Stereoselective Synthesis of β-Hydroxyphenylalanines Using Imino 1,2-Wittig Rearrangement of Hydroximates

Okiko Miyata; Hiroshi Asai; Takeaki Naito

doi:10.1248/cpb.53.355

Stereoselective Synthesis of β-Hydroxyphenylalanines Using Imino 1,2-Wittig Rearrangement of Hydroximates

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.53.355 ◽

2005 ◽

Vol 53 (4) ◽

pp. 355-360 ◽

Cited By ~ 7

Author(s):

Okiko Miyata ◽

Hiroshi Asai ◽

Takeaki Naito

Keyword(s):

Stereoselective Synthesis ◽

Wittig Rearrangement

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Stereoselective Synthesis of (±)-Ireland Alcohol Using Titanium-Mediated [2,3]Wittig Rearrangement Product as a Starting Material

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.65.1841 ◽

1992 ◽

Vol 65 (7) ◽

pp. 1841-1848 ◽

Cited By ~ 8

Author(s):

Satoru Ikegami ◽

Hiroaki Okamura ◽

Satoru Kuroda ◽

Tsutomu Katsuki ◽

Masaru Yamaguchi

Keyword(s):

Stereoselective Synthesis ◽

Starting Material ◽

Rearrangement Product ◽

Wittig Rearrangement

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Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic Centers

Chemische Berichte ◽

10.1002/cber.19891220130 ◽

1989 ◽

Vol 122 (1) ◽

pp. 193-198 ◽

Cited By ~ 19

Author(s):

Reinhard Brückner

Keyword(s):

Stereoselective Synthesis ◽

Asymmetric Induction ◽

Wittig Rearrangement ◽

Unsaturated Alcohols ◽

Stereogenic Centers

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[2,3]-Wittig rearrangement of unsymmetrical bis-allylic ethers. Facile method for regio- and stereoselective synthesis of 1,5-dien-3-ols

Journal of the American Chemical Society ◽

10.1021/ja00411a038 ◽

1981 ◽

Vol 103 (21) ◽

pp. 6492-6494 ◽

Cited By ~ 60

Author(s):

T. Nakai ◽

K. Mikami ◽

S. Taya ◽

Y. Fujita

Keyword(s):

Stereoselective Synthesis ◽

Wittig Rearrangement ◽

Allylic Ethers

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Stereoselective Synthesis of β-Hydroxyphenylalanines Using Imino 1,2-Wittig Rearrangement of Hydroximates.

ChemInform ◽

10.1002/chin.200538191 ◽

2005 ◽

Vol 36 (38) ◽

Author(s):

Okiko Miyata ◽

Hiroshi Asai ◽

Takeaki Naito

Keyword(s):

Stereoselective Synthesis ◽

Wittig Rearrangement

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ChemInform Abstract: Chirality Transfer in Stereoselective Synthesis. A Highly Stereocontrolled Synthesis of 22-Hydroxylated Steroid Side Chains via the (2,3)-Wittig Rearrangement.

ChemInform ◽

10.1002/chin.198716339 ◽

1987 ◽

Vol 18 (16) ◽

Author(s):

M. KOREEDA ◽

D. J. RICCA

Keyword(s):

Stereoselective Synthesis ◽

Side Chains ◽

Chirality Transfer ◽

Wittig Rearrangement ◽

Stereocontrolled Synthesis

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ChemInform Abstract: (2,3)-WITTIG REARRANGEMENT OF UNSYMMETRICAL BIS-ALLYLIC ETHERS. FACILE METHOD FOR REGIO- AND STEREOSELECTIVE SYNTHESIS OF 1,5-DIEN-3-OLS

Chemischer Informationsdienst ◽

10.1002/chin.198205087 ◽

1982 ◽

Vol 13 (5) ◽

Author(s):

T. NAKAI ◽

K. MIKAMI ◽

S. TAYA ◽

Y. FUJITA

Keyword(s):

Stereoselective Synthesis ◽

Wittig Rearrangement ◽

Allylic Ethers

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Stereoselective Synthesis of (2Z,4E)-2,4-Pentadien-1-ols via Sequential 1,4-Elimination Reaction and [1,2]-Wittig Rearrangement Starting from (E)-4-Alkoxy-2-butenyl Benzoates

The Journal of Organic Chemistry ◽

10.1021/jo402272r ◽

2013 ◽

Vol 78 (24) ◽

pp. 12654-12661 ◽

Cited By ~ 20

Author(s):

Takeo Nakano ◽

Takahiro Soeta ◽

Kohei Endo ◽

Katsuhiko Inomata ◽

Yutaka Ukaji

Keyword(s):

Stereoselective Synthesis ◽

Elimination Reaction ◽

Wittig Rearrangement

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Highly Stereoselective Synthesis of (E)-Substituted Allylsilanesviathe Still—Wittig Rearrangement

Bioscience Biotechnology and Biochemistry ◽

10.1271/bbb.61.1394 ◽

1997 ◽

Vol 61 (8) ◽

pp. 1394-1396 ◽

Cited By ~ 3

Author(s):

Kazushige Fujii ◽

Osamu Hara ◽

Youji Sakagami

Keyword(s):

Stereoselective Synthesis ◽

Wittig Rearrangement

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Chirality transfer in stereoselective synthesis. A highly stereocontrolled synthesis of 22-hydroxylated steroid side chains via the [2,3]-Wittig rearrangement

The Journal of Organic Chemistry ◽

10.1021/jo00371a042 ◽

1986 ◽

Vol 51 (21) ◽

pp. 4090-4092 ◽

Cited By ~ 26

Author(s):

Masato Koreeda ◽

Daniel J. Ricca

Keyword(s):

Stereoselective Synthesis ◽

Side Chains ◽

Chirality Transfer ◽

Wittig Rearrangement ◽

Stereocontrolled Synthesis

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ChemInform Abstract: Stereoselective Synthesis of (.+-.)-Ireland Alcohol Using Titanium-Mediated (2,3)Wittig Rearrangement Product as a Starting Material.

ChemInform ◽

10.1002/chin.199244290 ◽

2010 ◽

Vol 23 (44) ◽

pp. no-no

Author(s):

S. IKEGAMI ◽

H. OKAMURA ◽

S. KURODA ◽

T. KATSUKI ◽

M. YAMAGUCHI

Keyword(s):

Stereoselective Synthesis ◽

Starting Material ◽

Rearrangement Product ◽

Wittig Rearrangement

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