Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Z. A. Stumbrevichute"'
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 20:2140-2143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b0a26a455af2c9ea54d91b11bd3d25a
https://doi.org/10.1007/bf00851266
https://doi.org/10.1007/bf00851266
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 21:1530-1534
1. Benzenesulfenyl chloride adds to dimethylacrylic acid and its derivatives with the formation of mixtures of adducts ofα-chloro-β-phenylthio- andβ-chloro-α-phenylthioisovaleric acids and their derivatives, respectively. 2. α-Chloro-β-phenylth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e4fc6f0b36a5c074053ab36969bc9f
https://doi.org/10.1007/bf00850510
https://doi.org/10.1007/bf00850510
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 17:1775-1777
The authors have shown by NMR spectroscopy that addition of methyl- and phenylsulfenylchloride to methacrylic acid and its anilide leads to formation ofα-methyl- andα-phenylthio-β-chloro derivatives of propionic acid, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e665356cce191e6ddf4962e47a9c8cb
https://doi.org/10.1007/bf01169895
https://doi.org/10.1007/bf01169895
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07506cc36dce3888cb5dec04078b4190
https://doi.org/10.1002/chin.197150270
https://doi.org/10.1002/chin.197150270
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eef17ff98c6e956cdbdcef96e203a36
https://doi.org/10.1002/chin.197206193
https://doi.org/10.1002/chin.197206193
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::112cebddf969ea8158219f9a2cac71b2
https://doi.org/10.1002/chin.197123226
https://doi.org/10.1002/chin.197123226
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::251687f88a2a317f324f24d8ad095ae2
https://doi.org/10.1002/chin.197220343
https://doi.org/10.1002/chin.197220343
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 18:1920-1921
α-Chloro-β-alkylthiobutyric acid derivatives are formed preferentially initially on addingβ-chloroethylsulfenyl chloride to crotonic acid, its acid chloride, ethyl ester, amide, and anilide; these adducts are relatively rapidly isomerized toα-alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::580bb0a143088af0bf8f9dc9ccda705e
https://doi.org/10.1007/bf00905846
https://doi.org/10.1007/bf00905846
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 20:1714-1715
Alkylsulfenyl chlorides react with cinnamic acid and its derivatives to yield only one stable adduct, namely theα-alkylthio-β-chloro-β-phenylpropionic acid and its derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0af8899a37b9fa13ce458cb5a4924f2e
https://doi.org/10.1007/bf00860041
https://doi.org/10.1007/bf00860041
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 21:215-215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9307d12d5b1d796a13608371e0c037c1
https://doi.org/10.1007/bf00855706
https://doi.org/10.1007/bf00855706