Schwan Adrian L相关文献与解析，生知库 | 链接生命科学的每一步

Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides

碱诱导苄基炔基硫醚5-内环化反应的合成范围、计算化学和机理

期刊:Tetrahedron

影响因子:2.2

doi:10.1016/j.tet.2010.11.104

Motto, John M; Castillo, Alvaro; Greer, Alexander; Montemayer, Laura K; Sheepwash, Erin E; Schwan, Adrian L

发表日期：2011

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Synthesis and activity of a novel diether phosphonoglycerol in phospholipase-resistant synthetic lipid:peptide lung surfactants()

新型二醚膦酸甘油酯在抗磷脂酶合成脂质：肽肺表面活性剂中的合成及活性研究()

期刊:Medchemcomm

影响因子:

doi:10.1039/C1MD00206F

Schwan, Adrian L; Singh, Suneel P; Davy, Jason A; Waring, Alan J; Gordon, Larry M; Walther, Frans J; Wang, Zhengdong; Notter, Robert H

发表日期：2011

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Bis(2-bromo-benz-yl) tris-ulfide

双(2-溴苯甲基)三硫化物

期刊:Acta Crystallographica Section E-Structure Reports Online

影响因子:0.6

doi:10.1107/S1600536809001834

Singh, Suneel P; Lough, Alan J; Schwan, Adrian L

发表日期：2009

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Monoclinic modification of N-[(1,1-dimethyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 200â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯在 200°(1) K 下的单斜晶系改性

期刊:Acta Crystallographica Section E-Structure Reports Online

影响因子:0.6

doi:10.1107/S1600536809019023

Singh Suneel P, Verdu Marcus J, Lough Alan J, Schwan Adrian L

发表日期：2009

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Triclinic modification of N-[(1,1-di-methyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 120â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯的三斜晶系改性在 120°(1) K 下

期刊:Acta Crystallographica Section E-Structure Reports Online

影响因子:0.6

doi:10.1107/S1600536809019011

Singh Suneel P, Verdu Marcus J, Lough Alan J, Schwan Adrian L

发表日期：2009

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Activity and inhibition resistance of a phospholipase-resistant synthetic surfactant in rat lungs

大鼠肺中抗磷脂酶合成表面活性剂的活性和抑制抵抗性

期刊:American Journal of Respiratory Cell and Molecular Biology

影响因子:5.3

doi:10.1165/rcmb.2006-0434OC

Wang, Zhengdong; Chang, Yusuo; Schwan, Adrian L; Notter, Robert H

Rat

发表日期：2007

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The Synthesis and Base-Induced Breakdown of Triaryl 1,4-Oxathiins-An Experimental and DFT Study

三芳基1,4-氧硫杂环己烯的合成及碱诱导分解——实验与DFT研究

Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides

碱诱导苄基炔基硫醚5-内环化反应的合成范围、计算化学和机理

Synthesis and activity of a novel diether phosphonoglycerol in phospholipase-resistant synthetic lipid:peptide lung surfactants()

新型二醚膦酸甘油酯在抗磷脂酶合成脂质：肽肺表面活性剂中的合成及活性研究()

Bis(2-bromo-benz-yl) tris-ulfide

双(2-溴苯甲基)三硫化物

Monoclinic modification of N-[(1,1-dimethyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 200â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯在 200°(1) K 下的单斜晶系改性

Triclinic modification of N-[(1,1-di-methyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 120â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯的三斜晶系改性在 120°(1) K 下

Activity and inhibition resistance of a phospholipase-resistant synthetic surfactant in rat lungs

大鼠肺中抗磷脂酶合成表面活性剂的活性和抑制抵抗性

The Synthesis and Base-Induced Breakdown of Triaryl 1,4-Oxathiins-An Experimental and DFT Study

三芳基1,4-氧硫杂环己烯的合成及碱诱导分解——实验与DFT研究

Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides

碱诱导苄基炔基硫醚5-内环化反应的合成范围、计算化学和机理

Synthesis and activity of a novel diether phosphonoglycerol in phospholipase-resistant synthetic lipid:peptide lung surfactants()

新型二醚膦酸甘油酯在抗磷脂酶合成脂质：肽肺表面活性剂中的合成及活性研究()

Bis(2-bromo-benz-yl) tris-ulfide

双(2-溴苯甲基)三硫化物

Monoclinic modification of N-[(1,1-dimethyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 200â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯在 200°(1) K 下的单斜晶系改性

Triclinic modification of N-[(1,1-di-methyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 120â (1) K.

N-[(1,1-二甲基乙氧基)羰基]-3-[(R)-丙-2-烯-1-基亚磺酰基]-(R)-丙氨酸乙酯的三斜晶系改性在 120°(1) K 下

Activity and inhibition resistance of a phospholipase-resistant synthetic surfactant in rat lungs

大鼠肺中抗磷脂酶合成表面活性剂的活性和抑制抵抗性

Monoclinic modification of N-[(1,1-dimethyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 200â (1) K.

Triclinic modification of N-[(1,1-di-methyl-ethoxy)carbon-yl]-3-[(R)-prop-2-en-1-ylsulfin-yl]-(R)-alanine ethyl ester at 120â (1) K.