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isoretronecanol

 
National Institutes of Health

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2015
2015
The cyano group was used as a traceless activation group for the [3+2] cycloaddition of azomethine ylides in a two-step process… Expand
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2015
2015
INTRODUCTION The freshwater aquatic plant Gymnocoronis spilanthoides (Senegal tea plant, jazmín del bañado, Falscher Wasserfreund… Expand
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2014
2014
CONSPECTUS: Lactones and lactams are a well-known class of natural products and can be used as building blocks in organic… Expand
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2006
2006
Phalaenopsis hybrids contain two 1,2-saturated pyrrolizidine monoesters, T-phalaenopsine (necine base trachelanthamidine) and its… Expand
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2006
2006
An efficient photoinduced radical addition of tertiary amine, mainly cyclic derivatives, to electron-deficient alkenes was… Expand
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2004
2004
By means of thin layer chromatography pyrrolizidine alkaloids and phenolic compounds in some members of the familyBoraginaceae… Expand
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2000
2000
The photochemical reactivites of 1-aza and 2-azabicyclo[2.2.2]oct-2-en-5-ones have been studied. There is a strong correlation… Expand
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1999
1999
A new method for the stereocontrolled synthesis of pyrrolizidine and indolizidine alkaloids by means of titanium-mediated… Expand
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1986
1986
(+/-)-[3,5-14C]Trachelanthamidine and (+/-)-[5-3H]isoretronecanol, which are diastereomers, were prepared from potassium [14C… Expand
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1971
1971
Abstract The pyrrolizidine aminoalcohols supinidine, hydroxyheliotridane, isoretronecanol, heliotridine, retronecine… Expand
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