Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl alpha-Amino Acids using 4-tert-Butoxycarbonyl-5,6Diphenylmorpholin-2- one: (R)-(N-tert-Butoxycarbonyl) allylglycine (4-Pentenoic acid, 2[[(1,1-Dimethylethoxy)carbonyl]amino]-, (2R)-)

被引：0

作者：

Looper, Ryan E. ^{[1
]}

Williams, Robert M. ^{[2
]}

机构：

[1] Colorado State Univ, Ft Collins, CO 80523 USA

[2] Univ Utah, Salt Lake City, UT 84112 USA

来源：

ORGANIC SYNTHESES | 2012年 / 89卷

关键词：

D O I：

10.15227/orgsyn.089.0394

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：394 / 403

页数：10

共 13 条

[1] Diethyl(2S,3R)-2-(N-tert-butoxycarbonyl)amino-3-hydroxysuccinate
Saito, S
Komada, K
Moriwake, T
ORGANIC SYNTHESIS, VOL 73, 1996, 73 : 184 - 200
[2] Synthesis of the intermediate of gemifloxacin by the chemoselective hydrogenation of 4-cyano-3-methoxyimino-1-(N-tert-butoxycarbonyl)pyrrolidine.: Part 2.: The palladium catalysts in acidic media
Noh, HK
Lee, JS
Kim, Y
Hwang, G
Chang, JH
Shin, H
Nam, DH
Lee, KH
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2004, 8 (05) : 788 - 795
[3] Silylcupration of (R)-2,2-dimethyl-3-(tert-butoxycarbonyl)-4-ethynyloxazolidine:: A stereoselective approach to the synthesis of γ-silylated saturated and unsaturated α-amino acids
Reginato, G
Mordini, A
Valacchi, M
Grandini, E
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (25): : 9211 - 9216
[4] Chiral hydroxylamines .2. (1R,2R)-N-benzyl-N-[(3-tert-butoxycarbonyl-2,2-di-methyloxazol-4-yl) (furan-2-yl)methyl]-hydroxylamine
Merino, P
Merchan, FL
Tejero, T
Lanaspa, A
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1996, 52 : 2536 - 2538
[5] Synthesis of (2R, 4R)-2-N-tert-Butyloxycarbonyl Amino-4,5-epoxido-valeric Acid Methyl Ester
Xin Rong QIN*
Chinese Chemical Letters, 2002, (02) : 111 - 112
[6] Synthesis of (2R, 4R)-2-N-tert-butyloxycarbonyl amino-4,5-epoxido-valeric acid methyl ester
Qin, XR
Xie, YL
Zhang, QL
Luo, HB
Xie, YY
CHINESE CHEMICAL LETTERS, 2002, 13 (02) : 111 - 112
[7] The Concise Synthesis of a tert-Butoxycarbonyl Derivative of (3R,4S)-4-Amino-3-hydroxy-7-(N-nitrosohydroxyamino)-2,2-dimethylheptanoate, a Component of JBIR-141
Yasoshima, Kotaro
Yoshida, Masahito
Doi, Takayuki
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2022, 95 (05) : 830 - 832
[8] Peptide inhibitors of aspartic proteinases with hydroxyethylene isostere replacement of peptide bond. I. Preparation of four diastereoisomeric (2R or 2S,4R or 4S,5S)-2-benzyl-5-[(tert-butoxycarbonyl)amino]-4-hydroxy-6-phenylhexanoic acids
Litera, J
Budesinsky, M
Urban, J
Soucek, M
COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1998, 63 (02) : 231 - 244
[9] Peptide Inhibitors of Aspartic Proteinases with Hydroxyethylene Isostere Replacement of Peptide Bond. I. Preparation of Four Diastereoisomeric (2R or 2S,4R or 4S,5S)2-Benzyl-5-[(tert-Butoxycarbonyl)amino]-4$ MIN@hydroxy-6-phenylhexanoic Acids
Litera, J.
Budesinsky, M.
Urban, J.
Soucek, M.
Collection of Czechoslovak Chemical Communications, 63 (02):
[10] NOVEL ANIONIC REAGENTS FOR THE STEREOSELECTIVE SYNTHESIS OF GAMMA-HYDROXY-ALPHA-AMINO-ACIDS - AN X-RAY CRYSTALLOGRAPHIC STUDY OF 2R(S)-BENZOYLAMINO-N-TERT-BUTYL-4R(S)-HYDROXY-4-(4-METHOXYPHENYL)-3R(S)-METHYLBUTANAMIDE
BANKS, BJ
BARRETT, AGM
RUSSELL, MA
WILLIAMS, DJ
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1983, (16) : 873 - 875

← 1 2 →