About: Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides

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About: Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) ലേഖനം (ml) հոդված (hy) wetenschappelijk artikel (nl) наукова стаття, опублікована в 1969 (uk) im Jahr 1969 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56529519-4FB82679-4D2A-460D-886E-29BC065BBE31
publication date	1969-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q56529519-64AB3B90-8F5C-453F-A4A2-12329798D7B9 wds:Q56529519-7712AB2A-DE4A-4615-8DF1-153E7BAA65A1
author name string	R. J. Ferrier N. Prasad
rdfs:label	Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (en) Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (nl)
skos:prefLabel	Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (en) Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (nl)
name	Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (en) Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (nl)
title	wds:Q56529519-14F022AA-AFF3-4524-B02C-28E54D84C458
title	Unsaturated carbohydrates. Part X. Epoxidations and hydroxylations of 2,3-dideoxy-α-D-hex-2-enopyranosides. The four methyl 4,6-di-O-acetyl-2,3-anhydro-α-D-hexopyranosides (en)
page(s)	wds:Q56529519-1F531DB4-F723-4A7B-B70A-1ED40C31BBC1
page(s)	575-580
instance of	wds:Q56529519-648405AB-D128-42A8-A3EF-978F6CD75AC2
instance of	scholarly article
published in	wds:Q56529519-DC204068-3238-4480-937E-16F9F0C7C6A9
published in	Journal of the Chemical Society. C, Organic
issue	wds:Q56529519-9155939D-97E5-4EED-837A-BE4A221F5D43
volume	wds:Q56529519-27FFB41F-7EB6-458D-850A-4946F68A4C15
issue	4
volume	0
DOI	wds:Q56529519-C678A865-222B-44A8-9E2A-9D4042775D2C
DOI	http://dx.doi.org/10.1039/J39690000575
DOI	10.1039/J39690000575
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56529519
is cites work of	Synthesis of methyl 2,3-dideoxy-DL-alk-2-enopyranosides from furan compounds Allylic rearrangement of 6-deoxyglycals having practical utility. Stereoselective total synthesis of methyl alpha-D and alpha-L-glucopyranosides Epoxidation and bis-hydroxylation of C-phenyl-delta(2,3)-glycopyranosides. A Survey of Recent Synthetic Applications of 2,3-Dideoxy-Hex-2-enopyranosides Isolation and characterization of an unsubstituted 2,3-unsaturated sugar, trans-2,3-dideoxy-d-glycero-pent-2-enose, produced by thermal dehydration of 2-deoxy-d-erythro-pentose
is cites work of	wds:Q46897086-59432930-D3C6-4758-A0BC-94BF208E5034 wds:Q56586560-2E6C6F80-B20C-46AC-8856-14B6F6E71E4A wds:Q43868368-0CEE52FF-AD50-44C3-9A42-5BEFEC0219EC wds:Q39063354-E86E7D5C-4768-4871-A982-E1444809EB79 wds:Q53825160-BE128CAA-6FF5-472D-BA7E-BFFF132DBAFC wds:Q26851777-18ACA52C-9B75-4E09-8ADD-682EE65C35A1

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