Results 71 to 80 of about 5,076 (258)

Late‐Stage Functionalization of Peptides on the Solid Phase

open access: yesAngewandte Chemie International Edition, EarlyView.
Peptide modifications are essential to control pharmacodynamic and pharmacokinetic properties of peptide drugs. Consequently, strategies that allow for efficient and rapid incorporation of non‐canonical modifications into peptides in parallel formats are highly sought after.
Marius Werner   +2 more
wiley   +1 more source

2-(4-Chlorophenyl)acetamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2011
In the title compound, C(8)H(8)ClNO, the acetamide group is twisted out the benzene plane with a dihedral angle of 83.08 (1)°. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, forming layers parallel to the ab plane.
Dong-Sheng Ma   +3 more
openaire   +3 more sources

CuBr-mediated radical cascade difluoroacetamidation of acrylamides using α,α-difluoro-α-(TMS)-acetamides

open access: yes, 2017
Radical cascade difluoroacetamidation ofN-(arylsulfonyl)acrylamides with α,α-difluoro-α-(TMS)-acetamides has been achieved for the first time.
Deng-Yuan Li   +4 more
core   +1 more source

Stereodivergent Allylation of Azaaryl Acetamides and Acetates by Synergistic Iridium and Copper Catalysis [PDF]

open access: yes, 2018
We report stereodivergent allylic substitution reactions of allylic esters with prochiral enolates derived from azaaryl acetamides and acetates to form products from addition of the enolates at the most substituted carbon of an allyl moiety with two ...
John F. Hartwig   +5 more
core   +1 more source

Approach for the synthesis of N-phenylamides from β-ketobutylanilides using dimethylformamide and dimethylacetamide as the acyl donors

open access: yesJournal of Saudi Chemical Society, 2015
A new method including the sequence of a CN bond formation of β-keto amides with N,N-dimethylamides and subsequently another two CN bonds cleavage has been developed in the presence of hydrochloric acid.
Cui Chen, Liquan Tan, Peng Zhou
doaj   +1 more source

N-(3-Chlorophenyl)acetamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
The conformation of the N-H bond in the structure of the title compound (3CPA), C(8)H(8)ClNO, is anti to the meta-chloro substituent, in contrast to the syn conformation observed for the ortho-chloro substituent in N-(2-chloro-phen-yl)acetamide, syn to both the ortho and meta chloro substituents in N-(2,3-dichloro-phen-yl)acetamide, and syn to the ...
Hartmut Fuess   +2 more
openaire   +3 more sources

O‑Glycosylation Enabled by N-(Glycosyloxy)acetamides

open access: yes, 2018
A novel glycosylation protocol has been established by using N-(glycosyloxy)­acetamides as glycosyl donors. The N-oxyacetamide leaving group in donors could be rapidly activated in the presence of Cu­(OTf)2 or SnCl4 under microwave irradiation.
Miao Liu (4126252)   +3 more
core   +1 more source

Advanced Separation Technologies for Light Olefin and Alkane (C2‐C4): Recent Advances in Extraction, Adsorption, and Membrane Separation

open access: yesAsia-Pacific Journal of Chemical Engineering, EarlyView.
ABSTRACT With the rapid development of the petrochemical industry, efficient separation technology for olefins and alkanes with the same number of carbon atoms has become an important research topic to enhance the efficiency of petroleum resource utilization and optimize product quality.
Shasha Zhao, Kang Zhao, Zhen Liu
wiley   +1 more source

N-(2,3-Dimethylphenyl)acetamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2009
The conformation of the N-H bond in the structure of the title compound, C(10)H(13)NO, is syn to both the 2- and 3-methyl substituents on the aromatic ring, and is anti to the C=O bond. N-H⋯O hydrogen bonds link the mol-ecules into supra-molecular chains.
Hartmut Fuess   +3 more
openaire   +3 more sources

‐[2‐(Phenylsulfinyl)phenyl]acetamides: A Ring Opening Rearrangement Functionalization (RORF)

open access: yes, 2018
A new telescopic synthesis of N-[2-(phenylthio)phenyl]acetamides has been established using benzo[d]thiazol-2-amine, aryliodide and carboxylic acid via a copper catalyzed ring opening rearrangement functionalization (RORF).
Ahalya Behera   +7 more
core   +1 more source

Home - About - Disclaimer - Privacy