About: Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes

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article by Nicos A. Petasis & Ilia A. Zavialov published November 1998 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1998 (uk) article scientifique publié en 1998 (fr) im November 1998 veröffentlichter wissenschaftlicher Artikel (de) article by Nicos A. Petasis & Ilia A. Zavialov published November 1998 in Journal of the American Chemical Society (en)
publication date	wds:Q56815724-60087DA3-E11F-437F-99CE-48C6157524DB
publication date	1998-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56815724-74CF98E7-D2F8-422E-A0E2-B441886119F6
language of work or name	English
author name string	wds:Q56815724-3CA2AE70-6324-4CB2-9C08-081C3DC0C88C wds:Q56815724-7D531EE1-34B8-40A5-A7FA-EDB9A153F71B
author name string	Nicos A. Petasis Ilia A. Zavialov
rdfs:label	Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (en) Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (nl)
skos:prefLabel	Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (en) Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (nl)
name	Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (en) Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (nl)
title	wds:Q56815724-D35F44BC-0A5F-4147-880E-6253A99BF13C
title	Highly Stereocontrolled One-Step Synthesis ofanti-β-Amino Alcohols from Organoboronic Acids, Amines, and α-Hydroxy Aldehydes (en)
page(s)	wds:Q56815724-CB8539BA-8765-4BF8-BBF7-BD80083C4EA2
page(s)	11798-11799
instance of	wds:Q56815724-C3C35BE3-C29F-4FED-B422-A22F6E07F558
instance of	scholarly article
published in	wds:Q56815724-2992BAA3-AD65-41E4-89C6-279467306169
published in	Journal of the American Chemical Society
issue	wds:Q56815724-81F0231F-E070-40B2-A5E4-43C5EA328435
volume	wds:Q56815724-945E80C2-3EC0-445B-8D8E-A58466EC38D2
issue	45
volume	120
DOI	wds:Q56815724-EB4E0AF9-958C-4AB1-AD2F-6A14F8969C00
DOI	http://dx.doi.org/10.1021/JA981075U
DOI	10.1021/JA981075U
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56815724
is cites work of	Asymmetric multicomponent reactions (AMCRs): the new frontier The Boronic Mannich Reaction in a Solid-Phase Approach Total synthesis of (±)-6-deoxycastanospermine: an application of the addition of organoboronates to N-acyliminium ions Site-specific C-functionalization of free-(NH) peptides and glycine derivatives via direct C-H bond functionalization Exploiting the borono-Mannich reaction in bioactive alkaloid synthesis Recent developments in asymmetric multicomponent reactions. Organoselenium ligands in catalysis Dual NK(1) antagonists--serotonin reuptake inhibitors as potential antidepressants. Part 2: SAR and activity of benzyloxyphenethyl piperazine derivatives Catalytic diastereoselective petasis reactions Boron and nucleic acid chemistries: merging the best of both worlds Stereocontrolled Synthesis of Quaternary β,γ-Unsaturated Amino Acids: Chain Extension of D- & L- α-(2-Tributylstannyl)Vinyl Amino Acids. Asymmetric Petasis Borono-Mannich Allylation Reactions Catalyzed by Chiral Biphenols. Multicomponent Petasis-borono Mannich Preparation of Alkylaminophenols and Antimicrobial Activity Studies Glycerol as an efficient medium for the petasis borono-mannich reaction. Synthesis of piperazinones and their apllication in constrained mimetics of the growth hormone secretagogue NN703 Synthesis of piperazinones and benzopiperazinones from 1,2-diamines and organoboronic acids One-pot three-component highly selective synthesis of homoallylboronates by using metal-free catalysis. Short synthesis of polyfunctional sp3-rich threonine-derived morpholine scaffolds. A Four-Component Reaction for the Synthesis of Dioxadiazaborocines. Synthesis, further biological evaluation and pharmacodynamics of newly discovered inhibitors of TNF-alpha production Synthesis of hyacinthacine B3 and purported hyacinthacine B7. One-step three-component reaction among organoboronic acids, amines and salicylaldehydes Synthesis of enantiopure 2-(aminoalkyl)phenol derivatives and their application as catalysts in stereoselective reactions Regioselective and Diastereoselective Allylic Amination Using Chlorosulfonyl Isocyanate. A Novel Asymmetric Synthesis of Unsaturated Aromatic 1,2-Amino Alcohols Synthesis of alpha-amino acid derivatives and amines via activation of simple alkyl halides by zinc in water Heterocyclic aldehydes as novel components in the boronic Mannich reaction The acid promoted Petasis reaction of organotrifluoroborates with imines and enamines.
is cites work of	wds:Q30558521-D99E7A2B-D6C2-4540-AB95-B90A68C6E1C6 wds:Q38094018-372FCE65-F0C9-4225-B326-15D464D0ABAF wds:Q38755880-A20F09A2-9CC2-424B-A3DF-82A961EDF058 wds:Q61632784-819CADC6-5DAD-4A39-9BF1-651DEB43ED8B wds:Q44173929-5EA27B86-FF29-4001-8342-BB8AEC401889 wds:Q42093992-CE24D1B4-0935-42D4-96A8-D84E5AADB011 wds:Q49198304-A5F0BE1C-0856-41BB-8492-5774DD900578 wds:Q44555596-FD204D26-3045-44DC-B1F6-5AB6EECC9B79 wds:Q55493799-6DD485C4-8AD0-47E3-B168-64629214DABE wds:Q81887277-05AFB46D-55CC-4DD4-9A9B-EFFF69B89554 wds:Q30054128-CF3A242D-D9A5-4DF6-9A9D-03BE3D277611 wds:Q44416140-95B1AE6F-48AA-41E3-BDEF-E4FF003557A8 wds:Q50073101-11A91947-69AB-4CDB-A932-7862FD4F39C0 wds:Q60435020-E91D3C42-5771-4185-BEE2-8208D0D3D1E8 wds:Q30047383-BA554CF4-AF9D-4D4C-8559-A2EFE59D853A wds:Q36047385-A18C7AD7-E0D1-44C2-8DB1-0686C892F570 wds:Q49692326-A4770F96-22B1-4A08-8711-2EED10A5F989 wds:Q53209817-4ED68AEA-E3C3-49FC-8DBE-622A779FA6F9 wds:Q37112461-BA094BA9-744E-49CF-B83A-162C20DDDA7D wds:Q38006603-9AA5580B-84CE-4DCD-87D7-A14521C45FCE wds:Q42645945-9E12E459-0801-41C7-A610-6F8CC79C1697 wds:Q51401538-1F52A4C6-4DC2-41A0-937A-339D9CB2B5AB wds:Q56815733-3C25E663-8A1F-4A80-AB47-1FA6FE5D7662 wds:Q43189192-3922209A-DFAB-4ACA-A35C-EA45373496C3 wds:Q44215513-491E526B-6892-4CED-9DEC-364E948BA351 wds:Q60435076-F80836EF-0EB5-4A8B-A302-25D08A055103 wds:Q61632768-95FDB261-DAA7-4606-BE10-601B66DBE20B

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