2026-09-19T14:22:21Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/437732022-01-13T07:54:21Zcom_1721.1_7582com_1721.1_7581col_1721.1_131022
Mohammad Movassaghi.
Schmidt, Michael Anthony, 1980-
Massachusetts Institute of Technology. Dept. of Chemistry.
Massachusetts Institute of Technology. Department of Chemistry
2008-12-11T18:25:24Z
2008-12-11T18:25:24Z
2008
2008
http://hdl.handle.net/1721.1/43773
260457144
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2008.
Vita.
Includes bibliographical references.
I. The Development of a General Strategy Towards Dimeric Hexahydropyrroloindole Alkaloids. A Concise Total Synthesis of (+)-Chimonanthine, (+)-Folicanthine and (-)Calycanthine. An efficient and convergent strategy for the synthesis of dimeric hexahydropyrroloindole alkaloids is described. The simultaneous formation of the vicinal quaternary stereocenters using a reductive dimerization reaction provides gram-scale access to an optically active key intermediate employed in the synthesis of (+)-chimonanthine, (+)-folicanthine, and (-)calycanthine. II. The Development of a General Strategy Towards Dimeric Hexahydropyrroloindole Alkaloids. A Concise Total Synthesis of (+)-WIN 64821, (-)-Ditryptophenaline and (-)-1'(2-Phenylethylene)-ditryptophenaline. The concise enantioselective total synthesis of (+)-WIN 64821 and (-)-ditryptophenaline in six and seven steps, respectively, from commercially available amino acid derivatives is described. The gram-scale synthesis of key intermediates and simultaneous introduction of the vicinal quaternary stereocenters provides a highly effective and preparative synthesis of these natural alkaloids. Additionally, the synthesis and structural confirmation of the natural alkaloid (-)-1 '-(2-phenylethylene)-ditryptophenaline is described. III. N-Heterocyclic Carbene-Alcohol Hydrogen Bonds. Studies and Application in the Amidation of Unactivated Esters. A single-step and catalytic amidation of unactivated esters with amino alcohols is described. Treatment of equimolar quantities of amino alcohols and unactivated esters with N,Nbismestiylimidazolylidene (5 mol%) affords the desired amides in high yield under mild reaction conditions.
(cont.) The compatibility of the present methodology with a wide range of functional groups, heterocycles, and optically active substrates in addition to both aromatic and aliphatic esters is noteworthy. Preliminary data regarding an unprecedented hydrogen-bonded carbene-alcohol complex is reported. Further investigation of this hydrogen bond revealed steric and electronic influences on the nature of this bond, cumulating in discovery of a practical metal free method for the stabilization and storage of these nitrogen heterocyclic carbenes. Also described is a method for the synthesis of optically active imidazo-[1,5-a]-pyridinium salts as precursors to optically active nitrogen heterocyclic carbenes.
by Michael Anthony Schmidt.
Ph.D.
338 p.
eng
Massachusetts Institute of Technology
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http://dspace.mit.edu/handle/1721.1/7582
Chemistry.
The development of new synthetic strategies and methodologies for complex alkaloid total synthesis : a concise synthesis of (+)-chimonanthine, (+)-WIN 64821, (-)-ditryptophenaline and related alkaloids
Concise synthesis of (+)-chimonanthine, (+)-WIN 64821, (-)-ditryptophenaline and related alkaloids
Thesis
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<Abstract>I. The Development of a General Strategy Towards Dimeric Hexahydropyrroloindole Alkaloids. A Concise Total Synthesis of (+)-Chimonanthine, (+)-Folicanthine and (-)Calycanthine. An efficient and convergent strategy for the synthesis of dimeric hexahydropyrroloindole alkaloids is described. The simultaneous formation of the vicinal quaternary stereocenters using a reductive dimerization reaction provides gram-scale access to an optically active key intermediate employed in the synthesis of (+)-chimonanthine, (+)-folicanthine, and (-)calycanthine. II. The Development of a General Strategy Towards Dimeric Hexahydropyrroloindole Alkaloids. A Concise Total Synthesis of (+)-WIN 64821, (-)-Ditryptophenaline and (-)-1'(2-Phenylethylene)-ditryptophenaline. The concise enantioselective total synthesis of (+)-WIN 64821 and (-)-ditryptophenaline in six and seven steps, respectively, from commercially available amino acid derivatives is described. The gram-scale synthesis of key intermediates and simultaneous introduction of the vicinal quaternary stereocenters provides a highly effective and preparative synthesis of these natural alkaloids. Additionally, the synthesis and structural confirmation of the natural alkaloid (-)-1 '-(2-phenylethylene)-ditryptophenaline is described. III. N-Heterocyclic Carbene-Alcohol Hydrogen Bonds. Studies and Application in the Amidation of Unactivated Esters. A single-step and catalytic amidation of unactivated esters with amino alcohols is described. Treatment of equimolar quantities of amino alcohols and unactivated esters with N,Nbismestiylimidazolylidene (5 mol%) affords the desired amides in high yield under mild reaction conditions.</Abstract>
<Abstract>(cont.) The compatibility of the present methodology with a wide range of functional groups, heterocycles, and optically active substrates in addition to both aromatic and aliphatic esters is noteworthy. Preliminary data regarding an unprecedented hydrogen-bonded carbene-alcohol complex is reported. Further investigation of this hydrogen bond revealed steric and electronic influences on the nature of this bond, cumulating in discovery of a practical metal free method for the stabilization and storage of these nitrogen heterocyclic carbenes. Also described is a method for the synthesis of optically active imidazo-[1,5-a]-pyridinium salts as precursors to optically active nitrogen heterocyclic carbenes.</Abstract>
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