About: Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds

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scholarly article by Toshimichi Ohmura et al published May 2000 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2000 (uk) article scientifique publié en 2000 (fr) im Mai 2000 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Toshimichi Ohmura et al published May 2000 in Journal of the American Chemical Society (en)
publication date	wds:Q57713860-129DF34F-CCFD-4550-AAD5-3A6A39767F97
publication date	2000-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57713860-218A73B5-71E9-418C-B6F2-625FC8BB7EF4
language of work or name	English
cites work	wds:Q57713860-316A7630-1A67-478D-914D-858E44034455 wds:Q57713860-C8DDB3DE-5876-4B5E-BD94-0AAF7FCAE8B6
cites work	Convenient Routes to Vinylideneruthenium Dichlorides with Basic and Bulky Tertiary Phosphine Ligands (PPrᶦ₃ and PCy₃) Five-Coordinate 16-Electron Carbene- and Vinylideneruthenium(II) Complexes Prepared from [RuCl₂(C₈>H₁₂)]ₙ or from the New Dihydridoruthenium(IV) Compound [RuH₂Cl₂(PᶦPr₃)₂]
author name string	wds:Q57713860-C5C07D15-C978-4F13-9D4C-6E311A0AC775
author name string	Toshimichi Ohmura
rdfs:label	Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (en) Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (nl)
skos:prefLabel	Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (en) Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (nl)
name	Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (en) Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (nl)
author	wds:Q57713860-243A1A34-C82B-4182-B5B8-E50C8E84A5F1 wds:Q57713860-69388DD8-42D5-4E96-BE28-BB479F8FCC98
author	Norio Miyaura Yasunori Yamamoto
title	wds:Q57713860-8C854E6D-9C6D-478E-B9C6-BC31FBA6372A
title	Rhodium- or Iridium-Catalyzedtrans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds (en)
page(s)	wds:Q57713860-84A20332-2D4B-4430-BDEA-774B1E23AEF3
page(s)	4990-4991
instance of	wds:Q57713860-EEAA678C-DB05-429B-8F84-C52F99EB0EF2
instance of	scholarly article
main subject	wds:Q57713860-E3DB7573-B7AD-4913-96F5-63AE573A4F3F wds:Q57713860-a24bf13b-67eb-4204-8a8a-77fd544173e8
main subject	rhodium iridium
published in	wds:Q57713860-4CA6FC77-8261-4C7B-8175-76F13CAA9AA3
published in	Journal of the American Chemical Society
issue	wds:Q57713860-E7A8F30A-5FDC-46AD-A7B9-3EA86474D735
volume	wds:Q57713860-D2605327-5767-4078-BC92-98D0609C830E
issue	20
volume	122
DOI	wds:Q57713860-0E1AB5E7-1B91-49FF-9FA2-7FCD881DA2DB
DOI	http://dx.doi.org/10.1021/JA0002823
DOI	10.1021/JA0002823
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57713860
is cites work of	Synthesis of Z-(pinacolato)allylboron and Z-(pinacolato)alkenylboron compounds through stereoselective catalytic cross-metathesis Selection of boron reagents for Suzuki-Miyaura coupling. Electronic influence of β-diketonato-type ligands on the coordination of 1,5-cyclooctadiene to palladium(II) as defined by 'Venus fly trap' geometric parameters Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis An alkene-promoted borane-catalyzed highly stereoselective hydrogenation of alkynes to give Z- and E-alkenes. A trans-selective hydroboration of internal alkynes. (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol: Valuable reagent in the asymmetric synthesis of organoboronates Lewis acid catalysis: catalytic hydroboration of alkynes initiated by Piers' borane Mechanism and Origin of the Stereoselectivity in the Palladium-Catalyzed trans Hydroboration of Internal 1,3-Enynes with an Azaborine-Based Phosphine Ligand. Total Synthesis and Biological Assessment of (−)-Exiguolide and Analogues Earth-Abundant Transition Metal Catalysts for Alkene Hydrosilylation and Hydroboration: Opportunities and Assessments A masked diboron in Cu-catalysed borylation reaction: highly regioselective formal hydroboration of alkynes for synthesis of branched alkenylborons. Synergy of synthesis, computation and NMR reveals correct baulamycin structures. Copper-Catalyzed Transformations Using Cu-H, Cu-B, and Cu-Si as Active Catalyst Species Boryl substitution of functionalized aryl-, heteroaryl- and alkenyl halides with silylborane and an alkoxy base: expanded scope and mechanistic studies. Tris(2,4,6-trifluorophenyl)borane: An Efficient Hydroboration Catalyst.
is cites work of	wds:Q46859296-89B2AE03-CB40-4706-A36D-7E27700EADB4 wds:Q58071950-DFDC3056-6A43-40C0-BA4A-F6A04D140217 wds:Q46515281-4269AC73-C80E-4E69-B594-D19E520074CB wds:Q47412442-1FB9DCD4-00E9-4EF9-A050-E5519B92BA74 wds:Q38887365-BC275FA7-D162-4F3C-96DA-97AF96F75B1D wds:Q54671407-9FA185C7-318F-417C-9CBE-0A6DBB35BB8E wds:Q51562219-520D0663-7FD3-4AC2-AF61-BD11DCF170B6 wds:Q51017747-F7A285AB-7D01-4701-997B-5E13B2BF70F6 wds:Q57521127-2E2CDB63-C526-4322-885F-BFBEA1B303EC wds:Q53575592-83039C1F-564F-424D-9230-EC1424698C1C wds:Q91443559-4719136D-4CAB-42D0-A7F7-CEEC0751670F wds:Q40581007-4260FFC6-9507-4FFB-81C6-276A84684084 wds:Q41569025-4CC341CC-6099-43C6-81F2-2F4370168D1C wds:Q38148935-5E61CDE1-60F3-40DE-91CB-78B3B6F04C80 wds:Q29306760-B01A1D59-ED89-45E2-A6E8-DEDBBF3E7AA6 wds:Q47193906-727E1A44-55BF-45AD-8089-25F15054879D

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