PUBLICACIÓN

Enols as feasible acid components in the Ugi condensation

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Castellano T.G., Neo A.G., Marcaccini S., Marcos C.F.

2012 ORGANIC LETTERS

Biochemistry (Q1), Organic Chemistry (Q1), Physical and Theoretical Chemistry (Q1)

JCR: 6.142

SJR: 3.338

CITAS

36

DOI

10.1021/ol302976g

EID

2-s2.0-84871604115

ISSN

1523-7060

EISSN

1523-7052

BIBTEX

@article { fernndezmarcos2012, title = {Enols as feasible acid components in the Ugi condensation}, journal = {Organic Letters}, year = {2012}, volume = {14}, number = {24}, pages = {6218-6221}, author = {Castellano, T.G. and Neo, A.G. and Marcaccini, S. and Marcos, C.F.} }

AUTORES DE LA UEX

Carlos María Fernández Marcos
Ana María Gómez Neo

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New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
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