Zobrazeno 1 - 8
of 8
pro vyhledávání: '"John Eugene Nidhiry"'
Publikováno v:
Synlett. 25:2585-2590
A facile general route for the synthesis of azepino[4,5-b]indolones is presented. The strategy involves a Bronsted acid assisted intramolecular cyclization of unsaturated tryptamides. The methodology developed has been applied to the synthesis of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30a8a61d73d1907999aa71b043da1542
https://doi.org/10.1055/s-0034-1379083
https://doi.org/10.1055/s-0034-1379083
Publikováno v:
Tetrahedron. 70:4611-4616
The total synthesis of new indole alkaloids henrycinol A and B were accomplished starting from l -tryptophan methyl ester. The key step is a stereochemically flexible Pictet–Spengler reaction governed by the presence or absence of an N-allyl group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9718389c3482f6e6c8a2d09925d641c1
https://doi.org/10.1016/j.tet.2014.05.028
https://doi.org/10.1016/j.tet.2014.05.028
Publikováno v:
Tetrahedron. 69:5525-5536
An enantiospecific total synthesis of indole alkaloids eburnamonine, aspidospermidine and quebrachamine is described from lactic acid. Synthesis of all three alkaloids is accomplished from a single chiral building block. Johnson–Claisen rearrangeme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29445ca6c3da2b5f1dec21e581fb1a60
https://doi.org/10.1016/j.tet.2013.04.097
https://doi.org/10.1016/j.tet.2013.04.097
Publikováno v:
Synlett. 23:1477-1480
The enantiospecific total synthesis of vinca alkaloid (+)-eburnamonine is accomplished from l -ethyl lactate. Key feature of the synthesis is the construction of the chiral quaternary center involving a Johnson–Claisen rearrangement and assembly of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c572544963ce7a97baf91bb584f7c9e
https://doi.org/10.1055/s-0031-1291143
https://doi.org/10.1055/s-0031-1291143
Publikováno v:
Synthesis. 2010:2521-2526
The enantiodivergent formal syntheses of both enantiomers of aspercyclide C is accomplished. Starting from L-(+)-tartaric acid, the key protected allylic alcohol, (3R,4R)-4-(methoxy-methoxy) non-1-en-3-ol is prepared, and is then elaborated into both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d69e229da7ccf4eb2d6ecad2c71f6f7
https://doi.org/10.1055/s-0029-1218831
https://doi.org/10.1055/s-0029-1218831
Publikováno v:
ChemInform. 46
A facile general route for the synthesis of azepino[4,5-b]indolones is presented. The strategy involves a Bronsted acid assisted intramolecular cyclization of unsaturated tryptamides. The methodology developed has been applied to the synthesis of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d522e72b2834cd430585937697eb6c87
https://doi.org/10.1002/chin.201515244
https://doi.org/10.1002/chin.201515244
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3740b256f4e6bb8049e760234319d3ae
https://doi.org/10.1002/chin.201451206
https://doi.org/10.1002/chin.201451206
Publikováno v:
ChemInform. 41
The enantiodivergent formal syntheses of both enantiomers of aspercyclide C is accomplished. Starting from L-(+)-tartaric acid, the key protected allylic alcohol, (3R,4R)-4-(methoxy-methoxy) non-1-en-3-ol is prepared, and is then elaborated into both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bacf0a069cb3c16c2eba71ca2d715991
https://doi.org/10.1002/chin.201049215
https://doi.org/10.1002/chin.201049215