About: Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin

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article by R. B. Woodward et al published June 1981 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1981 (uk) article scientifique publié en 1981 (fr) im Juni 1981 veröffentlichter wissenschaftlicher Artikel (de) article by R. B. Woodward et al published June 1981 in Journal of the American Chemical Society (en)
publication date	wds:Q56047811-0FFD9691-B8DE-4CFB-B01A-50C38648DF7D
publication date	1981-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56047811-AC5197C3-EFB4-4086-886A-635872668270
language of work or name	English
author name string	wds:Q56047811-0B514F8A-64F8-4091-BB70-7C9F534C76DD wds:Q56047811-1B2E2BF9-1AA2-4560-BE60-0039C60BBECB wds:Q56047811-4AC25969-B854-4B00-A3B4-5AE984FD1D6B wds:Q56047811-51E1CF6A-7C59-4D18-818F-CCD19CB71295 wds:Q56047811-BA6DA0D6-8E51-44A5-A0DB-1FB4BC30C873 wds:Q56047811-BDA5212E-656D-4873-808D-14BBD1F1156F wds:Q56047811-CCB5B816-7C94-4109-98DB-C6D1716690B6 wds:Q56047811-CD5D1144-B407-4CC4-8C50-31865517C7FF wds:Q56047811-E34306CE-E68C-4C61-8B3E-39D7AA0F04C5 wds:Q56047811-E833BEA4-E611-42FB-BEBA-46E579D9E523
author name string	D. E. Ward C. H. Chen P. Balaram R. B. Woodward L. J. Browne P. J. Card B. W. Au-Yeung E. Logusch K. P. Nambiar K. Sakan
rdfs:label	Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (en) Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (nl)
skos:prefLabel	Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (en) Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (nl)
name	Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (en) Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (nl)
title	wds:Q56047811-303C94B2-45B0-4394-99A0-A87FA5659D04
title	Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin (en)
page(s)	wds:Q56047811-F3D10728-1226-4BF5-B121-A012B8A2D405
page(s)	3215-3217
instance of	wds:Q56047811-036F0060-7B89-42C2-8F53-D06A0FCF827C
instance of	scholarly article
main subject	wds:Q56047811-BE8784C0-EAE9-43FB-9162-67A934B46B3F
main subject	wd:Q213511
published in	wds:Q56047811-B5F8E076-3748-411C-8C6B-6B23482320C5
published in	Journal of the American Chemical Society
issue	wds:Q56047811-B2566651-4A54-44AF-A821-37A1A056E549
volume	wds:Q56047811-72EC6E67-777F-4B2F-8785-C665E72AE715
issue	11
volume	103
DOI	wds:Q56047811-D7177F64-A046-4EA5-99B2-98BBD79BAB52
DOI	http://dx.doi.org/10.1021/JA00401A051
DOI	10.1021/JA00401A051
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56047811
is cites work of	Anomeric-oxygen activation for glycoside synthesis: the trichloroacetimidate method A platform for the discovery of new macrolide antibiotics. Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products. Thioglycosides as glycosyl donors in oligosaccharide synthesis. O-Glycosylation methods in the total synthesis of complex natural glycosides Efficient intramolecular beta-mannoside formation using m-xylylene and isophthaloyl derivatives as rigid spacers. Synthesis and reactions of glycosides The Quest for Quinine: Those Who Won the Battles and Those Who Won the War The macrolide antibiotic renaissance Asymmetric Assembly of All-Carbon Tertiary/Quaternary Nonadjacent Stereocenters through Organocatalytic Conjugate Addition of α-Cyanoacetates to a Methacrylate Equivalent. Trends in applying C-H oxidation to the total synthesis of natural products Toward the ideal synthesis and molecular function through synthesis-informed design A brief history of antibiotics and select advances in their synthesis The thiopyran route to polypropionates Synthesis of Antibiotics Crystal structure of (6E,20E)-3,24-di-fluoro-13,14,28,29-tetra-hydro-5H,22H-tetra-benzo[e,j,p,u][1,4,12,15]tetra-oxa-cyclo-docosine-5,22-dione Synthesis of D-Desosamine and Analogs by Rapid Assembly of 3-Amino Sugars. Lessons from the synthetic chemist nature Nature nurtures the design of new semi-synthetic macrolide antibiotics Large-scale preparation of key building blocks for the manufacture of fully synthetic macrolide antibiotics. Glycosylation of an allenic erythronolide
is cites work of	wds:Q35988337-78754408-6DD7-4C6B-A66D-983BAC2B3951 wds:Q39406507-8E022938-2D1D-42C1-B07A-E103283F1815 wds:Q38972486-854F9CB4-C274-4429-B950-AC9FBE46A9AE wds:Q38723563-2FBE975C-F066-44EA-A195-A323165E3D2D wds:Q37901401-31B8A6F1-1B73-4E43-9477-235BA3D72C3D wds:Q38525726-51EF9EA5-11CF-4A26-9CF3-051B967885B2 wds:Q37554629-73916426-E959-4879-816B-5F2427A8EFF2 wds:Q39414195-9B5610C4-0368-43C7-9985-5B9673907A8C wds:Q43885998-38D9F5E2-8062-458B-A0A7-869FA833DAE4 wds:Q38366491-5F48FC56-242D-4C82-BA49-B9C1826660A0 wds:Q48129484-FEF33BC0-C945-463F-9E5F-1961D47524D0 wds:Q50091487-274639F5-E34B-4E4A-9253-29F419D4C5C5 wds:Q72759073-082D1218-5577-490C-896B-FFB7C291D880 wds:Q21032515-5AEB1335-9163-434C-B281-5261708030B3 wds:Q36021739-8DD3E56E-3D05-4594-9B3D-3AFA94B763B1 wds:Q50907857-E4843AAD-8416-4A48-A0D3-4404F79CD11F wds:Q41527986-BF056DAF-1BB9-40FE-91FB-4AEA2A5192B6 wds:Q91997779-6B0904D0-70A7-410D-B547-6F52D8F5E3F7 wds:Q30650504-F4B29804-F356-47C9-BC9F-D2C71B5EDC15 wds:Q38192884-970AB2F0-2A9C-43F6-878D-DBD5340A718E wds:Q39023947-23FFF8C3-8904-4DB1-8430-B1FA18BE20C7

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