Facile ring opening reaction of oxazolone enables efficient amidation for aminoisobutyric acid
활용도 Analysis
논문 Analysis
연구자 Analysis
저자
조민미
원선우
이동국
윤정연
김선홍
곽영신
제어번호
106053015
학술지명
Archives of Pharmacal Research
권호사항
Vol.
41
No.
5
[
2018
]
발행처
대한약학회
발행처 URL
http://www.psk.or.kr
자료유형
학술저널
수록면
481-489
(
9쪽)
언어
English
출판년도
2018
등재정보
KCI등재
소장기관
부산대학교 중앙도서관
숙명여자대학교 중앙도서관
영남대학교 중앙도서관
영남대학교 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
판매처
'
Facile ring opening reaction of oxazolone enables efficient amidation for aminoisobutyric acid' 의 참고문헌
Thorpe-Ingold effects in cyclizations to five-membered and six-membered rings containing planar segments. The rearrangement of N (1)-alkyl-substituted dihydroorotic acids to hydantoinacetic acids in base
The world of peptides: a brief history of peptide chemistry
The current state of peptide drug discovery: back to the future?
Synthesis of diazoketones derived from <TEX>${\alpha}$</TEX>-amino acids; problem of side reactions
Substituted tyrosyl alanine dipeptide amides. US 4599325
Structural basis for inhibiting <TEX>${\beta}$</TEX>-amyloid oligomerization by a non-coded <TEX>${\beta}$</TEX>-breaker-substituted endomorphin analogue
Neue substituierte Glycinamide, deren Herstellung und deren Berwendung als Arzneimittel. PCT WO 2007/003536 A1
Hepatitis C virus inhibitors cross-referenece to related applications. PCT WO 2015200305
Handbook of biologically active peptides, 2nd edn
Exploiting an inherent neighboring group effect of <TEX>${\alpha}$</TEX>-amino acids to synthesize extremely hindered dipeptides
Discovery of diamide compounds as diacylglycerol acyltransferase 1 (DGAT1) inhibitors
Chemical synthesis of natural product peptides: coupling methods for the incorporation of noncoded amino acids into peptides
Asymmetric inverseelectron- demand hetero-Diels-Alder reaction of six-membered cyclic ketones: an enamine/metal Lewis acid bifunctional approach
An efficient synthetic protocol for amide derivatives of Boc-2- aminoisobutyrate
A neutralization-reionization Mass spectrometric and computational study of oxazolone radicals
3,5,5-trisubstituted hydantoins from activated (Benzyloxycarbonylamino) malonic acids
'
Facile ring opening reaction of oxazolone enables efficient amidation for aminoisobutyric acid'
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