Alternating Copolymers by the Michael-Type Polyaddition Reaction
نویسندگان
چکیده
منابع مشابه
Duplex strand formation using alternating copolymers.
The regular arrangement of complementary diaminopyridine-thymine (DAP-THY) on alternating copolymers permits cooperative binding events and the effective formation of well-controlled micrometre-scale aggregates.
متن کاملmodeling loss data by phase-type distribution
بیمه گران همیشه بابت خسارات بیمه نامه های تحت پوشش خود نگران بوده و روش هایی را جستجو می کنند که بتوانند داده های خسارات گذشته را با هدف اتخاذ یک تصمیم بهینه مدل بندی نمایند. در این پژوهش توزیع های فیزتایپ در مدل بندی داده های خسارات معرفی شده که شامل استنباط آماری مربوطه و استفاده از الگوریتم em در برآورد پارامترهای توزیع است. در پایان امکان استفاده از این توزیع در مدل بندی داده های گروه بندی ...
Chemoresponsive alternating supramolecular copolymers created from heterocomplementary calix[4]pyrroles.
The importance of noncovalent interactions in the realm of biological materials continues to inspire efforts to create artificial supramolecular polymeric architectures. These types of self-assembled materials hold great promise as environmentally stimuli-responsive materials because they are capable of adjusting their various structural parameters, such as chain length, architecture, conformat...
متن کاملConformational Analysis of Alternating Copolymers and Their Association into Nanoarchitectures
Our research focuses on the characterization of the association and the properties in aqueous solution of nanostructures, particularly on nanotubes composed of amphiphilic alternating copolymers. These copolymers constitute a pH sensitive hydrophilic group (maleic anhydride) alternating with a hydrophobic group. To investigate the role of the nature of the hydrophobic groups on the association,...
متن کاملSquaramide-catalysed asymmetric cascade aza-Michael/Michael addition reaction for the synthesis of chiral trisubstituted pyrrolidines.
A bifunctional squaramide catalysed aza-Michael/Michael cascade reaction between nitroalkenes and tosylaminomethyl enones or enoates has been developed. This organocatalytic cascade reaction provides easy access to highly functionalized chiral pyrrolidines with a broad substrate scope, giving the desired products in good yields (up to 99%) with good diastereoselectivities (up to 91 : 9 dr) and ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Kobunshi Kagaku
سال: 1969
ISSN: 1884-8079,0023-2556
DOI: 10.1295/koron1944.26.271