FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W4384342814> ?p ?o ?g. }

• W4384342814 endingPage "14" @default.
• W4384342814 startingPage "1" @default.
• W4384342814 abstract "Abstract This chapter describes the procedure for synthesis of [( R )‐DTBM‐SEGPHOS]NiCl 2 for the enantioselective acetal formation from N ‐Propanoyl1,3‐Thiazinane‐2‐thione and trimethyl orthoformate. It presents some of the important points to be considered, the conditions that need to be maintained, characterization data, and the reagents required, as well as the techniques used and the equipment setup that are vital to carrying out the process. The chapter also describes the hazards associated with working with chemicals and the ways to deal with these hazards. The procedures in Organic Syntheses are intended for use only by persons with proper training in experimental organic chemistry. The enantioselective and catalytic construction of carbon–carbon bonds from enolates has attracted much attention in recent years." @default.
• W4384342814 created "2023-07-15" @default.
• W4384342814 creator A5007265733 @default.
• W4384342814 creator A5037547773 @default.
• W4384342814 creator A5051810560 @default.
• W4384342814 date "2023-07-14" @default.
• W4384342814 modified "2023-09-30" @default.
• W4384342814 title "Synthesis of [( <i>R</i> )‐DTBM‐SEGPHOS]NiCl ₂ for the Enantioselective Acetal Formation from <i>N</i> ‐Propanoyl‐1,3‐Thiazinane‐2‐Thione and Trimethyl Orthoformate" @default.
• W4384342814 cites W2128830130 @default.
• W4384342814 cites W2146269918 @default.
• W4384342814 cites W2331914710 @default.
• W4384342814 cites W2509289547 @default.
• W4384342814 cites W2902578207 @default.
• W4384342814 cites W2905985796 @default.
• W4384342814 cites W2949789050 @default.
• W4384342814 cites W4253957740 @default.
• W4384342814 cites W4384627501 @default.
• W4384342814 doi "https://doi.org/10.1002/0471264229.os099.01" @default.
• W4384342814 hasPublicationYear "2023" @default.
• W4384342814 type Work @default.
• W4384342814 citedByCount "0" @default.
• W4384342814 crossrefType "other" @default.
• W4384342814 hasAuthorship W4384342814A5007265733 @default.
• W4384342814 hasAuthorship W4384342814A5037547773 @default.
• W4384342814 hasAuthorship W4384342814A5051810560 @default.
• W4384342814 hasBestOaLocation W43843428142 @default.
• W4384342814 hasConcept C146686406 @default.
• W4384342814 hasConcept C161790260 @default.
• W4384342814 hasConcept C178790620 @default.
• W4384342814 hasConcept C185592680 @default.
• W4384342814 hasConcept C21951064 @default.
• W4384342814 hasConcept C2777731525 @default.
• W4384342814 hasConcept C40875361 @default.
• W4384342814 hasConcept C41008148 @default.
• W4384342814 hasConceptScore W4384342814C146686406 @default.
• W4384342814 hasConceptScore W4384342814C161790260 @default.
• W4384342814 hasConceptScore W4384342814C178790620 @default.
• W4384342814 hasConceptScore W4384342814C185592680 @default.
• W4384342814 hasConceptScore W4384342814C21951064 @default.
• W4384342814 hasConceptScore W4384342814C2777731525 @default.
• W4384342814 hasConceptScore W4384342814C40875361 @default.
• W4384342814 hasConceptScore W4384342814C41008148 @default.
• W4384342814 hasLocation W43843428141 @default.
• W4384342814 hasLocation W43843428142 @default.
• W4384342814 hasOpenAccess W4384342814 @default.
• W4384342814 hasPrimaryLocation W43843428141 @default.
• W4384342814 hasRelatedWork W2001911836 @default.
• W4384342814 hasRelatedWork W2325654079 @default.
• W4384342814 hasRelatedWork W2748952813 @default.
• W4384342814 hasRelatedWork W2899084033 @default.
• W4384342814 hasRelatedWork W2949294999 @default.
• W4384342814 hasRelatedWork W2951775310 @default.
• W4384342814 hasRelatedWork W2952256733 @default.
• W4384342814 hasRelatedWork W2953136495 @default.
• W4384342814 hasRelatedWork W2953155228 @default.
• W4384342814 hasRelatedWork W4223993370 @default.
• W4384342814 isParatext "false" @default.
• W4384342814 isRetracted "false" @default.
• W4384342814 workType "other" @default.