- 홈페이지 > 화학 용어 > 보호 및 보호 해제
보호 및 보호 해제
펩타이드 합성 과정에서 반응의 영역 선택성을 조절하는 데 있어서 보호 기단이 필수적입니다.보호기단을 사용하여 반응성 관능단을 마스킹하고 필요할 때 선택적으로 보호를 해제할 수 있습니다.
화학 원료를 구입해야하는 경우 요청 정보를 제출하여최신견적을받으십시오.
보호 및 보호 해제의 학술 논문
-
Synthesis of chiral cyclobutane containing C 3-symmetric peptide dendrimers
화학 물질
-
(S)-tert-butyl 3-((1R,3R)-3-acetyl-2,2-dimethylcyclobutyl)-4-(4-(benzyloxycarbonylamino)butanamido)butanoate
-
-
Synthesis of neothramycins A and B
화학 물질
-
(S)-5-Hydroxymethyl-1-(2-nitro-benzoyl)-pyrrolidin-2-one
-
-
Synthesis of a biologically active triazole-containing analogue of cystatin A through successive peptidomimetic alkyne-azide ligations
화학 물질
-
4-(4-{[(9H-fluoren-9-ylmethoxycarbonyl)prop-2-ynylamino]methyl}-3,5-dimethoxyphenoxy)butyric acid
-
-
Synthesis of (-)-Fumagillin
화학 물질
-
푸마 길롤
-
-
A Baylis-Hillman approach to the synthesis of C1-C11 fragment of caribenolide I
화학 물질
-
2-(1-hydroxy-3-p-methoxybenzyloxypropyl)acrylic acid methyl ester
-
-
SYNTHESIS OF THE OLIGOSACCHARIDE MOIETIES OF MUSETTAMYCIN AND MARCELLOMYCIN, NEW ANTITUMOUR ANTIBIOTICS
화학 물질
-
Acetic acid (2S,3R,4R,5R,6S)-3-acetoxy-6-{(2S,3R,4S,6S)-4-benzyloxy-6-[(2S,3S,4S,6R)-6-benzyloxy-2-methyl-4-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-3-yloxy]-2-methyl-tetrahydro-pyran-3-yloxy}-5-iodo-2-methyl-tetrahydro-pyran-4-yl ester
-
-
An efficient construction of bicyclic systems containing a seven-membered ring by tandem ring-closing metathesis reactions of dienynes
화학 물질
-
Triethyl-((1S,2R,3S,4R)-2,3,4-tris-benzyloxy-1-but-3-enyl-1-ethynyl-hex-5-enyloxy)-silane
-
-
Synthesis of enantiomerically pure (S)-methanocarbaribo uracil nucleoside derivatives for use as antiviral agents and P2Y receptor ligands
화학 물질
-
ethyl (2R,5R)-5-[[(tert-butyldiphenylsilyl)oxy]methyl]-8,8-dimethyl-7,9-dioxatricyclo[4.3.0.02,4]nonane-2-carboxylate
-
-
Total Synthesis of Halicholactone and Neohalicholactone
화학 물질
-
2(3H)-Furanone, dihydro-4-[(4-methoxyphenyl)methoxy]-, (4S)-
-
-
A stereocontrolled total synthesis of (±)-saframycin A
화학 물질
-
(+/-)-Saframycin A
-
-
STEREOCONTROLLED SYNTHESIS OF THE BRASSINOLIDE SIDE CHAIN VIA A PYRANONE DERIVATIVE
화학 물질
-
2α,3α,22α,23α-tetrahydroxy-24β-methyl-B-homo-7-oxa-5α-cholestan-6-one
-
Lithium diisopropylamide
-
메틸 요오드화물
-
-
Synthesis of [13]-membered macrocyclic stevastelins via a transesterification reaction as the key step: Total synthesis of stevastelin C3
화학 물질
-
L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-L-valyl-L-threonyl-O-(phenylmethyl)-, (1R,2S)-1-[(1S)-2-hydroxy-1-methylethyl]-2-methylhexadecyl ester
-
-
Biocatalytic Strategy for Highly Diastereo- and Enantioselective Synthesis of 2,3-Dihydrobenzofuran-Based Tricyclic Scaffolds
화학 물질
-
7-Bromo-5-fluorobenzo[b]furan
-
-
Synthesis of New 1,2,3-Triazolo[1,2-a]benzotriazole Derivatives or Substituted 2,3-Benzo-13a,6,6a-tetraazapentalenes. II
화학 물질
-
1-(2-nitrophenyl)-4-carboethoxy-5-methyl-1H-1,2,3-triazole
-
-
Enantio- and diastereocontrolled synthesis of (-)-19(S)-acetoxy-N1- acetyl-20-epitubifolidine
화학 물질
-
[2-((1R,3aS,4S,7aR)-6-Methoxy-4-methyl-hexahydro-furo[3,4-c]pyran-1-ylethynyl)-phenyl]-carbamic acid ethyl ester
-
-
Chemo-enzymatic synthesis of (2S,4R)-2-amino-4-(3-(2,2-diphenylethylamino)- 3-oxopropyl)pentanedioic acid:
Anovel selective inhibitor of human excitatory amino acid transporter subtype 2화학 물질
-
dimethyl 2-(3-benzylamino-3-oxopropyl)-4-oxoglutarate
-
