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ChemInform Abstract: 1,4-CHIRALITY TRANSFER VIA THE (2,3)-WITTIG REARRANGEMENT OF THE CHIRAL ALLYLIC PROPARGYL ETHER SYSTEM. A NEW, PRACTICAL ENTRY TO CHIRAL PROPARGYLIC ALCOHOLS
Chemischer Informationsdienst
◽
10.1002/chin.198431159
◽
1984
◽
Vol 15
(31)
◽
Author(s):
N. SAYO
◽
F. SHIRAI
◽
T. NAKAI
Keyword(s):
Chirality Transfer
◽
Wittig Rearrangement
◽
Propargylic Alcohols
◽
System A
◽
Propargyl Ether
◽
Ether System
Download Full-text
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Cited By
References
1,4-CHIRALITY TRANSFER VIA THE [2,3]-WITTIG REARRANGEMENT OF CHIRAL ALLYLIC PROPARGYL ETHER SYSTEM. A NEW, PRACTICAL ENTRY TO CHIRAL PROPARGYLIC ALCOHOLS
Chemistry Letters
◽
10.1246/cl.1984.255
◽
1984
◽
Vol 13
(2)
◽
pp. 255-258
◽
Cited By ~ 16
Author(s):
Noboru Sayo
◽
Fumiyuki Shirai
◽
Takeshi Nakai
Keyword(s):
Chirality Transfer
◽
Wittig Rearrangement
◽
Propargylic Alcohols
◽
System A
◽
Propargyl Ether
◽
Ether System
Download Full-text
ENHANCEMENT OF ERYTHRO-SELECTIVITY IN THE [2,3]-WITTIG REARRANGEMENT OF CROTYL PROPARGYL ETHER SYSTEM AND ITS USE IN THE STEREOCONTROLLED FORMAL SYNTHESIS OF (±)-OUDEMANSIN
Chemistry Letters
◽
10.1246/cl.1983.1379
◽
1983
◽
Vol 12
(9)
◽
pp. 1379-1382
◽
Cited By ~ 21
Author(s):
Koichi Mikami
◽
Ken-ichi Azuma
◽
Takeshi Nakai
Keyword(s):
Formal Synthesis
◽
Wittig Rearrangement
◽
Propargyl Ether
◽
Ether System
Download Full-text
ChemInform Abstract: New Sigmatropic Sequences Based on the I2,3l-Wittig Rearrangement of the Bis-Allylic Ether System: A General Approach to Regiocontrolled C - C Bond Formation of Allylic Moieties Leading to Unsaturated Carbonyl Compounds.
Chemischer Informationsdienst
◽
10.1002/chin.198641125
◽
1986
◽
Vol 17
(41)
◽
Author(s):
K. MIKAMI
◽
N. KISHI
◽
T. NAKAI
◽
Y. FUJITA
Keyword(s):
Carbonyl Compounds
◽
Bond Formation
◽
Wittig Rearrangement
◽
System A
◽
Ether System
Download Full-text
ChemInform Abstract: ENHANCEMENT OF ERYTHRO-SELECTIVITY IN THE (2,3)-WITTIG REARRANGEMENT OF CROTYL PROPARGYL ETHER SYSTEM AND ITS USE IN THE STEREOCONTROLLED FORMAL SYNTHESIS OF (.+-.)-OUDEMANSIN
Chemischer Informationsdienst
◽
10.1002/chin.198409137
◽
1984
◽
Vol 15
(9)
◽
Author(s):
K. MIKAMI
◽
K. AZUMA
◽
T. NAKAI
Keyword(s):
Formal Synthesis
◽
Wittig Rearrangement
◽
Propargyl Ether
◽
Ether System
Download Full-text
Chirality Transfer during the [2,3]-sila-Wittig Rearrangement and Cyclopropanation Reaction of Optically Active [(sec-Allyloxy)silyl]lithiums
Journal of the American Chemical Society
◽
10.1021/ja003749i
◽
2001
◽
Vol 123
(13)
◽
pp. 3143-3144
◽
Cited By ~ 14
Author(s):
Atsushi Kawachi
◽
Hirofumi Maeda
◽
Hiroshi Nakamura
◽
Noriyuki Doi
◽
Kohei Tamao
Keyword(s):
Optically Active
◽
Chirality Transfer
◽
Wittig Rearrangement
Download Full-text
ChemInform Abstract: (2,3)-WITTIG SIGMATROPIC REARRANGEMENT OF CROTYL PROPARGYL ETHER SYSTEM. AN EMERGING TOOL FOR CONTROL OF ACYCLIC STEREOCHEMISTRY
Chemischer Informationsdienst
◽
10.1002/chin.198440090
◽
1984
◽
Vol 15
(40)
◽
Author(s):
K. MIKAMI
◽
K.-I. AZUMA
◽
T. NAKAI
Keyword(s):
Sigmatropic Rearrangement
◽
Propargyl Ether
◽
Ether System
Download Full-text
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: CHIRALITY TRANSFER IN THE (2,3) WITTIG REARRANGEMENT
Chemischer Informationsdienst
◽
10.1002/chin.198447115
◽
1984
◽
Vol 15
(47)
◽
Author(s):
J. A. MARSHALL
◽
T. M. JENSON
Keyword(s):
Chirality Transfer
◽
Wittig Rearrangement
Download Full-text
New sigmatropic sequences based on the [2,3]-wittig rearrangement of the bis-allylic ether system
Tetrahedron
◽
10.1016/s0040-4020(01)90580-0
◽
1986
◽
Vol 42
(11)
◽
pp. 2911-2918
◽
Cited By ~ 19
Author(s):
Kōichi Mikami
◽
Naoyuki Kishi
◽
Takeshi Nakai
◽
Yoshiji Fujita
Keyword(s):
Wittig Rearrangement
◽
Ether System
Download Full-text
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
Download Full-text
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