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1. |
Letter of Introduction |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 1-1
Atta-ur-rahman,
Ernest Wenkert,
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ISSN:1057-5634
DOI:10.1080/10575639208048876
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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2. |
The Synthesis of 2′-Deoxyguanosines Having an Arylamino Group At the C-8 Position |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 3-7
Chin-Yi Huang,
Francis Johnson,
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摘要:
A general route is described for the synthesis of 8-arylamino derivatives of 2′-deoxyguanosine. the method takes advantage of (a) the far greater stability of the ribonucleoside series to acid conditions during the introduction of the aminoaryl group and (b) a modified form of Barton's radical deoxygenation procedure to remove the 2′-hydroxyl group. the synthetic pathway allows the preparation of the desired materials on a gram scale and avoids the use of an ultimate carcinogen as an intermediate.
ISSN:1057-5634
DOI:10.1080/10575639208048877
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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3. |
A Novel Azotobactin From Azotobacter Vinelandii |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 9-14
H. Budzikiewicz,
E.M. Schaffner,
K. Taraz,
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摘要:
From cultures ofAzotobacter vinelandiiDSM 87 (ATCC 12837) an azotobactin was isolated and its structure was elucidated by MS, NMR, and chemical degradation studies. This is the second representative of its class of bacterial siderophores so far encountered. of special interest also in respect of the relatedPseudomonassiderophores (pyoverdins) is a novel hydroxamic acid unit (N5-hydroxy-N5-hydroxybutyryl-ornithine) as one of the binding sites for Fe3+.
ISSN:1057-5634
DOI:10.1080/10575639208048878
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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4. |
Studies On the Synthesis of Mavacurine Type Alkaloids. Synthesis of 6a-Homopleiocarpamine |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 15-19
M.-Lluisa Bennasar,
Ester Zulaica,
Juan-Miguel Jimenez,
Joan Bosch,
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摘要:
Closure of the six-membered C ring of pentacyclic mavacurine type alkaloids, by formation of either C6-C7or N4-C5bonds, failed. In contrast, 6a-homopleiocarpamine has been synthesized using as the key step an electrophilic cyclization upon the indole 3-position (bond formed C6a-C7) from an appropriately substituted tetracyclic derivative having a three-carbon chain on the piperidine nitrogen.
ISSN:1057-5634
DOI:10.1080/10575639208048879
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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5. |
Facile Synthesis of (2S,3R)-3-Amino-2-Hydroxycarboxylic Acids, the Key Components of Amastatin and Bestatin |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 21-24
Seigo Ishibuchi,
Takeshi Nagatani,
Tadao Ishizuka,
Takehisa Kunieda,
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摘要:
The title amino acids, (2S,3R)-3-amino-2-hydroxy-5-methyl-hexanoic acid (AHMHA) and (2S,3R)-3-amino-2-hydroxy-4-phenylbutanoic acid (AHPBA), are stereoselectively prepared from (4R,5R)-5-allyl-4-methoxy-2-oxazolidinone which is readily accessible from the previously reported chiral synthon, (4R,5R)-5-phenylseleno-4-methoxy-2-oxazolidinone.
ISSN:1057-5634
DOI:10.1080/10575639208048880
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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6. |
RegioselectiveO-Methylation of Hydroxyl GroupsVia1,3-Benzodithiol-2-Yl Ether Intermediates |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 25-28
Mitsuo Sekine,
Takeshi Nakanishi,
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摘要:
A two-step regioselectiveO-methylation of hydroxyl groupsvia1,3-benzodithiol ether intermediates has been developed. theO-alkylation of alcohols containing a phenolic hydroxyl group or pyridine skeleton was successfully performed.
ISSN:1057-5634
DOI:10.1080/10575639208048881
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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7. |
Biologically Active Metabolites From Fungi, 21an Antifungal and Herbicidal Lanostane Lactone FromSporormiella Australis |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 29-32
Karsten Krohn,
Kerstin Ludewig,
PeterG. Jones,
Detlev Döring,
Hans-Jügen Aust,
Siegfried Draeger,
Barbara Schulz,
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摘要:
A new herbicidal lanostane lactone (1) has been isolated fromSporormiella australis.
ISSN:1057-5634
DOI:10.1080/10575639208048882
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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8. |
Potent Inhibition of Neuraminidase By N-(1,2-Dihydroxypropyl) Derivatives of Siastatin B and Its Analogs |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 33-38
Yoshio Nishimura,
Toshiaki Kudo,
Yoji Umezawa,
Shinichi Kondo,
Tomio Takeuchi,
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摘要:
Inhibitors, reaction intermediates and substrate analogs of neuramic acid were studied by molecular graphics. Based on this chemically modified analogs of siastatin B, an inhibitor of neuraminidases were synthesized. the results indicated that potent inhibitors must be good topographical analogs of the oxocarbenium ion of neuraminic acid, an intermediate in the reaction catalyzed by neuraminidase.
ISSN:1057-5634
DOI:10.1080/10575639208048883
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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9. |
Design of Potential Neuraminidase Inhibitors By Dehydration, Deoxygenation and Epimerization of Siastatin B |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 39-44
Yoshio Nishimura,
Toshiaki Kudo,
Yoji Umezawa,
Shinichi Kondo,
Tomio Takeuchi,
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摘要:
Rationally designed analogs of siastatin B able to mimic oxocarbenium ion of neuraminic acid, an intermediate in the reaction catalyzed by the enzyme, were synthesized. Those types represented the improvement over siastatin B.
ISSN:1057-5634
DOI:10.1080/10575639208048884
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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10. |
Synthesis of PorphyrinC-Glycoconjugates |
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Natural Product Letters,
Volume 1,
Issue 1,
1992,
Page 45-50
Giovanni Casiraghi,
Mara Cornia,
Gloria Rassu,
CarloDel Sante,
Pietro Spanu,
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摘要:
Two novel chiral porphyrins (5) and (7), with two and four alditolyl chains attached at the bridging methine carbons, have been synthesized via, respectively, coupling of the dipyrryl unit (3) with p-fluorobenzaldehyde (4) and BF3-catalyzed condensation between pyrrole and 2,3-O-isopropylidene-D-glyceraldehyde (6).
ISSN:1057-5634
DOI:10.1080/10575639208048885
出版商:Taylor & Francis Group
年代:1992
数据来源: Taylor
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