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4,589 Newest Publications in organic letters

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Correction to Bright, Color-Tunable Fluorescent Dyes Based on π-Expanded Diketopyrrolopyrroles

02-Jan-2015 | Marek Grzybowski; Eliza Glodkowska-Mrowka; Tomasz Stoklosa; Daniel T. Gryko, Organic Letters, 2015

Organic Letters DOI: 10.1021/ol5035782

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Mild Palladium-Catalyzed Cyanation of (Hetero)aryl Halides and Triflates in Aqueous Media

02-Jan-2015 | Daniel T. Cohen; Stephen L. Buchwald, Organic Letters, 2015

Organic Letters DOI: 10.1021/ol5032359

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Diversity-Oriented Facile Access to Highly Fluorescent Membrane-Permeable Benz[c,d]indole N-Heteroarene BF2 Dyes

31-Dec-2014 | Chi Cheng; Naixun Gao; Changjiang Yu; Zhaoyun Wang; Jun Wang; Erhong Hao; Yun Wei; Xiaolong Mu; Yanli Tian; Chongzha ..., Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503379c

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Chiral Primary Amine Catalyzed Asymmetric Michael Addition of Malononitrile to α-Substituted Vinyl Ketone

31-Dec-2014 | Niankai Fu; Long Zhang; Sanzhong Luo, Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503566a

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2-Halogenoimidazolium Salt Catalyzed Aza-Diels–Alder Reaction through Halogen-Bond Formation

31-Dec-2014 | Youhei Takeda; Daichi Hisakuni; Chun-Hsuan Lin; Satoshi Minakata, Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503426f

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Ruthenium-Catalyzed Reductive Amination without an External Hydrogen Source

31-Dec-2014 | Pavel N. Kolesnikov; Niyaz Z. Yagafarov; Dmitry L. Usanov; Victor I. Maleev; Denis Chusov, Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503595m

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Catalytic Asymmetric Construction of Pyrroloindolines via an in Situ Generated Magnesium Catalyst

31-Dec-2014 | Linqing Wang; Dongxu Yang; Fengxia Han; Dan Li; Depeng Zhao; Rui Wang, Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503455r

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Practical Route to 2-Quinolinones via a Pd-Catalyzed C–H Bond Activation/C–C Bond Formation/Cyclization Cascade Reaction

29-Dec-2014 | Junliang Wu; Shaohua Xiang; Jing Zeng; Minli Leow; Xue-Wei Liu, Organic Letters, 2014

Organic Letters DOI: 10.1021/ol503292p

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Semipermanent C-Terminal Carboxylic Acid Protecting Group: Application to Solubilizing Peptides and Fragment Condensation

29-Dec-2014 | Marta Paradís-Bas; Judit Tulla-Puche; Fernando Albericio, Organic Letters, 2014

The 2-methoxy-4-methylsulfinylbenzyl alcohol (Mmsb-OH) safety-catch linker has been described as a useful tool to overcome two obstacles in peptide synthesis: the solubility and fragment condensation of peptides. The incorporation of the linker into an insoluble peptide target, thereby allowing ...

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