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TRANS-5-TRIMETHYLSILYL-2-PENTEN-4-YN-1-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97514-97-1

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97514-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97514-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,1 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97514-97:
(7*9)+(6*7)+(5*5)+(4*1)+(3*4)+(2*9)+(1*7)=171
171 % 10 = 1
So 97514-97-1 is a valid CAS Registry Number.

97514-97-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name TRANS-5-TRIMETHYLSILYL-2-PENTEN-4-YN-1-OL

1.2 Other means of identification

Product number -
Other names (E)-5-trimethylsilanylpent-2-en-4-yn-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:97514-97-1 SDS

97514-97-1Relevant academic research and scientific papers

Cobalt-Catalyzed Diastereo- And Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates

Wang, Lei,Wang, Lifan,Li, Mingxia,Chong, Qinglei,Meng, Fanke

supporting information, p. 12755 - 12765 (2021/08/30)

Catalytic generation of ambiphilic π-allyl-metal complexes and their utility in enantioselective transformations constitutes a powerful approach for introduction of allyl groups to a molecule. Herein an unprecedented cobalt-catalyzed highly site-, diastereo-, and enantioselective protocol for stereoselective formation of nucleophilic allyl-Co(II) complexes followed by addition to aldehydes is presented. The reaction features diastereo- and enantioconvergent conversion of easily accessible allylic alcohol derivatives to diversified enantioenriched homoallylic alcohols with a remarkably broad scope of allyl groups that can be introduced. Mechanistic studies indicated that allyl radical intermediates were involved in this process. These new discoveries establish a new strategy for development of enantioselective transformations through capture of radicals by chiral Co complexes, pushing forward the frontier of Co complexes for enantioselective catalysis.

Short, Tin-Free Synthesis of All Three Inthomycins

Kumar, Manjeet,Bromhead, Liam,Anderson, Zoe,Overy, Alistair,Burton, Jonathan W.

supporting information, p. 16753 - 16756 (2018/10/26)

The inthomycins are a family of structurally and biologically rich natural products isolated from Streptomyces species. Herein the implementation of a modular synthetic route is reported that has enabled the enantioselective synthesis of all three inthomycins. Key steps include Suzuki and Sonogashira cross-couplings and an enantioselective Kiyooka aldol reaction.

Stereoselective Total Synthesis of Atractylodemayne A, a Conjugated 2(E),8(Z),10(E)-Triene-4,6-diyne

Schmidt, Bernd,Aud?rsch, Stephan

supporting information, p. 1162 - 1165 (2016/03/15)

The first total synthesis of the polyacetylene natural product atractylodemayne A is reported. Stereoselective construction of the conjugated 8(Z),10(E)-diene moiety was achieved through a tethered ring-closing metathesis approach, comprising a Ru-catalyz

Synthesis of hydroxylated pyrrolidines by allenic cyclisation

Ng, Pearly Shuyi,Bates, Roderick W.

, p. 6356 - 6362 (2016/09/23)

The diastereoselective gold(I) catalysed cyclisation of highly substituted aminoallene derivatives allows the synthesis of both epi-DAB-1 and di-epi-lentiginosine. While the sense of stereoselectivity observed is in line with earlier observations on analo

A convergent approach to (-)-callystatin a based on local symmetry

Candy, Mathieu,Tomas, Lo?c,Parat, Sabrina,Heran, Virginie,Bienaymé, Hugues,Pons, Jean-Marc,Bressy, Cyril

supporting information, p. 14267 - 14271 (2013/01/15)

The key is symmetry! A convergent synthetic approach of the highly cytotoxic natural product (-)-callystatin A was developed assembling three fragments through Julia-Kocienski olefination and Stille cross-coupling. The new strategy relies on a pivotal local symmetry of the target molecule. In this preliminary study, particular attention was devoted to facilitate the catalytic enantiocontrol of strategic stereogenic centers present in each of the fragments (see scheme). Copyright

Total synthesis of fostriecin: Via a regio-and stereoselective polyene hydration, oxidation, and hydroboration sequence

Gao, Dong,O'doherty, George A.

supporting information; experimental part, p. 3752 - 3755 (2010/12/18)

A total synthesis of the fostriecin has been achieved in 24 steps from enyne 11. The lactone moiety was installed by a Leighton allylation and Grubbs ring-closing metathesis reaction. The highly reactive Z,Z,E-triene moiety was installed via a late-stage Suzuki-Miyaura cross-coupling of a remarkably stable Z-vinyl boronate. The relative and absolute stereocenters of the C-8,9,11 triol were generated with a regio-and stereoselective asymmetric hydration/oxidation sequence.

Synthesis of isomeric polyacetylenes based on natural hydroxy matricaria esters

Garrais, Solange,Turkington, Jennifer,Goldring, William P.D.

experimental part, p. 8418 - 8427 (2009/12/26)

The construction of a library of natural and related polyacetylenes using a convergent synthetic strategy based on a palladium mediated cross-coupling reaction is described. The systematic synthetic study led to all possible alkene isomers of the hydroxy matricaria esters 29-32, and the corresponding tiglates 1-4. The synthesis of many of these compounds is described for the first time.

Highly regioselective decarboxylative Claisen rearrangement reactions of diallyl 2-sulfonylmalonates

Craig, Donald,Lansdell, Mark I.,Lewis, Simon E.

, p. 7861 - 7864 (2008/03/11)

The decarboxylative Claisen rearrangement of a range of substituted diallyl 2-sulfonylmalonates is described. The substrates are made by C-carboxylation of the corresponding allyl sulfonylacetates with allyl para-nitrophenyl carbonates. The reactions display a high degree of regioselectivity, with allylic substituents possessing electron-rich substituents at the allyl three-position rearranging preferentially.

Ru-catalyzed alkene-alkyne coupling. Total synthesis of amphidinolide P

Trost, Barry M.,Papillon, Julien P. N.,Nussbaumer, Thomas

, p. 17921 - 17937 (2007/10/03)

A coordinatively unsaturated ruthenium complex catalyzed the formation of a carbon-carbon bond between two judiciously chosen alkene and alkyne partners in good yield, and in a chemo- and regioselective fashion, despite the significant degree of unsaturation of the substrates. The resulting 1,4-diene forms the backbone of the cytotoxic marine natural product amphidinolide P. The alkene partner was rapidly assembled from (R)-glycidyl tosylate, which served as a linchpin in a one-flask, sequential three-components coupling process using vinyllithium and a vinyl cyanocuprate. The synthesis of the alkyne partner made use of an unusual anti-selective addition under chelation-control conditions of an allyltin reagent derived from tiglic acid. In addition, a remarkably E-selective E2 process using the azodicarboxylate-triphenylphosphine system is featured. Also featured is the first example of the use of a β-lactone as a thermodynamic spring to effect macrolactonization. The oxetanone ring was thus used as a productive protecting group that increased the overall efficiency of this total synthesis. This work was also an opportunity to further probe the scope of the ruthenium-catalyzed alkene-alkyne coupling, in particular using enynes, and studies using various functionalized substrates are described.

Synthesis of methyl (5S,6R,7E,9E,11Z,13E,15S)-16-(4-fluorophenoxy)-5,6,15-trihydroxy-7,9,11, 13-hexadecatetraenoate, an analogue of 15R-lipoxin A4

Phillips, Eifion D.,Chang, Hui-Fang,Holmquist, Christopher R.,McCauley, John P.

, p. 3223 - 3226 (2007/10/03)

We describe a method for the synthesis of methyl (5S,6R,7E,9E,11Z,13E,15S)-16-(4-fluorophenoxy)-5,6,15-trihydroxy-7,9,11, 13-hexadecatetraenoate, a compound that has been described as a metabolically stable analogue of 15R-lipoxin A4.

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