author_facet Lichti, H.
von Euw, J.
Stöckel, K.
Polonia, J.
Reichstein, T.
Lichti, H.
von Euw, J.
Stöckel, K.
Polonia, J.
Reichstein, T.
author Lichti, H.
von Euw, J.
Stöckel, K.
Polonia, J.
Reichstein, T.
spellingShingle Lichti, H.
von Euw, J.
Stöckel, K.
Polonia, J.
Reichstein, T.
Helvetica Chimica Acta
Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
Inorganic Chemistry
Organic Chemistry
Physical and Theoretical Chemistry
Drug Discovery
Biochemistry
Catalysis
author_sort lichti, h.
spelling Lichti, H. von Euw, J. Stöckel, K. Polonia, J. Reichstein, T. 0018-019X 1522-2675 Wiley Inorganic Chemistry Organic Chemistry Physical and Theoretical Chemistry Drug Discovery Biochemistry Catalysis http://dx.doi.org/10.1002/hlca.19720550529 <jats:title>Abstract</jats:title><jats:p>Five crystalline compounds (anodendrosides) have been isolated from <jats:italic>Anodendron paniculatum</jats:italic> (<jats:italic>Roxb</jats:italic>.)<jats:italic>A. DC</jats:italic>. (Apocynaceae). They represent glycosides containing unusual sugars. Tentative structures for anodendroside‐A (<jats:bold>155</jats:bold>), −E<jats:sub>1</jats:sub> (<jats:bold>3</jats:bold>), −E<jats:sub>2</jats:sub> (<jats:bold>84</jats:bold>), −F (<jats:bold>144</jats:bold>) and −G (<jats:bold>115</jats:bold>) are now presented. These structures are based on UV., IR., but mostly on high resolution mass spectra. NMR.‐spectra could be performed with A, O‐acetyl‐E<jats:sub>2</jats:sub> and O‐acetyl‐G, which are in good agreement with the suggested structures. The unusual methylendioxy group postulated in the sugar moiety of A, E<jats:sub>1</jats:sub> and E<jats:sub>2</jats:sub> was also established by chemical methods, yielding approximately 1 Mol. equiv. of formaldehyde after acid hydrolysis of anodendroside‐E<jats:sub>2</jats:sub>.</jats:p> Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung Helvetica Chimica Acta
doi_str_mv 10.1002/hlca.19720550529
facet_avail Online
finc_class_facet Chemie und Pharmazie
Physik
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9obGNhLjE5NzIwNTUwNTI5
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9obGNhLjE5NzIwNTUwNTI5
institution DE-D275
DE-Bn3
DE-Brt1
DE-D161
DE-Gla1
DE-Zi4
DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
imprint Wiley, 1972
imprint_str_mv Wiley, 1972
issn 0018-019X
1522-2675
issn_str_mv 0018-019X
1522-2675
language English
mega_collection Wiley (CrossRef)
match_str lichti1972dievermutlichestrukturderanodendrosideglykosideundaglykone331mitteilung
publishDateSort 1972
publisher Wiley
recordtype ai
record_format ai
series Helvetica Chimica Acta
source_id 49
title Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_unstemmed Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_full Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_fullStr Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_full_unstemmed Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_short Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_sort die vermutliche struktur der anodendroside. glykoside und aglykone, 331. mitteilung
topic Inorganic Chemistry
Organic Chemistry
Physical and Theoretical Chemistry
Drug Discovery
Biochemistry
Catalysis
url http://dx.doi.org/10.1002/hlca.19720550529
publishDate 1972
physical 1696-1728
description <jats:title>Abstract</jats:title><jats:p>Five crystalline compounds (anodendrosides) have been isolated from <jats:italic>Anodendron paniculatum</jats:italic> (<jats:italic>Roxb</jats:italic>.)<jats:italic>A. DC</jats:italic>. (Apocynaceae). They represent glycosides containing unusual sugars. Tentative structures for anodendroside‐A (<jats:bold>155</jats:bold>), −E<jats:sub>1</jats:sub> (<jats:bold>3</jats:bold>), −E<jats:sub>2</jats:sub> (<jats:bold>84</jats:bold>), −F (<jats:bold>144</jats:bold>) and −G (<jats:bold>115</jats:bold>) are now presented. These structures are based on UV., IR., but mostly on high resolution mass spectra. NMR.‐spectra could be performed with A, O‐acetyl‐E<jats:sub>2</jats:sub> and O‐acetyl‐G, which are in good agreement with the suggested structures. The unusual methylendioxy group postulated in the sugar moiety of A, E<jats:sub>1</jats:sub> and E<jats:sub>2</jats:sub> was also established by chemical methods, yielding approximately 1 Mol. equiv. of formaldehyde after acid hydrolysis of anodendroside‐E<jats:sub>2</jats:sub>.</jats:p>
container_issue 5
container_start_page 1696
container_title Helvetica Chimica Acta
container_volume 55
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792337693893459981
geogr_code not assigned
last_indexed 2024-03-01T15:19:59.03Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Die+vermutliche+Struktur+der+Anodendroside.+Glykoside+und+Aglykone%2C+331.+Mitteilung&rft.date=1972-07-10&genre=article&issn=1522-2675&volume=55&issue=5&spage=1696&epage=1728&pages=1696-1728&jtitle=Helvetica+Chimica+Acta&atitle=Die+vermutliche+Struktur+der+Anodendroside.+Glykoside+und+Aglykone%2C+331.+Mitteilung&aulast=Reichstein&aufirst=T.&rft_id=info%3Adoi%2F10.1002%2Fhlca.19720550529&rft.language%5B0%5D=eng
SOLR
_version_ 1792337693893459981
author Lichti, H., von Euw, J., Stöckel, K., Polonia, J., Reichstein, T.
author_facet Lichti, H., von Euw, J., Stöckel, K., Polonia, J., Reichstein, T., Lichti, H., von Euw, J., Stöckel, K., Polonia, J., Reichstein, T.
author_sort lichti, h.
container_issue 5
container_start_page 1696
container_title Helvetica Chimica Acta
container_volume 55
description <jats:title>Abstract</jats:title><jats:p>Five crystalline compounds (anodendrosides) have been isolated from <jats:italic>Anodendron paniculatum</jats:italic> (<jats:italic>Roxb</jats:italic>.)<jats:italic>A. DC</jats:italic>. (Apocynaceae). They represent glycosides containing unusual sugars. Tentative structures for anodendroside‐A (<jats:bold>155</jats:bold>), −E<jats:sub>1</jats:sub> (<jats:bold>3</jats:bold>), −E<jats:sub>2</jats:sub> (<jats:bold>84</jats:bold>), −F (<jats:bold>144</jats:bold>) and −G (<jats:bold>115</jats:bold>) are now presented. These structures are based on UV., IR., but mostly on high resolution mass spectra. NMR.‐spectra could be performed with A, O‐acetyl‐E<jats:sub>2</jats:sub> and O‐acetyl‐G, which are in good agreement with the suggested structures. The unusual methylendioxy group postulated in the sugar moiety of A, E<jats:sub>1</jats:sub> and E<jats:sub>2</jats:sub> was also established by chemical methods, yielding approximately 1 Mol. equiv. of formaldehyde after acid hydrolysis of anodendroside‐E<jats:sub>2</jats:sub>.</jats:p>
doi_str_mv 10.1002/hlca.19720550529
facet_avail Online
finc_class_facet Chemie und Pharmazie, Physik
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9obGNhLjE5NzIwNTUwNTI5
imprint Wiley, 1972
imprint_str_mv Wiley, 1972
institution DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229
issn 0018-019X, 1522-2675
issn_str_mv 0018-019X, 1522-2675
language English
last_indexed 2024-03-01T15:19:59.03Z
match_str lichti1972dievermutlichestrukturderanodendrosideglykosideundaglykone331mitteilung
mega_collection Wiley (CrossRef)
physical 1696-1728
publishDate 1972
publishDateSort 1972
publisher Wiley
record_format ai
recordtype ai
series Helvetica Chimica Acta
source_id 49
spelling Lichti, H. von Euw, J. Stöckel, K. Polonia, J. Reichstein, T. 0018-019X 1522-2675 Wiley Inorganic Chemistry Organic Chemistry Physical and Theoretical Chemistry Drug Discovery Biochemistry Catalysis http://dx.doi.org/10.1002/hlca.19720550529 <jats:title>Abstract</jats:title><jats:p>Five crystalline compounds (anodendrosides) have been isolated from <jats:italic>Anodendron paniculatum</jats:italic> (<jats:italic>Roxb</jats:italic>.)<jats:italic>A. DC</jats:italic>. (Apocynaceae). They represent glycosides containing unusual sugars. Tentative structures for anodendroside‐A (<jats:bold>155</jats:bold>), −E<jats:sub>1</jats:sub> (<jats:bold>3</jats:bold>), −E<jats:sub>2</jats:sub> (<jats:bold>84</jats:bold>), −F (<jats:bold>144</jats:bold>) and −G (<jats:bold>115</jats:bold>) are now presented. These structures are based on UV., IR., but mostly on high resolution mass spectra. NMR.‐spectra could be performed with A, O‐acetyl‐E<jats:sub>2</jats:sub> and O‐acetyl‐G, which are in good agreement with the suggested structures. The unusual methylendioxy group postulated in the sugar moiety of A, E<jats:sub>1</jats:sub> and E<jats:sub>2</jats:sub> was also established by chemical methods, yielding approximately 1 Mol. equiv. of formaldehyde after acid hydrolysis of anodendroside‐E<jats:sub>2</jats:sub>.</jats:p> Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung Helvetica Chimica Acta
spellingShingle Lichti, H., von Euw, J., Stöckel, K., Polonia, J., Reichstein, T., Helvetica Chimica Acta, Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung, Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Drug Discovery, Biochemistry, Catalysis
title Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_full Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_fullStr Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_full_unstemmed Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_short Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
title_sort die vermutliche struktur der anodendroside. glykoside und aglykone, 331. mitteilung
title_unstemmed Die vermutliche Struktur der Anodendroside. Glykoside und Aglykone, 331. Mitteilung
topic Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Drug Discovery, Biochemistry, Catalysis
url http://dx.doi.org/10.1002/hlca.19720550529