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Amino 그룹 보호
아미노는 추가 반응을 위해 그대로 유지되어야 하므로 이를 보호해야 합니다.이것은 보통 Boc(숙정산소졸기)와 같은 보호기단을 도입함으로써 이루어진다.
화학 원료를 구입해야하는 경우 요청 정보를 제출하여최신견적을받으십시오.
Amino 그룹 보호의 학술 논문
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The efficient synthesis of a bis-glycosylated steroid drug transport reagent: Methyl 3-β-amino-7α, 12α-di(1' α-glucosyl)-5β-cholate (TC002)
화학 물질
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phenyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside sulfoxide
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PhSH
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One-pot synthesis of orthogonally protected enantiopure S-(aminoalkyl)-cysteine derivatives
화학 물질
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L-Cysteine, S-[(2S)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-3-phenylpropyl]-, ethyl ester
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Hydantoin derivatives of L- and D-amino acids: Synthesis and evaluation of their antiviral and antitumoral activity
화학 물질
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N-(1-benzotriazolecarbonyl)-L-leucine diphenylmethylamide
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Synthesis of acyclic nucleotide analogues derived from 2-amino-6-C-substituted purines via cross-coupling reactions of 2-amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl}-6-halopurines with diverse organometallic reagents
화학 물질
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2-Amino-9-{2-[(diisopropoxyphosphoryl)methoxy]ethyl}-6-phenylpurine
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Stereoselective synthesis of [2S,3R]-β-hydroxy ornithine
화학 물질
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2H-Pyran, tetrahydro-2-[[5-[(4-methoxyphenyl)methoxy]-2-pentenyl]oxy]-, (Z)-
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