Zobrazeno 1 - 10
of 18
pro vyhledávání: '"V. K. Gumaste"'
Publikováno v:
Synlett. :979-982
A simple and efficient one-pot method for the preparation of allyl azides from allyl alcohols using triphosgene and sodium azide is described. An application of cinnamyl azide for the synthesis of various Nl-cinnamyl azetidin-2-ones is also described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84fff9eaf2ce947f1edf58f28c418587
https://doi.org/10.1055/s-2004-820046
https://doi.org/10.1055/s-2004-820046
Autor:
V. K. Gumaste, Abdul Rakeeb A. S. Deshmukh, D. Krishnaswamy, B. M. Bhawal, Vidyesh V. Govande
Publikováno v:
Tetrahedron. 58:2215-2225
An efficient use of triphosgene, as an acid activator, for the synthesis of substituted azetidin-2-ones via ketene–imine cycloaddition reaction using various acids and imines have been described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::186b7979bf523bbbbac7879f30faacf0
https://doi.org/10.1016/s0040-4020(02)00094-7
https://doi.org/10.1016/s0040-4020(02)00094-7
Publikováno v:
Synlett. 2002:1455-1458
Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune - 411 008, IndiaFax +91(20)5893153; E-mail: arasd@dalton.ncl.res.inReceived 30 May 2002Synlett 2002, No. 9, Print: 02 09 2002. Art Id.1437-2096,E;2002,0,09,1455,1458,ftx,en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de58326c360518302781671ce396bd32
https://doi.org/10.1055/s-2002-33512
https://doi.org/10.1055/s-2002-33512
Publikováno v:
Catalysis Letters. 64:247-250
Linear alkyl benzenes (LAB) are important intermediates in the manufacture of detergents and surface active agents. The alkylation of benzene with linear alcohols using Y‐type zeolite catalysts is described here. The alkylation of benzene with 1‐
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d268da2c8e2ba067e7427bff60c9c3b
https://doi.org/10.1023/a:1019055507996
https://doi.org/10.1023/a:1019055507996
Publikováno v:
Organic Preparations and Procedures International. 31:315-319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ddc7dad9a7496ef3491340f131df33c
https://doi.org/10.1080/00304949909458325
https://doi.org/10.1080/00304949909458325
Publikováno v:
Synthetic Communications. 25:3939-3944
The reaction of various alcohols with paraformaldehyde in presence of montmorillonite to give dialkoxymethanes (2a-g) in very good yield is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::030ac05fe3082e49fe198c5697ed297d
https://doi.org/10.1080/00397919508011470
https://doi.org/10.1080/00397919508011470
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d68485c6092e1606f85d6c728d7cd3b9
https://doi.org/10.1002/chin.199703119
https://doi.org/10.1002/chin.199703119
Publikováno v:
ChemInform. 27
The reaction of various alcohols with paraformaldehyde in presence of montmorillonite to give dialkoxymethanes (2a-g) in very good yield is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b83fe249572a1061a37420fe78adb4ef
https://doi.org/10.1002/chin.199616099
https://doi.org/10.1002/chin.199616099
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb17352cd8ec4f9accde3e9556292a2d
https://doi.org/10.1002/chin.199740088
https://doi.org/10.1002/chin.199740088
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d20088bef9fac0ac3e86064dc35a06e
https://doi.org/10.1002/chin.199942065
https://doi.org/10.1002/chin.199942065