Is Donor−Acceptor Hydrogen Bonding Necessary for 4,6-O-Benzylidene-directed β-Mannopyranosylation? Stereoselective Synthesis of β-C-Mannopyranosides and α-C-Glucopyranosides

David Crich; Indrajeet Sharma

doi:10.1021/ol8017038

Is Donor−Acceptor Hydrogen Bonding Necessary for 4,6-O-Benzylidene-directed β-Mannopyranosylation? Stereoselective Synthesis of β-C-Mannopyranosides and α-C-Glucopyranosides

Organic Letters ◽

10.1021/ol8017038 ◽

2008 ◽

Vol 10 (21) ◽

pp. 4731-4734 ◽

Cited By ~ 32

Author(s):

David Crich ◽

Indrajeet Sharma

Keyword(s):

Hydrogen Bonding ◽

Stereoselective Synthesis ◽

Donor Acceptor

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ChemInform Abstract: Is Donor-Acceptor Hydrogen Bonding Necessary for 4,6-O-Benzylidene-Directed β-Mannopyranosylation? Stereoselective Synthesis of β-C-Mannopyranosides and α-C-Glucopyranosides.

ChemInform ◽

10.1002/chin.200912193 ◽

2009 ◽

Vol 40 (12) ◽

Author(s):

David Crich ◽

Indrajeet Sharma

Keyword(s):

Hydrogen Bonding ◽

Stereoselective Synthesis ◽

Donor Acceptor

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Programed self-assembly of microstructures: self-sorting based on size-matched disk-like molecules and remarkable cooperative reinforcement of hydrogen-bonding and donor–acceptor interaction

Tetrahedron Letters ◽

10.1016/j.tetlet.2011.05.082 ◽

2011 ◽

Vol 52 (29) ◽

pp. 3836-3839 ◽

Cited By ~ 7

Author(s):

Ze-Yun Xiao ◽

Lu Wang ◽

Xin Zhao ◽

Xi-Kui Jiang ◽

Zhan-Ting Li

Keyword(s):

Hydrogen Bonding ◽

Self Assembly ◽

Acceptor Interaction ◽

Donor Acceptor

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Bonding in the trihalides (X3−), mixed trihalides (X2Y−) and hydrogen bihalides (X2H−). The connection between hypervalent, electron-rich three-center, donor–acceptor and strong hydrogen bonding ‡

Journal of the Chemical Society Dalton Transactions ◽

10.1039/a703736h ◽

1997 ◽

pp. 3605-3613 ◽

Cited By ~ 145

Author(s):

Gregory A. Landrum ◽

Norman Goldberg ◽

Roald Hoffmann

Keyword(s):

Hydrogen Bonding ◽

Donor Acceptor

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Synthesis of Complementary Hydrogen Bonding Cyclotriveratrylenes

Journal of Chemical Research ◽

10.3184/030823402103172482 ◽

2002 ◽

Vol 2002 (8) ◽

pp. 359-360 ◽

Cited By ~ 1

Author(s):

Magali Darzac ◽

Stéphanie Montésinos ◽

André Collet ◽

Jean-Pierre Dutasta

Keyword(s):

Hydrogen Bonding ◽

Cyanuric Acid ◽

Donor Acceptor

Two new cyclotriveratrylenes CTV-1 and CTV-2 bearing complementary H-bond donor-acceptor substituents were prepared from 4-hydroxy-3-methoxybenzyl alcohol following a multistep strategy to introduce melamine or cyanuric acid substituents.

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Detection of hydrogen bonding in solution: A 2H nuclear magnetic resonance method based on rotational motion of a donor/acceptor complex

Physical Chemistry Chemical Physics ◽

10.1039/b608147a ◽

2006 ◽

Vol 8 (34) ◽

pp. 4002 ◽

Cited By ~ 3

Author(s):

Nathaniel K. Szymczak ◽

Alan B. Oelkers ◽

David R. Tyler

Keyword(s):

Nuclear Magnetic Resonance ◽

Hydrogen Bonding ◽

Magnetic Resonance ◽

Rotational Motion ◽

Resonance Method ◽

Nuclear Magnetic Resonance Method ◽

Acceptor Complex ◽

Magnetic Resonance Method ◽

Donor Acceptor ◽

Nuclear Magnetic

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Donor–acceptor preassociation, excited state solvation threshold, and optical energy cost as challenges in chemical applications of photobases

Faraday Discussions ◽

10.1039/c8fd00215k ◽

2019 ◽

Vol 216 ◽

pp. 252-268 ◽

Cited By ~ 8

Author(s):

Jonathan Ryan Hunt ◽

Cindy Tseng ◽

Jahan M. Dawlaty

Keyword(s):

Hydrogen Bonding ◽

Excited State ◽

Photon Energy ◽

Energy Cost ◽

Light Energy ◽

Optical Energy ◽

Donor Acceptor

Photobases convert light energy to proton removal power. What limits their applicability? Hydrogen bonding, solvation, and photon energy cost.

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Liquid crystalline G phase of self assembled donor–acceptor molecules by intermolecular hydrogen bonding

Journal of Non-Crystalline Solids ◽

10.1016/j.jnoncrysol.2010.12.076 ◽

2011 ◽

Vol 357 (7) ◽

pp. 1745-1749 ◽

Cited By ~ 1

Author(s):

S. Salma Begum ◽

T. Vindhya Kumari ◽

C. Ravi Shankar Kumar ◽

S. Sreehari Sastry

Keyword(s):

Hydrogen Bonding ◽

Liquid Crystalline ◽

Intermolecular Hydrogen Bonding ◽

Donor Acceptor ◽

Self Assembled ◽

Acceptor Molecules

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Expanding the Genetic Alphabet: Pyrazine Nucleosides That Support a DonorDonorAcceptor Hydrogen-Bonding Pattern

Helvetica Chimica Acta ◽

10.1002/hlca.200490120 ◽

2004 ◽

Vol 87 (6) ◽

pp. 1299-1324 ◽

Cited By ~ 11

Author(s):

Ulrike von Krosigk ◽

Steven A. Benner

Keyword(s):

Hydrogen Bonding ◽

Hydrogen Bonding Pattern ◽

Donor Acceptor ◽

Genetic Alphabet

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Ytterbium Triflate Catalyzed Synthesis of Alkoxy-Substituted Donor−Acceptor Cyclobutanes and Their Formal [4 + 2] Cycloaddition with Imines: Stereoselective Synthesis of Piperidines

Organic Letters ◽

10.1021/ol102062t ◽

2010 ◽

Vol 12 (21) ◽

pp. 4732-4735 ◽

Cited By ~ 72

Author(s):

Mahmoud M. Abd Rabo Moustafa ◽

Brian L. Pagenkopf

Keyword(s):

Stereoselective Synthesis ◽

Ytterbium Triflate ◽

Donor Acceptor

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ChemInform Abstract: REGIOSPECIFIC CHLORINATION OF AROMATIC SUBSTRATES USING DONOR-ACCEPTOR AND HYDROGEN BONDING INTERACTIONS

Chemischer Informationsdienst ◽

10.1002/chin.198020112 ◽

1980 ◽

Vol 11 (20) ◽

Author(s):

A. GUY ◽

M. LEMAIRE ◽

J.-P. GUETTE

Keyword(s):

Hydrogen Bonding ◽

Aromatic Substrates ◽

Hydrogen Bonding Interactions ◽

Donor Acceptor

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