About: Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration

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About: Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1972 (uk) im Juni 1972 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56192398-ED4AE0FB-90BD-43A1-A4FF-7964D5F89726
publication date	1972-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56192398-3D3375CE-40F8-4D12-874A-378A25432F16
language of work or name	English
author name string	wds:Q56192398-1A2EDFBE-CA61-4D1B-8CB4-2DAC4A6509F5 wds:Q56192398-F607AA33-F045-490A-85F4-2A6F21896ED0
author name string	S. K. Gupta Herbert C. Brown
rdfs:label	Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (en) Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (nl)
skos:prefLabel	Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (en) Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (nl)
name	Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (en) Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (nl)
title	wds:Q56192398-B89A4204-32C6-422F-86DF-043F1F2E1AE8
title	Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration (en)
page(s)	wds:Q56192398-4CD2BEAF-4ECD-4566-80F3-FBA76D879A0B
page(s)	4370-4371
instance of	wds:Q56192398-32A05353-CE29-403C-8CC3-B1C7BA4529FE
instance of	scholarly article
published in	wds:Q56192398-CAA90954-76B2-4552-80C6-49DD1E88DAD6
published in	Journal of the American Chemical Society
issue	wds:Q56192398-A365A641-1892-4077-9C75-62E1011E8F28
volume	wds:Q56192398-C348C025-BC8E-4A27-B536-400A1AA150DD
issue	12
volume	94
DOI	wds:Q56192398-0E31A89A-1C18-4692-9496-0F85CFE35342
DOI	http://dx.doi.org/10.1021/JA00767A072
DOI	10.1021/JA00767A072
Fatcat ID	wds:Q56192398-13FF22DD-3C25-4720-A9CB-C5D94F95D517
Fatcat ID	release_fmi2zppk4fehngf2cdleb5rbly
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56192398
is cites work of	New anacardic acid-inspired benzamides: histone lysine acetyltransferase activators The boronic acid mannich reaction: A new method for the synthesis of geometrically pure allylamines Synthesis of 2-keto-anti-1,3-diols by chemoselective tandem oxidation of 2-B(pin)-substituted allylic alcohols. Isolation, structural determination and synthetic approaches toward amphidinol 3. Iridium-catalyzed, diastereoselective dehydrogenative silylation of terminal alkenes with (TMSO)2MeSiH. Photo-driven anti-Markovnikov alkyne hydration in self-assembled hollow complexes. Boron and nitrogen co-doped ordered microporous carbons with high surface areas The Negishi Cross-Coupling in the Synthesis of Natural Products and Bioactive Molecules Copper-Catalyzed Transformations Using Cu-H, Cu-B, and Cu-Si as Active Catalyst Species Synthesis of Alkenylboronic Esters: An Alternative Route to Trisubstituted Homoallylic Alcohols New stereospecific syntheses of pheromone bombykol and its three geometrical isomers A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes Stereocontrolled synthesis of carbon–carbon double bond locked analogues of strobilurins which are characterized by a trans-1,2-disubstituted cyclopropane ring Rhodium(I) catalysed diboration of (E)-styrylboronate esters: molecular structures of (E)-p-MeO–C6H4–CHCH–B(1,2-O2C6H4) and p-MeO–C6H4–CH2C{B(1,2-O2C6H4)}3
is cites work of	wds:Q46557966-33A9520D-6EE6-4338-8456-0335CE2807C0 wds:Q57715325-967BE224-416D-4A02-8E5E-90F5D64776ED wds:Q58101062-06596774-2370-4970-BAA2-1511A752DEE8 wds:Q38887365-12745126-BDBE-49A8-8060-55F3E0698927 wds:Q38188454-AA63B087-44F6-4BB6-B56C-29FFC6AB7918 wds:Q58071706-7E822403-A1E4-42AA-B0CE-12ED5658F82D wds:Q59345692-FFCCB8FC-BC94-488B-9DC5-62B24E611157 wds:Q63309531-81291FB1-EFB2-49E7-B686-308A6227BA8C wds:Q29027294-18A85BE0-3BD4-4B95-BA59-E7DFEEE526D4 wds:Q60318637-790793C9-E000-4AB7-852D-47AD7AEF640C wds:Q62396307-7529D759-DF1A-442C-A5F5-E67BA29A38BF wds:Q39671625-7A8E7DEE-134C-4E45-AAFF-756937C957AC wds:Q53203523-B68908DB-5055-4853-B60C-705EAE061439 wds:Q54750571-6F8A04A1-8C27-4630-816C-F709DF6B44F4

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