Sodium Bis(2-methoxyethoxy)aluminum Hydride - Wikidata - wikimedia - TriplyDB

Sodium Bis(2-methoxyethoxy)aluminum Hydride

Sodium Bis(2-methoxyethoxy)aluminum Hydride

http://www.wikidata.org/entity/Q30049241

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Sodium Bis(2-methoxyethoxy)aluminum Hydride

http://www.wikidata.org/entity/Q30049241

description

2007 nî lūn-bûn

@nan

2007 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի մարտին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@ast

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@en

type

label

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@ast

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@en

prefLabel

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@ast

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@en

P1433

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P1476

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P2860

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P31

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P921

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P356

9780470842898.RS049.PUB2

P1433

Encyclopedia of Reagents for Organic Synthesis

P1476

Sodium Bis(2-methoxyethoxy)aluminum Hydride

@en

P2093

Luiz F. Silva

http://www.w3.org/2001/XMLSchema#string

Melinda Gugelchuk

http://www.w3.org/2001/XMLSchema#string

Ramon S. Vasconcelos

http://www.w3.org/2001/XMLSchema#string

Samir A. P. Quintiliano

http://www.w3.org/2001/XMLSchema#string

P2860

Fluorinated retinoic acids and their analogues. 1. Synthesis and Biological activity of (4-methoxy-2,3,6-trimethylphenyl)nonatetraenoic acid analogues

First total synthesis of taxol. 1. Functionalization of the B ring

Total syntheses of (+)-australine and (-)-7-epialexine.

Total synthesis of (-)- and ent-(+)-vindoline.

Aminoglycoside antibiotics. 2. N,N-Dialkylkanamycins.

On the susceptibility of organic peroxy bonds to hydride reduction.

Novel steroidal inhibitors of human cytochrome P45017 alpha (17 alpha-hydroxylase-C17,20-lyase): potential agents for the treatment of prostatic cancer.

Synthetic studies on (2R,4'R,8'R)-alpha-tocopherol. Facile syntheses of optically active, saturated, acyclic isoprenoids via stereospecific [3,3]sigmatropic rearrangements.

A new one-step strategy for the stereochemical assignment of acyclic 2- and 3-sulfanyl-1-alkanols using the CD exciton chirality method.

Enantioselective synthesis of (-)-terpestacin and (-)-fusaproliferin: clarification of optical rotational measurements and absolute configurational assignments establishes a homochiral structural series.

P31

scholarly article

P356

10.1002/9780470842898.RS049.PUB2

http://www.w3.org/2001/XMLSchema#string

P577

2007-03-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P921