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A practical conversion of an azetidinone to penem : synthesis of Sch 34343

Author
GALA, D; CHIU, J. S; GANGULY, A. K; GIRIJAVALLABHAN, V. M; JARET, R. S; JENKINS, J. K; MCCOMBIE, S. W; NYCE, P. L; ROSENHOUSE, S; STEINMAN, M
Schering Plough res., Bloomfield NJ 07003, United States
Source

Tetrahedron (Oxford. Print). 1992, Vol 48, Num 7, pp 1175-1182 ; ref : 21 ref

CODEN
TETRAB
ISSN
0040-4020
Scientific domain
Organic chemistry
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Acide carboxylique Carbamate organique Composé bicyclique Conversion chimique Hydroxyacide Hétérocycle soufre azote Lactame Sulfure organique 2-Pénème-3-carboxylique acide(2-[(carbamoyloxy) éthylthio]-6-[1-hydroxyéthyl])
Keyword (en)
Carboxylic acid Organic carbamate Bicyclic compound Chemical conversion Hydroxyacid Sulfur nitrogen heterocycle Lactam Organic sulfide
Keyword (es)
Acido carboxílico Carbamato orgánico Compuesto bicíclico Conversión química Hidroxiácido Heterociclo azufre nitrógeno Lactamo Sulfuro orgánico
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06D Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
5191412

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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