vol 1998 (8) ◽

pp. 1609-1613 ◽

Cited By ~ 42

Author(s):

Jagattaran Das ◽

Richard R. Schmidt

Keyword(s):

Amino Sugars ◽

Glycoside Synthesis ◽

Michael Type Addition

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Photosensitive protecting groups of amino sugars and their use in glycoside synthesis. 2-Nitrobenzyloxycarbonylamino and 6-nitroveratryloxycarbonylamino derivatives

The Journal of Organic Chemistry ◽

10.1021/jo00916a015 ◽

1974 ◽

Vol 39 (2) ◽

pp. 192-196 ◽

Cited By ~ 73

Author(s):

Boaz Amit ◽

Uri Zehavi ◽

Abraham Patchornik

Keyword(s):

Protecting Groups ◽

Amino Sugars ◽

Glycoside Synthesis

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ChemInform Abstract: PHOTOSENSITIVE PROTECTING GROUPS OF AMINO SUGARS AND THEIR USE IN GLYCOSIDE SYNTHESIS, 2-NITROBENZYLOXYCARBONYLAMINO AND 6-NITROVERATRYLOXYCARBONYLAMINO DERIVATIVES

Chemischer Informationsdienst ◽

10.1002/chin.197418448 ◽

1974 ◽

Vol 5 (18) ◽

pp. no-no

Author(s):

B. AMIT ◽

U. ZEHAVI ◽

A. PATCHORNIK

Keyword(s):

Protecting Groups ◽

Amino Sugars ◽

Glycoside Synthesis

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Rare amino sugars in exopolysaccharides (EPS) from cyanobacteria of the genus Synechocystis

Planta Medica ◽

10.1055/s-0030-1264463 ◽

2010 ◽

Vol 76 (12) ◽

Author(s):

D Flamm ◽

W Blaschek

Keyword(s):

Amino Sugars

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Faculty Opinions recommendation of Evidence that intracellular stages of Leishmania major utilize amino sugars as a major carbon source.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.7562956.8890069 ◽

2011 ◽

Author(s):

Marilyn Parsons

Keyword(s):

Carbon Source ◽

Leishmania Major ◽

Amino Sugars

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Amino sugars. X. Preparation of 3-amino-3,6-dideoxy-D-gulose, -D-allose and -L-allose derivatives

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19662558 ◽

1966 ◽

Vol 31 (6) ◽

pp. 2558-2564 ◽

Cited By ~ 7

Author(s):

K. Čapek ◽

J. Jarý

Keyword(s):

Amino Sugars

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Amino sugars. XXVI. Preparation of derivatives of 3-amino-3,4,6-trideoxy-D-arabino-hexopyranose

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19720484 ◽

1972 ◽

Vol 37 (2) ◽

pp. 484-492 ◽

Cited By ~ 1

Author(s):

K. Čapek ◽

J. Jarý

Keyword(s):

Amino Sugars ◽

Derivatives Of

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Amino sugars. XXVII. The synthesis of derivatives of 3-amino-3,4,6-trideoxy-D- or L-xylo-hexopyranose

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19722985 ◽

1972 ◽

Vol 37 (9) ◽

pp. 2985-2993 ◽

Cited By ~ 5

Author(s):

K. Kefurt ◽

K. Čapek ◽

J. Čapková ◽

Z. Kefurtová ◽

J. Jarý

Keyword(s):

Amino Sugars ◽

Derivatives Of

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Amino sugars. XVI. Partial acetylation and deacetylation of methyl 3-acetamido-3,6-dideoxy-α-L-idopyranoside derivatives

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19680781 ◽

1968 ◽

Vol 33 (3) ◽

pp. 781-787 ◽

Cited By ~ 5

Author(s):

K. Čapek ◽

J. Šteffková ◽

J. Jarý

Keyword(s):

Amino Sugars

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Amino sugars. XV. Synthesis of derivatives of 3,6-diamino-3,6-dideoxy-L-talose

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19680549 ◽

1968 ◽

Vol 33 (2) ◽

pp. 549-555 ◽

Cited By ~ 9

Author(s):

J. Kovář ◽

J. Jarý

Keyword(s):

Amino Sugars ◽

Derivatives Of

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