Transition metal-catalyzed enantioselective ring-opening reactions of oxabicyclic alkenes
M Lautens, K Fagnou, S Hiebert - Accounts of chemical research, 2003 - ACS Publications
Over the past five years, several metal-catalyzed asymmetric ring-cleaving reactions have
been developed that generate ring-opened products in high yield and enantiomeric excess …
been developed that generate ring-opened products in high yield and enantiomeric excess …
Synthesis and conformational and biological aspects of carbasugars
Carbohydrate chemistry constitutes today a “multifaceted” discipline strongly connected with
organic, pharmaceutical, and medicinal chemistry. 1 Carbohydrates are important …
organic, pharmaceutical, and medicinal chemistry. 1 Carbohydrates are important …
[BUCH][B] The organic chemistry of sugars
DE Levy, P Fügedi - 2005 - taylorfrancis.com
Intrigued as much by its complex nature as by its outsider status in traditional organic
chemistry, the editors of The Organic Chemistry of Sugars compile a groundbreaking …
chemistry, the editors of The Organic Chemistry of Sugars compile a groundbreaking …
Modern methods of monosaccharide synthesis from non-carbohydrate sources
T Hudlicky, DA Entwistle, KK Pitzer, AJ Thorpe - Chemical reviews, 1996 - ACS Publications
Humans have utilized carbohydrates in natural forms such as cellulose in cotton, sucrose in
cane sugar, and sucrose, D-fructose, and D-glucose in honey from the dawn of civilization …
cane sugar, and sucrose, D-fructose, and D-glucose in honey from the dawn of civilization …
Using ring-opening reactions of oxabicyclic compounds as a strategy in organic synthesis
This chapter discusses the various methods for the preparation of oxabicyclic compounds,
with an emphasis on the stereo-and enantioselective synthesis of these substances …
with an emphasis on the stereo-and enantioselective synthesis of these substances …
Synthesis of l-Hexoses
In this review we focus on the synthesis of compounds that are the rare antipodes of
common hexoses. Therefore, we only cover L-aldohexoses, 2-keto-L-hexoses, and 6-deoxy …
common hexoses. Therefore, we only cover L-aldohexoses, 2-keto-L-hexoses, and 6-deoxy …
Diels− Alder reaction of 2-amino-substituted furans as a method for preparing substituted Anilines
A Padwa, M Dimitroff, AG Waterson… - The Journal of Organic …, 1997 - ACS Publications
5-Amino-2-furancarboxylic acid methyl ester undergoes a facile Diels− Alder cycloaddition
with a variety of dienophiles to afford ring-opened cycloadducts that are readily dehydrated …
with a variety of dienophiles to afford ring-opened cycloadducts that are readily dehydrated …
Several convenient methods for the synthesis of 2-amido substituted furans
A Padwa, KR Crawford… - The Journal of Organic …, 2003 - ACS Publications
Several new methods for the synthesis of differently substituted 2-amidofurans are
described. The thermolysis of furan-2-carbonyl azide results in a Curtius rearrangement and …
described. The thermolysis of furan-2-carbonyl azide results in a Curtius rearrangement and …
Nickel-catalyzed highly stereoselective ring opening of 7-oxa-and azanorbornenes with organic halides
CC Feng, M Nandi, T Sambaiah… - The Journal of Organic …, 1999 - ACS Publications
Nickel-catalyzed ring-opening reactions of 7-heteroatom norbornadienes and norbornenes
with various organic halides to give products with multiple stereocenters are described …
with various organic halides to give products with multiple stereocenters are described …
Formal total synthesis of (±)-γ-lycorane and (±)-1-deoxylycorine using the [4+ 2]-cycloaddition/rearrangement cascade of furanyl carbamates
A Padwa, MA Brodney, SM Lynch - The Journal of Organic …, 2001 - ACS Publications
The total syntheses of γ-lycorane and (±)-1-deoxylycorine were accomplished using an
intramolecular Diels− Alder cycloaddition of a furanyl carbamate as the key step. The initially …
intramolecular Diels− Alder cycloaddition of a furanyl carbamate as the key step. The initially …